- Research
- Open access
- Published:
High arsenic contamination in the breast milk of mothers inhabiting the Gangetic plains of Bihar: a major health risk to infants
Environmental Health volume 23, Article number: 77 (2024)
Abstract
Groundwater arsenic poisoning has posed serious health hazards in the exposed population. The objective of the study is to evaluate the arsenic ingestion from breastmilk among pediatric population in Bihar. In the present study, the total women selected were n = 513. Out of which n = 378 women after consent provided their breastmilk for the study, n = 58 subjects were non-lactating but had some type of disease in them and n = 77 subjects denied for the breastmilk sample. Hence, they were selected for the women health study. In addition, urine samples from n = 184 infants’ urine were collected for human arsenic exposure study. The study reveals that the arsenic content in the exposed women (in 55%) was significantly high in the breast milk against the WHO permissible limit 0.64 µg/L followed by their urine and blood samples as biological marker. Moreover, the child’s urine also had arsenic content greater than the permissible limit (< 50 µg/L) in 67% of the studied children from the arsenic exposed regions. Concerningly, the rate at which arsenic is eliminated from an infant’s body via urine in real time was only 50%. This arsenic exposure to young infants has caused potential risks and future health implications. Moreover, the arsenic content was also very high in the analyzed staple food samples such as rice, wheat and potato which is the major cause for arsenic contamination in breastmilk. The study advocates for prompt action to address the issue and implement stringent legislative measures in order to mitigate and eradicate this pressing problem that has implications for future generations.
Introduction
Arsenic a metalloid has become a major environmental toxicant to human population due to its unwanted accumulation in the hydrosphere especially in the groundwater. It is the 20th most abundant heavy metal naturally occurring in the earth crust and also ubiquitously in nature [1]. Due to various geogenic activities like leaching of earth crust ultimately favors the accumulation of arsenic in the groundwater increasing day by day at a very high rate [2]. Other anthropogenic activities also contribute much amount of arsenic in the aquatic system, which ultimately leads to the high contamination of arsenic in the groundwater [3]. Groundwater arsenic poisoning has become a major environmental and health concern worldwide nowadays. It is estimated that about 300 million people worldwide are affected by arsenic poisoning [4, 5]. As determined in Indian population it is seen that 20 States and 4 Union Territories presently have been reported to be affected by arsenic contamination in groundwater comprising 70 million of the total population [5,6,7].
Bihar is a state in Eastern India and is located in Ganga-Meghna-Brahmaputra (GMB) basin. Groundwater is the major source of drinking water in this agrarian state which fulfills more than 80 per cent of drinking source in rural Bihar. Unfortunately, 10 million population of the state are exposed to adverse effects of arsenic poisoning. Out of 38 districts, 22 districts are affected by arsenic poisoning that is more than 50% of the state population [5, 8,9,10,11,12,13,14,15,16,17,18,19,20].
Various studies have been reported with the arsenic poisoning and caused health hazards in the state of Bihar. But these findings are in the arsenic hotspot regions in the middle Ganga plains [5, 7, 19,20,21]. The exposed population exhibit the skin manifestations such as hyperkeratosis, melanosis and pigmentations [10]. The long-term arsenic exposure in these exposed population has also led to the reporting of cancer incidences [5, 22, 23].
Breast milk is a dynamic biological fluid for children and newborns because of its nutritional value as it contains many types of biomolecules such as carbohydrates, proteins, fats, and growth factors and most importantly antibodies [24]. Breast milk is known as the “gold standard” of nourishment to infants. It is made up of distinct elements: 87% as water, with the remainder being macro and micronutrients. It consists of 7% carbs (mostly lactose), 4% fats, 1% proteins, and 1% vitamins and minerals. Colostrum is heavy in protein, vitamins A, B12, and K, as well as oligosaccharides. Arsenic exposure causes accumulation in colostrum milk. Colostrum is primarily used to defend a child’s immune system against many environmental infections [25,26,27,28,29]. Heavy metals such as arsenic, lead, mercury, and cadmium are toxic and its exposure can be of public health concern. These metals cross the placenta and the blood brain barrier, and are excreted through breast milk [30]. Breast milk is the indicator of exposure to heavy metals during prenatal period, it is also exposed to a high risk in breastfed infants during postnatal period [24, 31]. Exposure to heavy metals disturbs the growth and development in newborn and infants [32]. Many studies have reported that infants are more vulnerable than others when they come in contact with heavy metals due to the lack of development of renal systems and lower tolerance level for these contaminants [31, 33,34,35,36,37]. Moreover, this arsenic contamination is majorly contaminating the staple foods such as wheat, rice and potatoes, which is biomagnified and causing health hazards among the exposed population. Hence, the present study aims to find the exposure caused due to the intake of arsenic contaminated drinking water, staple foods such as wheat, rice and potato by the lactating mothers and infants through their mother’s breastmilk intake. Moreover, the study also finds the arsenic contamination in the biological samples of the lactating mothers and to know the carcinogenic risk caused to the infants as well as in their lactating mothers. This exposure study will reveal the results for the first time in the state of Bihar.
Materials and methods
Ethics approval
The Institutional Ethics Committee of the Indian Council of Medical Research Unit- Rajendra Memorial Research Institute of Medical Sciences, Patna, Bihar, India, granted ethical clearance with IEC Letter No. RMRI/EC/24/2020 dated September 26, 2020. Before the investigation began, all patients were briefed about the study’s aims, and signed informed consent was obtained.
Location
The randomly selected habitations were from the 11 arsenic exposed districts- Buxar, Bhojpur, Patna, Saran, Vaishali, Samastipur, Darbhanga, Begusarai, Khagaria, Munger and Nalanda. The study was carried out from the month of October 2021 to May 2023.
Selection of subjects
The population participated in the study were lactating mothers and their breastfeeding infants. In the present study, the total women selected were n = 513. Out of which n = 378 women after consent provided their breastmilk for the study, n = 58 subjects were non-lactating but had some type of disease in them and n = 77 subjects denied for the breastmilk sample. Hence, they were selected for the women health study. Moreover, n = 184 infants (with the age between 0.26 and 30 months) from arsenic exposed population. The studied subjects also provided their biological samples for the evaluation. The information regarding their breastfeeding durations were also accounted through a questionnaire.
Collection of the biological samples
The selected women voluntarily provided breastmilk samples (5 ml), blood samples (5 ml) and their urine samples (50 ml) which was collected in respective containers. The collected samples were stored at 2–6 °C in cool box and then transferred to the research laboratory of Mahavir Cancer Sansthan & Research Centre, Patna, Bihar for further storage at -20 degree Centigrade in deep freezer and was analysed thereafter on Graphite Furnace based Atomic Absorption Spectrophotometer (GF-AAS) of Perkin Elmer model number Pinnacle 900T (USA).
Collection of the household water and food samples
The groundwater samples were collected in 30mL high density polyethylene bottles with a narrow opening. The sample bottles were rinsed and pre-treated with 2% HCl before sampling. The hand pump water source GPS coordinates and their depth related information were recorded. To lower the pH to 2.0, all the water samples were preserved immediately after collection using 1.5 ml/L nitric acid. Moreover, the studied household women also provided their raw food samples such as rice, wheat and potato for the arsenic contamination study. The total arsenic content in the studied institution was evaluated using a Graphite Furnace based Atomic Absorption Spectrophotometer (GF-AAS) of Perkin Elmer model number Pinnacle 900T (USA).
