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Association of same-day urinary phenol levels and cardiac electrical alterations: analysis of the Fernald Community Cohort

Environmental Health volume 23, Article number: 76 (2024) Cite this article

Abstract

Background

Exposure to phenols has been linked in animal models and human populations to cardiac function alterations and cardiovascular diseases, although their effects on cardiac electrical properties in humans remains to be established. This study aimed to identify changes in electrocardiographic (ECG) parameters associated with environmental phenol exposure in adults of a midwestern large cohort known as the Fernald Community Cohort (FCC).

Methods

During the day of the first comprehensive medical examination, urine samples were obtained, and electrocardiograms were recorded. Cross-sectional linear regression analyses were performed.

Results

Bisphenol A (BPA) and bisphenol F (BPF) were both associated with a longer PR interval, an indication of delayed atrial-to-ventricle conduction, in females (p < 0.05) but not males. BPA combined with BPF was associated with an increase QRS duration, an indication of delayed ventricular activation, in females (P < 0.05) but not males. Higher triclocarban (TCC) level was associated with longer QTc interval, an indication of delayed ventricular repolarization, in males (P < 0.01) but not females. Body mass index (BMI) was associated with a significant increase in PR and QTc intervals and ventricular rate in females and in ventricular rate in males. In females, the combined effect of being in the top tertile for both BPA urinary concentration and BMI was an estimate of a 10% increase in PR interval. No associations were found with the other phenols.

Conclusion

Higher exposure to some phenols was associated with alterations of cardiac electrical properties in a sex specific manner in the Fernald cohort. Our population-based findings correlate directly with clinically relevant parameters that are associated with known pathophysiologic cardiac conditions in humans.

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Background

Phenols are a group of synthetic chemicals that are extensively used in consumer goods and products [1,2,3]. For example, bisphenol A (BPA) and its analogs bisphenol F (BPF) and bisphenol S (BPS) are used in the manufacturing of a wide range of consumer plastics goods such as food containers, food cans, water bottles, baby bottles, dental sealants and water pipes, parabens are used as preservatives in cosmetics, pharmaceuticals, foods, and beverages, and triclosan (TCS) and triclocarban (TCC) are antibacterial chemicals used in personal care products such as detergents, soaps, lotions, toothpastes, and shampoos [1, 4,5,6]. In addition, 2.4-dichlorophenol (2,4-DCP) is used in synthesis of phenoxy acid herbicides. Due to their high production and extensive use, phenols are common environmental chemicals, and are present in surface and drinking water, soils, household dust, air, and sediments [1, 5, 6]. There is well-documented human exposure to environmental phenols. For example, in the earliest measures in urine from the National Health and Nutrition Exam Survey (NHANES, 2003–2004), BPA was detected in 92.6% of the population with a geometric mean urinary concentration of 2.64 ng/mL (years 2003-04), 2.4-DCP in 81.2% of the population with a geometric mean of 1.04 ng/mL (years 2003-04), and TCC in 74.6% of the population with a geometric mean of 13.0 ng/mL [7,8,9].

Phenols are also known environmental endocrine disruptors (EDCs), which interfere with the actions of native sex hormones and have a range of potentially adverse impacts on human health [1,2,3]. Several phenols have been shown to have cardiovascular toxicities. In particular, multiple epidemiological studies and independent analyses of NHANES have demonstrated that higher urinary BPA concentrations were associated with cardiovascular diagnoses, including coronary heart disease, angina, and peripheral arterial disease [10,11,12]. Experimental studies show that BPA exposure results in alteration of cardiac Ca2+ handing, arrhythmogenesis, cardiac remodeling, alteration of cardiac function, oxidative stress and altered autonomic regulation [13,14,15,16,17,18]. Many of these cardiac toxicities of BPA in experimental studies are shared by its analogs, including BPS and BPF [4, 16, 19, 20]. In addition, TCC has been shown to result in cytotoxicity and arrhythmic beating in human inducible pluripotent stem cell derived cardiomyocytes (hiPSC-CMs) [21], and TCS has been shown to impair cardiac excitation-contraction coupling and cardiomyocyte differentiation [22, 23].

A notable gap in the current knowledge on the cardiac toxicity of phenols is the lack of understanding of the impact of these chemicals on the cardiac electrical properties in humans. Electrical excitation and conduction are fundamental to normal cardiac physiology [24]. Cardiac electrical abnormalities play a key role in cardiac diseases and are a major contributor to human morbidity and mortality [25,26,27]. Experimental evidence shows that BPA and its analogs can impact several cardiac ion channels including the L-type and T-type Ca2+ channels, the rapid delay rectifier K+ channel and ryanodine receptors, as well as affecting electrophysiological properties in hiPSC-CMs, canine ventricular myocytes, and rodent cardiac myocytes [15, 16, 19, 28,29,30]. Such bisphenol-induced electrical alterations can result in the development of arrhythmias under certain pathophysiological conditions in hiPSC-CMs and rodent hearts [16, 18, 31]. These findings point to the need to define the impact of environmental phenols on the cardiac electrical properties of human hearts.

In the present cross-sectional study, we aimed to identify changes in electrocardiographic (ECG) parameters in a midwestern large population, known as the Fernald Community Cohort (FCC). We characterized urinary phenol concentrations in members of the FCC and examined the association of phenol exposure and alterations of cardiac electrical properties, using key ECG parameters from examinations done on the same day as the urine collection.

The FCC consists of nearly ten thousand individuals who participated in medical monitoring because they had lived for at least three years within five miles of a uranium processing plant. The facility’s primary mission was to produce high-purity uranium metal necessary for nuclear weapons production. A uranium exposure algorithm was developed by the Centers for Disease Control and Prevention (CDC) as part of the Fernald Dosimetry Reconstruction project [32]. A significant proportion of those in the screening program received airborne environmental uranium exposure that was negligible compared to background exposure [33] and were categorized into the lowest exposure group, with exposure ≤ 0.2 µg/m3-yr beyond background. Only those in this lowest exposure category were eligible for the present study. The FCC cohort, with its ECG data and concurrently collected biosamples at the time of the first examination, offered an invaluable dataset for examining the potential cardiac electrical impact of phenols in humans. This study addressed the hypothesis that in humans, higher exposure level to at least some environmental phenols is associated with changes in ECG markers of cardiac function and risk of arrhythmia. The key ECG markers used in this study included QT interval, PR interval, QRS duration and RR interval (or heart rate). QT interval represents the duration of ventricular excitation of the electric cardiac cycle. PR interval represents atrium-to-ventricle conduction through the atrioventricular (AV) node which is modulated by both the AV node conduction properties as well as vagal tone and aging. QRS duration represents ventricular depolarization. Lastly, RR interval represents the time elapsed between two successive ventricular beats and is the reciprocal of heart rate.

Methods

Urine sample storage, subject selection and ECG analysis

Fernald Cohort urine samples and ECG data were collected at the first examination in 1991–1994. Urine samples were aliquoted and immediately stored, without buffer, in 1.0 ml polypropylene tubes at -80 °C. Members of the Fernald cohort eligible for the present study were from the portion of the cohort with negligible uranium exposure, were 18–80 years of age at the time of the first examination. Those with conditions that are common causes of induced changes in ECG P wave, QTS complex, QT interval or heart rate were excluded. These excluded conditions/diagnoses are based on the participants’ medical record and include cardiomyopathy, the long QT syndrome, prior cardiac arrest, cardiac conduction abnormalities including left bundle branch hemiblock, left or right bundle branch block, or bilateral bundle branch block, taking beta-blockers or antiarrhythmic drugs. Those with arrhythmia (e.g., atrial/ventricular tachycardia, flutter or fibrillation) that resulted in uninterpretable ECG P wave, QTS, QT interval or heart rate values were also ineligible. Of the remaining members of the cohort, 302 males and 302 females were randomly selected. The mean age was 39 ± 13 years. The vast majority self-identified as white with a broad representation of socio-economic and educational backgrounds (Tables 1 to 3). All had interpretable ECG values.