Estimation of breast milk, blood and urine arsenic concentration
For the Breastmilk, blood and urine arsenic estimation, 0·5 ml of samples were taken in 30 ml conical flask (glass) to which, 5 ml of HNO3 were added and left for overnight reaction. The following day, all the samples were digested on hotplate at 90–120 °C, allowing volume to reduce to 3 ml. Then 5 ml volume of HNO3:HClO4 (6:1) mixture were added to the pre-digested solution in the conical flask. The samples were then re-digested on the hotplate at 90 –120 °C, until the volume of the solution reduced to about 2 ml. The final volume was adjusted to 10 ml with addition of distilled water after rinsing it with 1% HNO3 and was then filtered through Whatman filter paper no. 41 for the determination of the final reading on Graphite Furnace Atomic Absorption Spectrophotometer (GF-AAS) (Pinnacle 900T, Perkin Elmer, USA) at the wavelength of 197.3 nm [38, 39].
Ground water arsenic determination
The collected water samples were filtered through the 0.45 μm syringe filter and were directly measured on Graphite Furnace Atomic Absorption Spectrophotometer (GF-AAS) (Pinnacle 900T, Perkin Elmer, USA) at the wavelength of 197.3 nm for total arsenic content [38, 39].
Food sample arsenic determination
The food such as rice, wheat and potato samples in 0.5 g were taken in 25 ml conical flask and to it added 5 ml Conc. HNO3 and left for overnight reaction. The following day the samples were kept on water bath at 60 degree centigrade for 2 h. After the water bath digestion, the samples were allowed to cool at room temperature and then 2 ml of HClO4 was added and then after was heated on hotplate at 1600C for 5 min until the white dense fumes of HClO4 are released. The samples were then cooled at room temperature and the final volume was made by adding 10 ml of demineralized water to the solution. The samples were then filtered with Whatman filter paper No. 41, and were then read through the GF-AAS for arsenic estimation [38, 39].
Quality control
The arsenic standard (1000 mg/L) of PerkinElmer USA (CAS no As7440-38-2; Lot No. 25-127ASY1; PE No N9300180) and standard stock solution was prepared to the point dilution. The calibration correlation coefficient was maintained at 0.999 throughout the analysis period. The detection limit of arsenic in breast milk, blood samples, urine samples and water samples were 0.07 µg/L, 0.09 µg/L, 0.09 µg/L and 10 µg/L respectively. The detection limit of arsenic in food samples such as rice was 0.05 µg/L, wheat as 0.07 µg/L, and potato as 0.05 µg/L respectively. The WHO normal ranges for arsenic contamination in breast milk is 0.64 µg/L, blood − 5 µg/L, urine- 50 µg/L and drinking water is 10 µg/L. For the food samples the FAO normal ranges are- for rice 200 µg/Kg, for wheat 100 µg/Kg and for potato is 500 µg/Kg respectively (Table 1).
The arsenic determination was done with accuracy and precision method. Accuracy is denoted as recovery percentage and precision is denoted as repeatability which is expressed in % relative standard deviation (%RSD). A known amount of arsenic standard was added in the spike samples of water, breast milk, blood, mother’s urine, child’s urine, potato, rice and wheat to determine spike recovery percentage. The recovery percentage of water, breast milk, blood, mother’s urine, child's urine, potato, rice and wheat were 68%, 96.89%, 96%, 84.71%, 85.94%, 95%, 98%, and 97.43% respectively. Repeatability of samples were also calculated by analyzing 5 replicates of each spike samples. The percentage of relative standard deviation of water, breast milk, blood, mother’s urine, child urine, potato, rice and wheat were 0.9%, 1.09%, 0.85%, 2.72%, 0.37%, 2.66%, 0.50%, and 0.92% respectively. All the spike samples were within the limit of accuracy and precision (ISO 17025:2017; ISO 725-2:1994; EPA SW-846) [40,41,42].
Hazard quotient
The hazard quotient represents the non-carcinogenic health risk. There are no negative consequences to the potential or level.
Where,
HQ = Health Quotient.
ADD = Average Daily Dose.
RfD = Oral Reference Dose (0.3 µg/Kg/day) [43].
If the derived HQ value is more than one, a non-carcinogenic impact may be projected; if the determined HQ is one or less than one, no health effect from exposure can be predicted.
Carcinogenic risk (CR)
Carcinogenic risk can be calculated by using this equation.
Where,
CR = Carcinogenic Risk.
ADD = Average Daily Dose.
CSF = Cancer Slope Factor, (1.5 mg/Kg/day).
If CR value is ≤ 1 × 10− 4 then, it is tolerable menace levels.
Spatial analysis
A shape file was constructed by superimposing the GPS coordinates of samples using Arc-GIS Software (10.1). Google map (Google Earth) was utilized as the foundation map. Arsenic concentrations in groundwater, breast milk, blood and urine were classified into three groups. It is expressed in groundwater as BDL (Below Detection Limit), 0–10 µg/L, 11–50 µg/L, 51–100 µg/L, 101–200 µg/L, 201–500 µg/L, > 500 µg/L. It was expressed in blood as BDL (Below Detection Limit), 0–10 µg/L, 11–50 µg/L, 51–100 µg/L, 101–200 µg/L, 201–500 µg/L, > 500 µg/L. It was expressed in breast milk as < 1 µg/L, 1–10 µg/L, 11–50 µg/L, 51–100 µg/L, > 200 µg/L. It was expressed in urine as 0–10 µg/L, 11–50 µg/L, 51–100 µg/L, 101–200 µg/L, 201–500 µg/L, > 500 µg/L. It was expressed in food samples in rice as < 200 µg/Kg, 201–500 µg/Kg, > 500 µg/Kg, in wheat as < 100 µg/Kg, 101–200 µg/Kg, in potato as < 500 µg/Kg, 501–1000 µg/Kg, > 500 µg/Kg.
Statistical analysis
Graph Pad Prism 8.0 and SPSS − 25.0 statistical software were used for the statistical analysis. Arsenic concentrations in groundwater, urine, blood and food samples such as rice, wheat and potato were measured and graphed. With 5 variables, an 8-correlation analysis was performed. The variation across groups was examined using one-way analysis of variance.
Results
Age-wise distribution
The age wise distribution of the subjects inhabiting in the arsenic exposed area depicts that out of total of n = 513 subjects, n = 489 subjects were in the age group between 17 and 40 years, n = 24 subjects were above 40 years (Fig. 1).
Water arsenic concentration
The geospatial maps show significant arsenic contamination in the groundwater in arsenic hotspot 11 districts of Bihar (Fig. 2A). The household water samples of the studied handpumps were in 60–130 feet of depth range. Out of total n = 513 households, n = 450 households had their groundwater arsenic concentration below the permissible limit (10 µg/L) [44, 45]. Hence, the study interprets that most of the groundwater samples was safe for drinking. However, the highest arsenic concentration in the groundwater found was 550.7 µg/L (Fig. 2B).
Blood arsenic concentration
The geospatial maps show significant arsenic content in the blood samples of the subjects in arsenic hotspot 11 districts of Bihar (Fig. 3A). There was significant blood arsenic contamination observed in n = 205 subjects. The study showed that n = 84 subjects had their blood arsenic concentration below 10 µg/L. About n = 121 subjects had arsenic contamination in their blood above the permissible limit of 10 µg/L with the highest content as 732 µg/L (Fig. 3B). This denotes that major chunk of studied subjects had their arsenic content in blood above the permissible limit of 10 µg/L [46].
Breastmilk arsenic concentration
The geospatial maps show significant arsenic content in the breast milk samples of the subjects in arsenic hotspot 11 districts of Bihar (Fig. 4A). The arsenic contamination study in breastmilk was carried out in n = 378 subjects. The study showed that n = 168 subjects had their breastmilk arsenic content below the permissible level, while n = 210 subjects had arsenic content in their breastmilk more than the permissible limit < 1 µg/L [47]. The highest arsenic content in the breastmilk was 458 µg/L (Fig. 4B). The correlation coefficient between mother’s breast milk with mother’s urine (r2 = 0.562) and its comparison with breastmilk and child’s urine (r2 = 0.287) shows mild correlation (Fig. 4C). This denotes that arsenic exposure is caused to the infants is through their mother’s breast milk.
Mother’s urine arsenic concentration
The geospatial maps show significant arsenic contamination in the mother’s urine samples of the subjects in arsenic hotspot 11 districts of Bihar (Fig. 5A). The estimation of urine arsenic content was carried out in n = 461 in the arsenic exposed subjects. The study showed that n = 92 subjects had their urine arsenic content below the permissible level (50 µg/L) [48], while n = 369 subjects had arsenic content in their urine more than the permissible limit. The highest arsenic content in the urine was 1039 µg/L (Fig. 5B). The Hazard Quotient study shows significant arsenic exposure association with a higher non-carcinogenic risk in the lactating mothers (Fig. 5C), (Table 1, Supplement-1; table 2, Supplement-2). This denotes that the subjects are at very high risk of cancer in future due to long term arsenic exposure.
Child’s urine arsenic concentration
The geospatial maps show significant arsenic content in the child’s (infants) urine samples in the arsenic hotspot 11 districts of Bihar (Fig. 6A) with illustration showing the reason behind the arsenic poisoning in this particular region (Fig. 6B). The estimation of child’s urine arsenic content was carried out in n = 184 in the arsenic exposed subjects. The study showed that n = 60 child subjects had their urine arsenic concentration below the permissible level (50 µg/L) [48], while n = 124 child subjects had arsenic content in their urine more than the permissible limit. The highest arsenic content in the urine was 1031 µg/L (Fig. 6C). The Hazard Quotient study shows significant arsenic exposure association with a higher non-carcinogenic risk in the infants (Fig. 6D). It is possible that children’s smaller body weight contributes to the higher risk they face as a group. On the other hand, each sample had a Carcinogenic Risk (CR) that was higher than the threshold value of 1 × 10− 6 in the children population group, whereas the threshold value was found to be lower in the population group of nursing mothers (Table 1, Supplement-1; Table 2, Supplement-2). The possible reason of high arsenic content in the child’s urine is their mother’s contaminated breast milk.
Rice arsenic concentration
The geospatial maps show significant arsenic contamination in the rice samples of the subjects in arsenic hotspot 11 districts of Bihar (Fig. 7A). The arsenic content study in rice samples were carried out in n = 369 in the arsenic exposed population. The study showed that n = 319 households had their rice arsenic content below the permissible level, while n = 50 households had arsenic content in their rice samples more than the permissible limit (< 200 µg/Kg) [49]. The highest arsenic content in the rice was 821 µg/Kg (Fig. 7B).
Wheat arsenic concentration
The geospatial maps show significant arsenic content in the wheat samples of the subjects in arsenic hotspot 11 districts of Bihar (Fig. 8A). The arsenic content study in wheat was carried out in n = 279 in the arsenic exposed population. The study showed that n = 105 households had their wheat arsenic concentration below the permissible level, while n = 174 households had arsenic content in their wheat samples more than the permissible limit (< 100 µg/Kg) [49]. The highest arsenic content in the wheat sample was 775 µg/Kg (Fig. 8B).
Potato arsenic concentration
The geospatial maps show significant arsenic contamination in the potato samples of the subjects in arsenic hotspot 11 districts of Bihar (Fig. 9A). The arsenic content study in potato samples was carried out in n = 168 in the arsenic exposed population. The study showed that n = 163 households had their potato arsenic concentration below the permissible level, while n = 5 households had arsenic content in their potato more than the permissible limit (< 500 µg/Kg) [49]. The highest arsenic content in the potato was 1450 µg/Kg (Fig. 9B).
Human health risk assessment
The groundwater arsenic concentration and breast milk arsenic concentration is used for the estimation of health risk assessment of mother’s and children population respectively. The results reveal that 37.23% samples of ground water and 97.08% samples of breast milk exceeded the threshold limit of hazard quotient. It means 37.23% mother’s population and 97.08% of children have potential risk of non-carcinogenic health effect. If the carcinogenic risk is taken in account, then it was found that, 85.96% of ground water samples and 98.41% of breast milk samples have crossed the limit of ILCR (Incremental lifetime cancer risk) which indicates that 85.96% of mother’s and 98.41% of children is on the verge of causing cancer in the near future (Fig. 10; Table 2).
Geological perspective
From the geological perspective, as depicted on the map of Bihar (Fig. 1A, amp and B, 2 A&B, 3 A&B, 4 A&B, 5 A, 6 A, 7 A and 8 A), the alarming hotspots whether in groundwater, mother’s milk or urine or the food samples are defining the regions from where the samples have been collected show a definitive proximity to the Gangetic flow regime on either of its bank. It is clearly the oscillation zone of river Ganga which is defined by the conspicuous crests and troughs perpendicular to its flow and is what defines the pockets of moderate to high arsenic contamination. Arguably the river morphology has seen a remarkable change temporally and has thus influenced areas which at one point in time during the last 50 years of reference were not as much affected. Thus, Ganga River continues to act as an extensive receptacle of sediments which based on river morphology, change in channel architecture, and effect of biological activity has clearly accentuated the anomalous concentration level within aquifers and the sediments accumulating along this zone. With the belief that the arsenic laden sediments are primarily derived from the extra peninsula region, the levels of contamination are significantly higher within the oscillation zone of Ganga River than the districts in north Bihar which are presumably closer to the source of contamination. Whether in Darbhanga or Champaran district of Bihar (based on studies carried out by Geological Survey of India), the level of contamination is not as high as that found within the flow regime of River Ganga where most of these rivers draining the Himalayas make a confluence with the larger order stream [50, 51]. Thus, the arsenic exposed area of Bihar vouches the alarming concentration within breastmilk, blood, urine or groundwater samples.
A few high values have been observed within the non-arsenic affected districts as well and which need to be examined from the geological perspective. Figure 5B indicates that out of 15 water samples collected from Nalanda, Gaya and Jehanabad district (primarily non arsenic affected areas), none of the results show a concentration beyond 10 ppb which supports the observation of aquifers being free of arsenic contamination. But, as per Fig. 2D (blood sample) Fig. 3D (breast milk) and Fig. 4D (urine sample), there are only a few instances where the human body parameters show increased levels. Understanding the area of interest geologically, the sampled area to the north of NE-SW trending Rajgir hills is occupied by rocks constituting the volcano sedimentary sequence. The Rajgir hills represents the Rajgir-Munger metasediments formed under lacustrine conditions comprising quartzites and phyllites which overlain the basement rocks i.e. the granites and its variants. Principally, they aren’t a proven source for arsenic based on their mineralogical constitution. But, the volcano sedimentary package reveals emplacement of diverse mafic and felsic rocks and they together justify for multistage and multi-source magmatism in the area. The presence of pillow lava marks the eruption of these rocks in subaqueous environment [52, 53] (Fig. 9. Supplement 3).