Table 1 Electrocardiograph and other basic medical information for the Fernald Community Cohort
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ECGs were read by physicians who were board certified in cardiology. Four key ECG parameters, corrected QT interval, PR interval, duration of the QRS complex, and RR interval were included in this analysis. QT interval was corrected for heart rate (calculated as QTc = QT/√RR). Descriptive statistics were used to identify possible outlying observations, and the tenability of parametric assumptions were assessed prior to estimating the models to evaluate our primary hypotheses.

Measurement of urine phenol concentrations

Twelve phenol analytes were analyzed in the urine (ng/mL) of 604 participants. The Centers for Disease Prevention and Control (CDC) Division of Laboratory Sciences conducted the analysis using an automated on-line column switching HPLC-MS/MS method with peak focusing. If the percentage of detection in the population was less than 40% then analysis was not performed on the analyte [8]. Phenols analyzed for this study included BPA, benzophenone-3 (BP-3), bisphenol-F (BPF), 2,4, dichlorophenol (24-DCP), 2,5 dichlorophenol (25-DCP), methyl paraben (M-PB), propyl paraben (P-PB), triclocarban (TCC), and triclosan (TCS).

Statistical analysis

Median and mean statistics for the outcomes and risk factors were calculated for both the entire cohort and stratified by sex. The sex specific statistics were tested for significance using Fisher’s exact test for the association of the phenol urinary biomarker level with sex for categorical variables and a linear model was used to test the association with sex for continuous variables. P values were provided based on F test in the Type III Sum of Squares output. To determine the association between the urinary concentrations of phenols and alteration of ECG parameters, creatinine-corrected urine phenol concentrations (BPA, DCP24, DCP25, BPF, BP3, MPB, PPB, TCS, TCC, combination of BPA and BPF, combination of DCP24 and DCP25) were log-transformed or categorized into tertiles for analyses. Multivariate linear regression analyses were performed, where the ECG parameter in miliseconds (ms) was dependent variable and creatinine-corrected environmental chemical was independent variable. Because of the sex differences in ECG parameters and since phenols are known endocrine disruptors, sex-specific analyses were conducted in order to fully characterize the effect of creatinine-corrected environmental phenols on ECG parameters for each gender separately. Different ECG parameters had different sets of covariates but all included sex, age at exam, smoking pack-year history exam, alcohol consumption at enrollment, and physician(s) reading the ECG (to account for possible physician-specific variations in ECG interpretation), using the F test in the Type III Sum of Squares output. Other parameters such as serum cholesterol (mg/dL) and triglyceride (mg/dL) were included after a review of the literature and retained as covariates in all final analyses because of their statistical significance except for the effect on QRS duration. Serum potassium concentration was included in the analysis of QTc as reported in the literature [34]. The use of oral contraceptives or hormone replacement therapy (yes/no) were included in analyses of QTc and ventricular rate in the female subcohort.

Results

As shown in Table 1, the median and mean values for the ECG parameters of the participants were within normal limits. There was moderate use of alcohol and smoking among this cohort. The measured serum triglycerides and cholesterol values are presented and are within physiological range.

There were notable differences in the ECG parameters between male and female subjects at baseline (Table 2). Specifically, PR interval and QRS duration were all significantly longer in males, while QTc was significantly longer and heart rate significantly faster in females. There was no significant sex difference in age, BMI or smoking though females had significantly lower triglyceride, cholesterol and serum K+ levels. Demographic information is presented by sex in Table 3 showing a broad socio-economic distribution without significant differences between males and females. The participants are predominantly white which reflects the typical racial and ethnic composition of these rural Southwestern Ohio communities.