The occurrence of a lithological setup as diverse as these advocates for an upwelling mechanism which are derivative of volcanic rocks as they appear on the surface. The area also coincides with the trace of the Munger Saharsa Ridge Fault aligned with the northern faulted face of Rajgir hills along which several hotsprings are located and they derive gases from some hot unknown magmatic source. These volcanic rocks may have derived some arsenic rich plumes defining multistage and multi-source magmatism in the area which ideally are confined to this zone only [54, 55].
But this hypothesis cum observation has to be affirmed by extensive sampling in the area of various available media viz. rocks, water (from aquifers at various depths) soil and stream sediments to affirm this observation as the water samples do not have anomalous concentration. The few cases which have yielded high levels in mother’s milk, blood or urine could also have migrated from arsenic affected areas recently or post contamination. With earth’s crust containing (on average) 1.5ppm arsenic, it is unlikely to be the direct source for increased concentration if not supported by prevalence of arsenic bearing minerals [56].
Discussion
Environmental pollutants are posing severe health threats to the humans. Infants are more vulnerable to these pollutants. Arsenic in the recent times in the Gangetic plains of Bihar has shown severe health hazards in the exposed population. Most of the studies carried out are on the adults, but the present study reveals for the first time the impact of arsenic exposure on the infants in the Gangetic plains of Bihar. In the present study, the maximum age group in arsenic exposed subjects were observed in 85% of the subjects with the age group between 17 and 30 years, while 15% subjects were in the age group between 31 and 60 years. The arsenic concentration, in studied n = 513 water samples, 88% water samples had arsenic concentration below the WHO levels of 10 µg/L. Only 12% water samples had arsenic concentration in water samples between 11 and 550 µg/L with maximum concentration as 551 µg/L. The blood arsenic concentration in the studied arsenic exposed subjects in n = 205 samples, 41% had the blood arsenic content in the normal range that is below 10 µg/L, while 59% blood samples had arsenic content above the permissible limit with highest content as 732 µg/L. The reason for the excessive arsenic content in their blood is due to the intake of staple foods such as rice, wheat and potato which were contaminated with arsenic. The breastmilk arsenic content in arsenic exposed population in the studied n = 378 subjects, 44% subjects had arsenic content below permissible limit that is < 1 µg/L, while 56% subjects had arsenic content above the permissible limit with highest arsenic content as 458 µg/L. In the studied mother’s urine arsenic concentration in arsenic exposed population in n = 461 subjects, 20% had arsenic content below permissible limit of 50 µg/L. However, 80% subjects had arsenic content in their urine above the permissible limit with maximum arsenic concentration as 1038 µg/L. In the child’s urine arsenic concentration studied carried out in arsenic exposed n = 184 child subjects, 33% child subjects had arsenic content in their urine below permissible limit (50 µg/L), while 67% child subjects had arsenic content above permissible limit with maximum arsenic concentration as 1031 µg/L.
In the studied food samples in the rice, the arsenic concentration in the studied 369 rice samples, 86% had arsenic content below FAO permissible limit of 200 µg/Kg [57]. However, 14% rice samples had arsenic content above the permissible limit with maximum arsenic concentration as 821 µg/Kg. In the studied food samples in the wheat, the arsenic concentration in the studied 279 wheat samples, 37% had arsenic content below FAO permissible limit of 100 µg/Kg [58]. However, 63% wheat samples had arsenic content above the permissible limit with maximum arsenic concentration as 775 µg/Kg. In the studied food samples in the potato, the arsenic concentration in the studied 168 potato samples, 97% had arsenic content below FAO permissible limit of 500 µg/Kg [49] However, 3% potato samples had arsenic content above the permissible limit with maximum arsenic concentration as 1450 µg/Kg.
The biomagnification of the arsenic contamination in the studied humans through the intake of their food samples is the first finding ever reported in these 11 districts of Bihar. Moreover, the major chunk of the population is at very high risk as they are consuming arsenic contaminated food, which through the breast milk is reaching to their infants. From the results, it reveals that in the arsenic exposed population inhabiting in the districts along the river Ganges – Buxar, Bhojpur, Saran, Patna, Vaishali, Samastipur, Beugusarai, Khagaria, Nalanda, Darbhanga and Munger are at the verge of high risk of disease burden. The infants are at very high risk for the disease burden in the future as their mothers are lactating high arsenic content in their breast milk. This can lead to mental disorders, low intelligence, low memory etc. in these infants. Rebelo & Caldas, 2016 have studied the toxic effects of arsenic, lead, mercury and cadmium in breast milk and risks caused to the breastfed infants in Brazil [24]. Furthermore, the study also depicted that there is no safe dose of exposure established for arsenic or lead. Mohammadi et al., 2022 studied the contamination of breast milk with arsenic, lead, mercury and cadmium in Iran and reported that these toxic heavy metals had high content in the milk colostrum [59]. Freire et al., 2022 reported high heavy metal such as arsenic, mercury, lead and cadmium content in pooled donor breast milk in Spain [60]. Sharafi et al., 2023 reported high arsenic content in 73% of studied lactating mother’s breastmilk in Iran [61]. The calculated HQ was also very high in the studied infants due to arsenic toxicity caused through breastmilk. Salmani et al., 2018 studied the arsenic exposure in breast fed infants in the first month after their birth in Iran in the study 53% of lactating mother’s breastmilk was contaminated with arsenic [33]. Bassil et al., 2018 reported 63% of lactating mother’s breastmilk contaminated with arsenic in Lebanon [62]. The arsenic exposure was found to be through the cereal and fish intake by the exposed population. Similar other studies were also reported from the studied countries China, Iran, Turkey, Germany and India [63,64,65,66,67,68].
This study carried out in Iran, evaluated the concentrations of lead (Pb), arsenic (As), and chromium (Cr) in the breast milk of 100 urban mothers in the city Hamadan, and assessed the associated health risks for infants. Breast milk samples were collected at 2, 6, 8, and 12 months postpartum, with heavy metal concentrations measured. The median concentrations of Pb, As, and Cr were 41.90, 0.50, and 3.95 µg/L, respectively. Notably, 94% of samples exceeded the WHO lead contamination limit. The hazard quotient (HQ) for Pb and arsenic exceeded acceptable levels in 61% and 10% of samples, respectively, indicating a potential health risk for infants [69]. Another cross-sectional study carried out in Iran, studied breast milk from 100 healthy lactating mothers in Hamadan city, focused on aluminum and various minerals and trace elements. Samples were collected at 1, 2, 6, 7, and 12 months postpartum from ten government health centers. The study reported levels of sodium, zinc, calcium, iron, copper, magnesium, and aluminum. The mean concentrations were 0.75 µg/mL for iron, 1.38 µg/mL for zinc, and 0.191 µg/mL for aluminium, with 95% of participants showing harmful levels of aluminum. Additionally, zinc deficiency was observed in 50% of samples, highlighting potential health risks [70]. Another study from Iran, carried out the exposure study of toxic metals. This systematic review assessed the risks of arsenic in breast milk for newborns and infants. In the study, the arsenic levels ranged from 0.04 ± 0.70 to 27.75 ± 28.30 µg/L, with a pooled average concentration of 0.11 µg/L, suggesting that infant breast milk consumption poses a minimal cancer risk [71].
According to the findings of this research, it is abundantly evident that the presence of these heavy metals is evidence that mothers are exposed to arsenic poisoning. This not only has a detrimental effect on the health of the infant, but it also has a detrimental effect on the health of the mother as well. It was discovered that prolonged exposure to arsenic in newborns or children up to the age of 5, may result in decreased intellectual quotient (IQ) scores. This was discovered via observation. There have been reports that various arsenic concentrations have been discovered [72]. In 55% of the breastmilk samples, the amount of arsenic was more than the WHO permitted limit of < 1 µg/L, in the mothers inhabiting the arsenic exposed region. Similar study was conducted in West Bengal (India) where mothers were lactating arsenic contaminated breast milk and were feeding to their infants unknowingly [73]. Due to the fact that arsenic may be taken up by plants via the soil’s surface, it is also possible to assert that food crops, in addition to drinking water, should be regarded as an essential means by which individuals take in arsenic [74]. Previous research has shown that irrigating food crop plants with water containing arsenic may make the soil more likely to retain arsenic via the adsorption of arsenic on soil exchange complexes [75]. In the present study, the high arsenic content in the rice and wheat denotes that through the food chain the arsenic biomagnification has taken place in the mothers which in turn are lactating high arsenic contaminated breastmilk which are fed by their infants accidentally. Infants who are vulnerable to the effects of arsenic exposure via drinking water are an additional factor that might be regarded a significant source. There is evidence that the transmission of arsenic to the mammary glands is reduced, which ultimately protects the neonates from being exposed to arsenic [76, 77]. It has also been claimed that the foetus and babies are protected from arsenic exposure owing to arsenic methylation when the mother is pregnant and while the mother is nursing the baby [50, 78]. But, in contrast to these studies, no studies have reported the real time arsenic poisoning in the children in the Gangetic plains of Bihar (India). The present study clearly reports that in 55% of the exposed lactating mothers had arsenic content in their breastmilk higher than the WHO permissible limit. The same day child’s urine arsenic content was also observed in 65% of the arsenic exposed children. The study throws light that the mothers who lactated the arsenic in their breast milk and same day only 50% of the arsenic was released through the child’s urine. This denotes that the rest 50% of the arsenic is accumulated in the child’s body and could be highly toxic to the vital organs of the body such as brain, liver, kidney, heart, lungs etc. Moreover, the child’s day to day activity will also be in catastrophic condition, which needs to be catered through the medical interventions.
The geological perspectives also report that arsenic poisoning in the subjects in the Gangetic plains of Bihar is due to the oscillation movement of river Ganga along its course. The studied districts were Buxar, Bhojpur, Patna, Saran, Samastipur, Begusarai, Khagaria, Munger, Nalanda and Darbhanga. The selected district Nalanda was thought to be arsenic free region of the state, but this study reveals for the first time the arsenic poisoning in the exposed population. Moreover, the strong hypothesis related to the tectonic movements in the Rajgir hills area, clearly demonstrates the presence of arsenic in the sediments as well as in the water [50, 51]. In the present study the high arsenic content in the breastmilk of the exposed population of the districts of Bihar was found to be in the following increasing order Khagaria > Saran > Begusarai > Samastipur > Buxar > Bhojpur > Darbhanga > Munger > Vaishali > Patna > Nalanda.
The hazard quotient study carried also correlates that the infants are more vulnerable to carcinogenic risk followed by their lactating mothers. This risk study also correlates that arsenic poisoning is directly correlated to the child’s arsenic poisoning [43, 51, 79,80,81]. This could further worsen the basic activities, growth, mental growth of the child with the growing age. Hence, there is urgent intervention required to combat the problem in the exposed population especially the lactating mothers and their infants.
Conclusions
The present study concludes that arsenic poisoning is prevalent in the Gangetic plains of Bihar in the studied districts - Buxar, Bhojpur, Patna, Saran, Samastipur, Begusarai, Khagaria, Munger, Darbhanga and Nalanda. The study reports for the first time in these studied districts of Bihar with arsenic poisoning in the biological samples of the lactating mother as well as in their infants. The study demonstrates a direct correlation between contaminated breast milk and infant arsenic toxicity. This could result in substantial health risks for both mothers and infants, as it could harm the development of their children. In addition, neonates who consumed arsenic through their mother’s breast milk eliminated only 50% of the arsenic content, while the remaining arsenic content accumulated in their bodies, posing serious health risks. The carcinogenic risk was also very high in the exposed infants followed by their mothers. Therefore, it is essential to implement medical intervention urgently in order to address the current problems. The mothers can be awared for using arsenic free water and food which can prevent her from exposure of arsenic & child through breastmilk. The formulation of health policies by the state government is necessary to mitigate the risk of exacerbated health conditions in newborns who have been exposed to arsenic poisoning.
Data availability
Data is provided within the manuscript or supplementary information files.
References
Mandal BK, Suzuki KT. Arsenic round the world: a review. Talanta. 2002;58(1):201–35.
Devi P, Singh P, Kansal SK, editors. Inorganic pollutants in water. Elsevier; 2020.
Rehman MU, Khan R, Khan A, Qamar W, Arafah A, Ahmad A, Ahmad A, Akhter R, Rinklebe J, Ahmad P. Fate of arsenic in living systems: implications for sustainable and safe food chains. J Hazard Mater. 2021;417:126050. https://doi.org/10.1016/j.jhazmat.2021.126050.
Hassan MM. Arsenic in groundwater: poisoning and risk assessment. Crc; 2018.
Kumar A, Ali M, Kumar R, Kumar M, Sagar P, Pandey RK, Akhouri V, Kumar V, Anand G, Niraj PK, Rani R, Kumar S, Kumar D, Bishwapriya A, Ghosh AK. (2021a). Arsenic exposure in Indo Gangetic plains of Bihar causing increased cancer risk. Sci Rep, 11(1), 2376. https://doi.org/10.1038/s41598-021-81579-9.
Shaji E, Santosh M, Sarath KV, Prakash P, Deepchand V, Divya BV. Arsenic contamination of groundwater: a global synopsis with focus on the Indian Peninsula. Geosci Front. 2021;12(3):101079.
Kumar A, Rahman MS, Ali M, Salaun P, Gourain A, Kumar S, Kumar R, Niraj PK, Kumar M, Kumar D, Bishwapriya A, Singh S, Murti K, Dhingra S, Sakamoto M, Ghosh AK. Assessment of disease burden in the arsenic exposed population of Chapar village of Samastipur district, Bihar, India, and related mitigation initiative. Environ Sci Pollut Res Int. 2022;29(18):27443–59. https://doi.org/10.1007/s11356-021-18207-6.
Kumar A, Kumar R, Rahman MS, Ali M, Kumar R, Nupur N, Gaurav A, Raj V, Anand G, Niraj PK, Kumar N, Srivastava A, Biswapriya A, Chand GB, Kumar D, Rashmi T, Kumar S, Sakamoto M, Ghosh AK. (2021b). Assessment of arsenic exposure in the population of Sabalpur village of Saran District of Bihar with mitigation approach. Environ Sci Pollut Res Int, https://doi.org/10.1007/s11356-021-13521-5. Advance online publication.
Kumar A, Rahman MS, Ali M, Kumar R, Niraj PK, Akhouri V, Singh SK, Kumar D, Rashmi T, Bishwapriya A, Chand GB, Sakamoto M, Ghosh AK. (2021c). Assessment of arsenic exposure and its mitigation intervention in severely exposed population of Buxar district of Bihar, India. Toxicol Environ Health Sci. https://doi.org/10.1007/s13530-021-00086-6.
Kumar A, Ghosh AK. (2021). Assessment of arsenic contamination in groundwater and affected population of Bihar. N. Kumar, editor, Arsenic Toxicity: Challenges and Solutions. [ISBN 978-981-33-6067-9; ISBN 978-981-33-6068-6 (eBook)] https://doi.org/10.1007/978-981-33-6068-6_7
Kumar A, Ali M, Kumar R, Rahman MS, Srivastava A, Chayal NK, Sagar V, Kumari R, Parween S, Kumar R, Niraj PK. High arsenic concentration in blood samples of people of village Gyaspur Mahaji, Patna, Bihar drinking arsenic-contaminated water. Exposure Health. 2020;12:131–40.