Urinary concentrations of the measured phenols stratified by sex are shown in Table 4. The cohort was widely exposed to the tested phenols with the exception of BPS, a newer BPA substitute. BPA, measured as total urinary level (free plus conjugated), was detected in 99.3% of the cohort with a mean concentration of 2.3 and 2.4 ng/mL (95% CI 2.1 to 2.6, and 2.2 to 2.5), in females and males, respectively. These BPA exposure levels in urines collected in 1990 to 1993 are similar to later reported values in the US populations [8, 35, 36]. Key differences between the sexes include significantly higher levels of BP3, M-PB and P-PB in females, and higher levels of DCP24, TCC and TCS in males. Levels of DCP25, BPA, BPF and BPS were similar between males and females.

Table 2 Electrocardiograph and other basic medical information for the Fernald Community Cohort stratified by sex
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Table 3 Demographic information
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Table 4 Urinary phenol measurements in the Fenald Community Cohort stratified by sex
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The sex specific associations between BPA exposure and covariates and the measured ECG parameters are shown in Table 5. In females but not males, higher urinary BPA was associated with longer PR interval (4.01 ms increase in PR interval per unit increase in ln[BPA]; P < 0.05). In addition, higher BMI in females was associated with longer QTc (0.40 ms per unit BMI; P < 0.05), longer PR interval (0.59 ms per unit BMI; P < 0.01), and longer RR interval (i.e., slower heart rate; 0.36 ms in RR per unit BMI; P < 0.01). In males, BMI was only associated with longer RR interval (0.49 ms per unit BMI; P < 0.01). In females, age was associated with a small reduction of QRS (0.09 ms per year; P < 0.05), and in males, age was associated with longer QTC (0.26 ms per year; P < 0.01) and PR interval (0.51 ms per year; P < 0.001).

Table 5 Effect of BPA exposure on ECG parameters
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Further, as noted above, sex was a strong covariate; the female sex was associated with longer QTc (7.28 ± 1.73 ms; P < 0.0001), shorter PR interval (8.44 ± 1.92 ms; P < 0.0001), shorter QRS (8.94 ± 0.89 ms; P < 0.0001), and higher RR interval (4.63 ± 1.11 ms; P < 0.0001).

The associations between other phenols and changes in ECG parameters are found in Table 6. Similar to BPA, higher urinary BPF and BPA plus BPF were associated with longer PR interval in the female population (3.4 and 5.09 ms increase in PR interval per unit increase in ln[BPF] and ln[BPA + BPF], respectively; P < 0.01). In females, higher BPA plus BPF was associated with longer QRS duration (1.5 ms increase in QRS per unit increase in ln[BPA + BPF]; P < 0.05). In males, TCC exposure was associated with prolongation of QTc (1.38 ms per unit of ln[TCC]; P < 0.01). When females and males were analyzed as a single cohort there were only significant associations noted between QTc and TCC and PR interval and BPA + BPF (Suppl Table 1). No significant associations were noted between any phenol and RR interval.

Table 6 Effect of phenol exposure on ECG parameters
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The association between phenols and ECG parameters is summarized in Fig. 1. The strong sex dichotomy is evident. The female cohort showed significant increases in PR interval associated with BPA, BPF, and BPA + BPF exposure, while BPA + BPF exposure was also associated with increased QRS duration. The male cohort demonstrated an association between TCC levels and QTC, but no other associations were noted.