Kumar A, Ghosh AK. Arsenic and Cancer. Environmental Exposures and Human Health Challenges. IGI Global; 2019. pp. 106–32.
Rahman MS, Kumar A, Kumar R, Ali M, Ghosh AK, Singh SK. (2019a). Comparative Quantification Study of Arsenic in the Groundwater and Biological samples of Simri Village of Buxar District, Bihar, India. Indian J Occup Environ Med 23(3):126–32. https://doi.org/10.4103/ijoem.IJOEM_240_18.
Rahman MS, Kumar A, Kumar R, Ali M, Ghosh AK, Singh SK. (2019b). Hematological and free radicals changes among people of arsenic endemic region of Buxar District of Bihar, India. Int J Pub Health Safe, 4(178), 2.
Abhinav A, Navin S, Kumar A, Kumar R, Ali M, Verma SK, Ghosh AK. Prevalence of high arsenic concentration in Darbhanga district of Bihar: health assessment. J Environ Anal Toxicol. 2016;6(410):2161–0525.
Abhinav NS, Shankar P, Kumar R, Ali M, Verma SK, Ghosh AK, Kumar A. Arsenic contamination of groundwater and human blood in Vaishali district of Bihar, India: health hazards. Int J Adv Res. 2017;5(8):2092–100.
Chakraborti D, Singh SK, Rahman MM, Dutta RN, Mukherjee SC, Pati S, Kar PB. Groundwater Arsenic Contamination in the Ganga River Basin: a Future Health Danger. Int J Environ Res Public Health. 2018;15(2):180. https://doi.org/10.3390/ijerph15020180.
Eikelboom M, Wang Y, Portlock G, Gourain A, Gardner J, Bullen J, Salaun P. Voltammetric determination of inorganic arsenic in mildly acidified (pH 4.7) groundwaters from Mexico and India. Anal Chim Acta. 2023;341589. https://doi.org/10.1016/j.aca.2023.341589.
Richards LA, Kumari R, White D, Parashar N, Kumar A, Ghosh A, Kumar S, Chakravorty B, Lu C, Civil W, Lapworth DJ, Krause S, Polya DA, Gooddy DC. Emerging organic contaminants in groundwater under a rapidly developing city (Patna) in northern India dominated by high concentrations of lifestyle chemicals. Environ Pollution (Barking Essex: 1987). 2021;268Pt A:115765. https://doi.org/10.1016/j.envpol.2020.115765.
Richards LA, Kumar A, Shankar P, Gaurav A, Ghosh A, Polya DA. Distribution and geochemical controls of arsenic and uranium in groundwater-derived drinking water in Bihar, India. Int J Environ Res Public Health. 2020;17(7):2500.
Richards LA, Kumari R, Parashar N, Kumar A, Lu C, Wilson G, Lapworth D, Niasar VJ, Ghosh A, Chakravorty B, Krause S, Polya DA, Gooddy DC. Environmental tracers and groundwater residence time indicators reveal controls of arsenic accumulation rates beneath a rapidly developing urban area in Patna, India. J Contam Hydrol. 2022;249:104043. https://doi.org/10.1016/j.jconhyd.2022.104043. Advance online publication.
Kumar, A., Ali, M., Raj, V., Kumari, A., Rachamalla, M., Niyogi, S., Kumar, D., Sharma,A., Saxena, A., Panjawani, G., Jain, P., Vidyarthi, A., Kumar, N., Kumar, M., Niraj,P. K., Rahman, M. S., Bishwapriya, A., Kumar, R., Sakamoto, M., Kumar, S., … Ghosh,A. K. (2023). Arsenic causing gallbladder cancer disease in Bihar. Scientific reports,13(1), 4259. https://doi.org/10.1038/s41598-023-30898-0.
Kumar A, Kumar K, Ali M, Raj V, Srivastava A, Kumar M, Niraj PK, Kumar M, Kumar R, Kumar D, Bishwapriya A, Kumar R, Kumar S, Anand G, Kumar S, Sakamoto M, Ghosh AK. Severe Disease Burden and the Mitigation Strategy in the Arsenic-exposed Population of Kaliprasad Village in Bhagalpur District of Bihar, India. Biol Trace Elem Res. 2023. https://doi.org/10.1007/s12011-023-03822-w. Advance online publication.
Abboud AH, Almayahi BA. Relationship between heavy metals and alpha emission rates in breast milk and blood of women. Heliyon. 2021;7(3):e06590. https://doi.org/10.1016/j.heliyon.2021.e06590.
Andreas NJ, Kampmann B, Mehring Le-Doare K. Human breast milk: a review on its composition and bioactivity. Early Hum Dev. 2015;91(11):629–35. https://doi.org/10.1016/j.earlhumdev.2015.08.013.
Emmett PM, Rogers IS, Suppl. 7–S28. https://doi.org/10.1016/s0378-3782(97)00051-0.
Gomez-Gallego C, Garcia-Mantrana I, Salminen S, Collado MC. The human milk microbiome and factors influencing its composition and activity. Semin Fetal Neonatal Med. 2016;21(6):400–5. https://doi.org/10.1016/j.siny.2016.05.003.
Mandal SM, Bharti R, Porto WF, Gauri SS, Mandal M, Franco OL, Ghosh AK. Identification of multifunctional peptides from human milk. Peptides. 2014;56:84–93. https://doi.org/10.1016/j.peptides.2014.03.017.
Matos C, Ribeiro M, Guerra A. Breastfeeding: antioxidative properties of breast milk. J Appl Biomed. 2015;13(3):169–80.
Rebelo FM, Caldas ED. Arsenic, lead, mercury and cadmium: toxicity, levels in breast milk and the risks for breastfed infants. Environ Res. 2016;151:671–88. https://doi.org/10.1016/j.envres.2016.08.027.
Al-Saleh I. Health Risk Assessment of Trace Metals through Breast Milk Consumption in Saudi Arabia. Biol Trace Elem Res. 2021;199(12):4535–45. https://doi.org/10.1007/s12011-021-02607-3.
Szukalska M, Merritt TA, Lorenc W, Sroczyńska K, Miechowicz I, Komorowicz I, Mazela J, Barałkiewicz D, Florek E. Toxic metals in human milk in relation to tobacco smoke exposure. Environ Res. 2021;197:111090. https://doi.org/10.1016/j.envres.2021.111090.
Salmani MH, Rezaie Z, Mozaffari-Khosravi H, Ehrampoush MH. Arsenic exposure to breast-fed infants: contaminated breastfeeding in the first month of birth. Environ Sci Pollut Res Int. 2018;25(7):6680–4. https://doi.org/10.1007/s11356-017-0985-z.
Mahdavi R, Nikniaz L, Arefhosseini S, Jabbari MV. Determination of aflatoxin M1 in breast milk samples in Tabriz– Iran. Maternal Child Health J. 2010;14(1):141–5. https://doi.org/10.1007/s10995-008-0439-9.
Yasaei MGR, Ezzatpanah H, Yasini AS, Dadfarnia S. Assessment of lead and cadmium levels in raw milk from various regions in Yazd province. J Food Technol Nut. 2010;7:35–42.
Malakootian M, Golpayegani A. Determination of Pb, Cd, Al, Zn and ca in infant formula and baby foods in Iran and estimation of daily infant intake of these metals. Iran J Nut Sci Food Technol. 2013;8:251–9.
Hojsak I, Braegger C, Bronsky J, Campoy C, Colomb V, Decsi T, Domellöf M, Fewtrell M, Mis NF, Mihatsch W, Molgaard C, van Goudoever J, ESPGHAN Committee on Nutrition. Arsenic in rice: a cause for concern. J Pediatr Gastroenterol Nutr. 2015;60(1):142–5. https://doi.org/10.1097/MPG.0000000000000502.
NIOSH Manual of Analytical Methods, 2nd. ed., V. 1, P&CAM 139, U.S. Department of Health, Education, and Welfare, Publ. (NIOSH) 77-157-A. (1977).
Criteria for a Recommended Standard… Occupational Exposure to Inorganic Arsenic, U.S.Department of Health, Education, and Welfare, Publ. (NIOSH) 75–149 (1975).
International Organization for Standardization. ISO/IEC 17025:2017 – general requirements for the competence of testing and calibration laboratories. ISO; 2017.
International Organization for Standardization. ISO 5725-2:1994 - accuracy (trueness and precision) of measurement methods and results - part 2: basic method for the determination of repeatability and reproducibility of a standard measurement method. ISO; 1994.
U.S. Environmental Protection Agency. (2015). Test methods for evaluating solid waste, physical/chemical methods (SW-846). U.S. EPA. https://www.epa.gov/hw-sw846
USEPA (United States Environmental Protection Agency). 2014. Human Health Evaluation Manual, Supplemental Guidance: Update of Standard Default Exposure Factors-OSWER Directive 9200.1–120. PP.6.
WHO. (2018). Arsenic. Geneva, World Health Organization (WHO Fact Sheet; https://www.who.int/en/news-room/fact-sheets/detail/arsenic)
WHO. (2017). Guidelines for drinking-water quality, 4th edition incorporating the first addendum. Geneva, World Health Organization, pp. 315–318 (https://apps.who.int/iris/bitstream/handle/10665/254637/9789241549950-eng.pdf).
ATSDR. (2007). Agency for Toxic Substances and Disease Registry. U.S. Department of Health and Human Services, Public Health Service. Toxicological profile for Arsenic. Available: http://www.atsdr.cdc.gov/toxprofiles/tp2.pdf
Bartmess JE. Minor and Trace elements in breast milk: report of a Joint WHO/IAEA Collaborative Study. J Hum Lactation. 1990;6(1):28–9. https://doi.org/10.1177/089033449000600125.
Centers for Disease Control and Prevention (CDC). National Health and Nutrition Examination Survey. 2004. http:/www.cdc.gov/nchs/nhanes.htm accessed on April 2 2008.
FAO; WHO. (2011) Working document for information and use in discussions related to contaminants and toxins in the GSCTFF. In: Codex Committee on Contaminants in Foods. Fifth Session. The Hague: FAO; 2011. 89p.
GSI. (2020). Final report on geological assessment of incidence of arsenic in groundwater around Biraul, Baheri, Kusheshwarsthan (E and W), alinagar and adjoining areas in Darbhanga district, Bihar. Geological Survey of India report, unpublished report (FS:2018-19 & 2019-20).
GSI. (2022). Geological assessment of Incidence of Arsenic in groundwater around Harnatar, Nautanwa, Bagaha, Bhairoganj and adjoining areas West Champaran district, Bihar. Geological Survey of India report, unpublished report (FS:2021-22).
Ahmad M, Paul AQ. (2012). Tectono-stratigraphic constraints of the Bathani volcano-sedimentary, volcanic sequences and associated rocks, Chotanagpur granite gneiss complex, Gaya district, Bihar. NEWS Geol. Surv. India, Eastern region, 33, 13–15.
Ahmad M, Paul AQ. Investigation of volcano-sedimentary sequence and associated rocks to identify gold and base metal mineralization at Gere-Kewti area of Gaya District, Bihar (G4). Bangalore: Unpublished Report Geological Society of India; 2013.
Saikia A, Gogoi B, Ahmad M, Ahmad T. Geochemical constraints on the evolution of mafic and felsic rocks in the Bathani volcanic and volcano-sedimentary sequence of Chotanagpur Granite Gneiss Complex. J Earth Syst Sci. 2014;123:959–87.
Saikia A, Gogoi B, Kaulina T, Lialina L, Bayanova T, Ahmad M. Geochemical and U–Pb zircon age characterization of granites of the Bathani Volcano sedimentary sequence, Chotanagpur Granite Gneiss Complex, eastern India: vestiges of the Nuna supercontinent in the Central Indian Tectonic Zone. Geol Soc Lond Special Publications. 2017;4571:233–52.
Taylor SR, Mclennan SM. The geochemical evolution of the continental-crust. Rev Geophys. 1995;33:241–65.
Åkesson MT, Point CC, di Caracalla VDT. Joint FAO/WHO food standards programme codex committee on contaminants in foods. Geneva: WHO; 2015.
Elsheery NI, Mohamed N, Helaly, Sahar F, El-Hefnawy MM, Elhamahmy EM, Abdelrazik YB, Sardarov, Parvaiz Ahmad, Marek Zivcak, Marian Brestic, and, Suleyman I, Allakhverdiev. (2023). 5-Aminolevulinic acid (ALA) reduces arsenic toxicity stress in wheat (Triticum aestivum L.). Journal of Plant Growth Regulation, 42(6), 3303–3322.
Mohammadi S, Shafiee M, Faraji SN, Rezaeian M, Ghaffarian-Bahraman A. Contamination of breast milk with lead, mercury, arsenic, and cadmium in Iran: a systematic review and meta-analysis. Biometals: Int J role Metal ions Biology Biochem Med. 2022;35(4):711–28. https://doi.org/10.1007/s10534-022-00395-4.
Freire C, Iribarne-Durán LM, Gil F, Olmedo P, Serrano-Lopez L, Peña-Caballero M, Hurtado JA, Alvarado-González NE, Fernández MF, Peinado FM, Artacho-Cordón F, Olea N. Concentrations and determinants of lead, mercury, cadmium, and arsenic in pooled donor breast milk in Spain. Int J Hyg Environ Health. 2022;240:113914. https://doi.org/10.1016/j.ijheh.2021.113914.
Sharafi K, Nakhaee S, Azadi NA, Mansouri B, Miri Kermanshahi S, Paknahad M, Habibi Y. Human health risk assessment of potentially toxic elements in the breast milk consumed by infants in Western Iran. Sci Rep. 2023;13(1):6656. https://doi.org/10.1038/s41598-023-33919-0.
Bassil M, Daou F, Hassan H, Yamani O, Kharma JA, Attieh Z, Elaridi J. Lead, cadmium and arsenic in human milk and their socio-demographic and lifestyle determinants in Lebanon. Chemosphere. 2018;191:911–21. https://doi.org/10.1016/j.chemosphere.2017.10.111.
Lin X, Wu X, Li X, Zhang D, Zheng Q, Xu J, Lu S. Infant exposure to trace elements in breast milk, infant formulas and complementary foods from southern China. Sci Total Environ. 2022;838(Pt 4):156597. https://doi.org/10.1016/j.scitotenv.2022.156597.
Ghane ET, Khanverdiluo S, Mehri F. The concentration and health risk of potentially toxic elements (PTEs) in the breast milk of mothers: a systematic review and meta-analysis. J Trace Elem Med Biology: Organ Soc Minerals Trace Elem (GMS). 2022;73:126998. https://doi.org/10.1016/j.jtemb.2022.126998.