Fig. 1
figure 1

Graphic summary of the effect of phenol exposure on ECG parameters in the Fernald Cohort. Effect size represents the change in the value of ECG parameters with a change in one unit of log transformed urinary phenol concentration. Red bars illustrate effects that have statistical significance. *: P < 0.05; **: P < 0.01

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While higher phenol exposure was only associated with small changes in ECG parameters, such change may be more pronounced in certain BMI or age subpopulation groups. Higher BPA was associated with PR interval prolongation in females (see Table 5; Fig. 1). Dividing both urinary BPA and BMI into tertiles revealed such association was particularly pronounced in females in the top BMI tertile group (Fig. 2, top). In females, the combined effect of being in the top tertile for both BPA urinary concentration and BMI was an estimate of 14.8 ms, or about 10% increase in PR interval (Fig. 2, top). Similarly, ECG metrics can vary significantly by age and BPA exposure may have a particular effect on ECG in certain age groups. Dividing the cohort into tertiles based on age and urinary BPA suggests that BPA may have an association with QT prolongation in the older age group. Particularly in males, QTc interval increased with BPA exposure in the older age group but not in the mid to lower age groups (Fig. 2, bottom).

Fig. 2
figure 2

Top: Relationship between PR interval, urinary BPA concentration, and BMI, with both urinary BPA and BMI divided into tertiles. BPA categories: 1, < 1.65; 2, 1.65–2.96; 3, > 2.96 (ng/mL); BMI categories: 1, < 24.2; 2, 24.2–28.4; 3, > 28.4. Bottom: Relationship between QTc, urinary BPA concentration, and age, with both urinary BPA and age divided into tertiles. BPA categories: 1, < 1.65; 2, 1.65–2.96; 3, > 2.96 (ng/mL); age categories: 1, 18–31; 2, 32–45; 3, 46–77 (years old)

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Discussion

Extensive experimental and epidemiological evidence points to the cardiac toxicity of bisphenol-type environmental chemicals. However, the impact of bisphenols and other phenols on the cardiac electrical properties in humans is entirely unknown. This is the first study to examine the associate of phenol exposure and ECG alterations in a human cohort, and provides insights into phenol associated, sex-specific changes in cardiac electrical properties. The key findings of this study relate to the changes observed in ECG parameters, PR interval and QTc in particular, as it pertains to BPA and other phenol levels when analyzed by sex. These alterations of cardiac electrical properties have clear physiological and pathological implications.

PR interval represents the electrical conduction between the atria and the ventricle, and prolongation of the interval is associated with increasing age as the AV node function decreases [37, 38]. This is relevant as advanced AV blocks are a common indication for placement of artificial cardiac pacemakers [39] and are also relevant in an aging population that is prone to develop atrial arrhythmias (such as atrial fibrillation) that depend on normal AV conduction to maintain cardiac output [40,41,42]. In this study we found the PR interval increases with age in both males and females as expected, and increases in females in association with BPA and BPF exposure. Further, the combined effect of BPA exposure with elevated BMI was associated with an approximate 10% increase in PR interval in females. This association between PR prolongation and bisphenol exposure is generally consistent with published experimental data showing that exposure to BPA delayed AV conduction and increased the PR interval in excised female rat hearts [43]. Conduction velocity in cardiac tissue is determined by the size of the action potential-generating inward current [44]. It is possible that BPA reduces AV node conduction through inhibition of the L-type Ca2+ current, which is the dominant inward current in AV node myocytes and a key determinant of AV node conduction velocity [44, 45]. Recently, we have shown that 1 nM BPA acutely inhibited the L-type Ca2+ current in hiPSC-CMs, including in nodal-like myocytes [16], and that long term exposure to 1 nM BPA inhibited the L-type Ca current in hiPSC-CMs through reduction of the L-type Ca2+ channel protein expression level [19]. Similarly, low-doses of BPA inhibited the L-type Ca2+ current in female rat cardiomyocytes in a dose-dependent manner [14]. At higher, µM doses, BPA has also been shown to suppress the L-type current/channel in hiPSC-CMs and heterologously expressed in HEK cells [29, 30]. Such BPA-mediated inhibition of the L-type Ca2+ channel may provide a cellular mechanism for the observed prolongation of the PR interval in the Fernald Cohort.