Çebi A, Şengül Ü. Toxic metal and trace element status in the breast milk of Turkish new-born mothers. J Trace Elem Med Biology: Organ Soc Minerals Trace Elem (GMS). 2022;74:127066. https://doi.org/10.1016/j.jtemb.2022.127066.
Sternowsky HJ, Moser B, Szadkowsky D. Arsenic in breast milk during the first 3 months of lactation. Int J Hyg Environ Health. 2002;205(5):405–9. https://doi.org/10.1078/1438-4639-00161.
Nakhaee S, Shadmani FK, Sharafi K, Kiani A, Azadi NA, Mansouri B, Karamimatin B, Farnia V. Evaluation of some toxic metals in breast milk samples with dietary and sociodemographic characteristics: a case study of Kermanshah, Western Iran. Environ Sci Pollut Res Int. 2023;30(2):4502–9. https://doi.org/10.1007/s11356-022-22495-x.
Kumar A, Rahman MS, Kumar R, Ali M, Niraj PK, Srivastava A, Singh SK, Ghosh AK. (2019b) Arsenic contamination in groundwater causing impaired memory and intelligence in school children of Simri village of Buxar district of Bihar. J Mental Health Hum Behav;24:132–8. https://doi.org/10.4103/jmhhb.jmhhb_31_18.
Samiee F, Vahidinia A, Taravati Javad M, Leili M. Exposure to heavy metals released to the environment through breastfeeding: a probabilistic risk estimation. Sci Total Environ. 2019;650(Pt 2):3075–83. https://doi.org/10.1016/j.scitotenv.2018.10.059.
Taravati Javad M, Vahidinia A, Samiee F, Elaridi J, Leili M, Faradmal J, Rahmani A. Analysis of aluminum, minerals and trace elements in the milk samples from lactating mothers in Hamadan, Iran. J Trace Elem Med Biology: Organ Soc Minerals Trace Elem (GMS). 2018;50:8–15. https://doi.org/10.1016/j.jtemb.2018.05.016.
Mohammadi Y, Dargahi A, Leili M, Samiee F. Worldwide arsenic levels in human breast milk and probabilistic health risk assessment: a systematic review and meta-analysis. Environ Health Eng Manage J. 2023;10(4):469–81.
Xia W, Hu J, Zhang B, Li Y, Wise JP, Sr, Bassig BA, Zhou A, Savitz DA, Xiong C, Zhao J, du X, Zhou Y, Pan X, Yang J, Wu C, Jiang M, Peng Y, Qian Z, Zheng T, Xu S. A case-control study of maternal exposure to chromium and infant low birth weight in China. Chemosphere. 2016;144:1484–9. https://doi.org/10.1016/j.chemosphere.2015.10.006.
Samanta G, Das D, Mandal BK, Chowdhury TR, Chakraborti D, Pal A, Ahamed S. Arsenic in the breast milk of lactating women in arsenic-affected areas of West Bengal, India and its effect on infants. J Environ Sci Health A. 2007;42(12):1815–25. https://doi.org/10.1080/10934520701566785.
Stone R. Food safety. Arsenic and paddy rice: a neglected cancer risk? Volume 321. Science (New York; 2008. pp. 184–5. 5886https://doi.org/10.1126/science.321.5886.184.
Saha GC, Ali MA. Dynamics of arsenic in agricultural soils irrigated with arsenic contaminated groundwater in Bangladesh. Sci Total Environ. 2007;379(2–3):180–9. https://doi.org/10.1016/j.scitotenv.2006.08.050.
Concha G, Vogler G, Nermell B, Vahter M. Low-level arsenic excretion in breast milk of native andean women exposed to high levels of arsenic in the drinking water. Int Arch Occup Environ Health. 1998;71(1):42–6. https://doi.org/10.1007/s004200050248.
Quansah R, Armah FA, Essumang DK, Luginaah I, Clarke E, Marfoh K, Cobbina SJ, Nketiah-Amponsah E, Namujju PB, Obiri S, Dzodzomenyo M. Association of arsenic with adverse pregnancy outcomes/infant mortality: a systematic review and meta-analysis. Environ Health Perspect. 2015;123(5):412–21. https://doi.org/10.1289/ehp.1307894.
Vahter M. Effects of arsenic on maternal and fetal health. Annu Rev Nutr. 2009;29:381–99. https://doi.org/10.1146/annurev-nutr-080508-141102.
U.S. EPA. Child-Specific Exposure Factors Handbook. (2008, Final Report). U.S. Environmental Protection Agency, Washington, DC, EPA/600/R-06/096F, 2008.
Narsimha A, Rajitha S. 2018. Spatial distribution and seasonal variation in fluoride enrichment in groundwater and its associated human health risk assessment in Telangana State, South India. 24:2119–32. https://doi.org/10.1080/10807039.2018.1438176
ICMR (Indian Council of Medical Research). Nutrient 566 requirements and recommended 567 dietary allowances for indians. Hyderabad: Indians National Institute of Nutrition; 2009. p. 334.
Acknowledgements
The authors are thankful to institute Mahavir Cancer Sansthan and Research Centre, Patna for providing necessary laboratorial and infrastructural facilities. Moreover, the authors are thankful to Indian Council of Medical Research, Government of India (ICMR F.No. 5/10/FR/79/2020-RBMCH, Dated. August 09, 2021) for the financial assistance of the entire research work and partially from DST-WTI project, Government of India (DST/TMD-EWO/WTI/2K19/ EWFH/2019/201).
Funding
The fund for this research work was provided by the grant from Indian Council of Medical Research (ICMR F.No. 5/10/FR/79/2020-RBMCH, Dated. 09/08/2021), Government of India.
Author information
Authors and Affiliations
Contributions
The entire experimental work was conceptualized by A.K and A.K.G. The field work sampling was carried out by R.A, K.K, N.K.C, S.A, A.K. In the manuscript writing A.K, R.A, K.K, D.K., A.B., S.S, S.K., A.S., M.S., and A.K.G., contributed the majority of writing activities, but support was also provided by M.A., T.P., K.S.V. Literature search was done by A.S., R.A, K.K., M.K., N.K.C., P.K.N., & S.A. Figures were developed by A.K., R.A., K.K., S.K. and A.B. The study design was carried out by A.K., and A.K.G. The experimentation was carried out by M.K., R.A, K.K., S.A, P.K.N., and data analysis by A.K., A.K.G., M.A., D.K., A.S., M.S., S.S. and A.B. The final manuscript writing was done by A.K., R.A, D.K., K.K, A.B., S.K., M.S., and A.K.G. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethical approval
The entire research work was approved from the Institutional Ethics Committee of the Indian Council of Medical Research Unit- Rajendra Memorial Research Institute of Medical Sciences (MoU for Ethics approval), Patna, Bihar, India, which granted the ethical clearance with IEC Letter No. RMRI/EC/24/2020 dated September 26, 2020. Before the investigation began, all patients were briefed about the study’s aims, and signed informed consent was obtained. The study was carried out in accordance with Indian Council of Medical Research, Government of India ethical guidelines for research involving human subjects and the ethical standards of the Declaration of Helsinki.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
About this article
Cite this article
Kumar, A., Agarwal, R., Kumar, K. et al. High arsenic contamination in the breast milk of mothers inhabiting the Gangetic plains of Bihar: a major health risk to infants. Environ Health 23, 77 (2024). https://doi.org/10.1186/s12940-024-01115-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12940-024-01115-w