It has been well-established that prolongation of the QT interval is a key arrhythmogenic mechanism and are associated with adverse cardiac outcomes, specifically sudden cardiac death [25,26,27]. QT prolongation is an indication of delay in ventricular repolarization, which can lead to ectopic ventricular excitation and malignant ventricular arrhythmias [25, 26, 46]. QT prolongation is often caused by genetic mutations in cardiac ion channels, predominantly K+ and Na+ channels, and the resulting prolongation of ventricular action potential [47, 48]. QT prolongation can also be produced by adverse blockade of cardiac ion channels by drugs or environmental chemicals, and is one of the central issues in cardiac safety and cardiotoxicity assessment [49,50,51,52,53]. Examples of QT prolongation-related cardiac toxicity of environmental chemicals include trivalent arsenic As3+ and organophosphate poisoning [54,55,56,57]. Here, we show that higher urine level of TCC was associated with longer QTc in males but not females. TCC, an antibacterial chemical once common in personal care products, is now banned for usage in the US. Information on the association between TCC exposure and QT prolongation toxicity may help retrospective understanding of the health outcomes of the Fernald Cohort. In addition, even though there is no association between BPA exposure and QT change at the cohort level, we found that in older males (top tertile), higher BPA exposure may have an association with QTc prolongation, as shown in Fig. 2. While QTc difference between the lowest to the highest groups was modest (about 20 msec), from a population perspective even smaller increases in QTc have been shown to be associated with increased risk of adverse outcomes. For instance, Zhang and colleagues found that any increase in QT interval was associated with a small but measurable change in total and cardiovascular mortality and specifically sudden cardiac death [58]. Our findings have important implications for the QT prolongation cardiotoxicity of BPA, and likely other related bisphenol-type chemicals, in older males.

From a cellular physiologic perspective, BPA has been shown to inhibit the IKr K current, which plays a key role in cardiac repolarization. We showed in our previous studies that acute exposure to environmentally relevant low dose BPA (1 nM) inhibited the IKr current in hiPSC-CMs and canine ventricular myocytes. Such IKr inhibition resulted in delay in action potential repolarization in hiPSC-CMs and canine ventricular myocytes, and the net effect of inhibitions of IKr and the L-type current results in prolongation of QT interval [15, 16]. The pro-arrhythmic toxicity of such BPA-induced repolarization delay was illustrated by the marked increase in arrhythmic events under BPA exposure combined with pathophysiological conditions [16]. In addition, acute exposure to high doses (mid to high µM) BPA has also been shown to inhibit IKr in hiPSC-CMs and hERG (the molecular correlate of human IKr current) expressed in HEK 293 [30]. While these acute experimental exposure findings cannot be directly extrapolated to the exposure scenario in humans, they nevertheless offer a plausible cellular mechanism of the observed QT prolongation associated with BPA exposure in the top tertile age group.

No change in QRS duration or heart rate was found to be associated with exposure to any single tested phenol, while higher urine BPA plus BPF level was associated with slight QTS prolongation in females. QRS duration represents depolarization of the ventricles and is prolonged under disease conditions including heart failure, prior infarction, and/or development of a bundle branch block. The etiology of the QRS prolongation associated with BPA plus BPF levels is unknown, and further experimental and human population studies are needed to fully clarify this. That being noted, Hnatkova and colleagues found that, in healthy individuals, QRS duration is slightly longer in males in comparison with females (103.2 msec vs. 98.7 msec) [59], which is similar to the small differences we observed in this study.

The lack of effect of phenols on heart rate in the Fernald participants contrasts with previously reported acute stimulatory effect of low dose bisphenols on ex vivo rodent heart rate and pacing rate of nodal hiPSC-CMs [16, 31], and likely reflects the difference between chronic and acute phenol exposures. Exposure dose also appears to determine the impact of bisphenols on pacing rate; while nM low dose increases pacing rate, bisphenols have been shown to inhibit cardiac pacing at higher, µM dose [29, 30]. Further, the human heart rate is controlled by cardiac factors (such as sinus node automaticity) as well as extracardiac factors such as vagal tone, adrenaline secretion and sympathetic activity. The autonomic control of the heart rate in vivo may be another reason for the contrasting cohort vs. experimental findings on this parameter.

The similar effect of BPA and BPF we found in the Fernald Cohort is consistent with the generally similar cardiac toxicity reported for BPA and its analogs in experimental studies, including in hiPSC-based human cardiac models. (It is also worth noting the widespread exposure to BPF in the Fernald Cohort in the early 90’s, much before BPA-free products and BPA replacements became popular.) It has been shown that acute exposure to BPA, BPF, and other BPA analogs suppressed spike amplitude, beat period, field potential duration, and contractility in hiPSC-CMs, mostly at µM-range high doses [60]. Similarly, micromolar doses of BPA and BPF decreased the depolarization spike amplitude, and shortened the field potential, action potential duration, and calcium transient duration in hiPSC-CMs [61]. We showed that in human cardiac organoids, acute exposure to low dose (1 nM) BPA delayed cardiac repolarization and promoted the development of ectopic excitations and the toxicity was shared by its analogs including BPS, BPF and BPAF [16]. An exception to the generally similar cardiac effects of BPA and BPF is our recent finding that long term exposure to low dose BPA and BPAF, but not BPF, suppressed contractility and promoted hypertrophy in hiPSC-CMs and human cardiac organoids [19]. We show here that the female-specific effect of BPA and BPF on PR interval and QRS complex are similar, and our result (Fig. 2) is consistent with BPA and BPF having an apparent additive effect, suggesting that the bisphenol mixture effect should be further examined in humans.

We show here that higher exposure to some phenols was associated with alternations of ECG properties in the Fernald Cohort. Individual persons may experience more or less of an effect of BPA exposure on the ECG properties due to individual differences in absorption and metabolism of BPA. Regardless, it should be noted that these ECG changes at the population level are moderate and generally within the normal ECG parameter ranges. While these changes alone are unlikely to result in clinically significant cardiac electrical disease in healthy individuals, we believe that higher phenol exposure is a risk factor that can contribute to cardiac electrical abnormalities, particularly in subpopulations with existing pathophysiological conditions and predisposition. One such scenario is the combined effect of bisphenol-associated PR interval prolongation and BMI in females. As shown in Fig. 2, high exposure combined with high BMI can lead to sizable PR alteration in females. It is also possible that bisphenol-associated PR prolongation, particularly in high exposure individuals, can exacerbate existing AV block in patients with heart conduction disorders. Also, as noted above, age-based analysis reveals the possible QT prolongation toxicity of BPA in the older male subpopulation. Such a subpopulation-based toxicity assessment approach can better identify cardiac toxicities of environmental chemicals that would otherwise be difficult to identify in the general population.

The cross-sectional nature of the study allows us to determine association but not causality. Further, the temporal variability of BPA, and likely other phenols, is well known [62,63,64,65], and a one-time measurement of phenol levels does not represent lifetime exposure. In addition, the analyzed samples were collected from the Fernald population in the early 90’s (1991–1994) before the ramp up of BPA-alternatives (such as BPS) which would shift the exposure levels compared to present day. However, even with these limitations, the FCC is highly valuable because it is unusual to have a large population-based cohort with simultaneous urine specimen collection and ECG recordings, which allowed us to determine the association of real-time (not lifetime) phenol exposure with ECG markers.

In conclusion, our population-based study shows, for the first time, that higher urinary levels of environmental phenols, including BPA, BPF, and TCC, were associated with sex-specific alterations in cardiac electrical-conduction properties in the Fernald Cohort. Our findings correlate with clinically relevant parameters that are associated with known pathologic conditions in humans. Our findings may have implication for the cardiac toxicity of these chemicals, particularly in predisposed subpopulations.

Data availability

Data is provided within the manuscript or supplementary information files.

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Funding

This work was supported by the National Institute of Environmental Health Sciences (NIEHS) grants ES027855 (HSW) and ES028527 (SMP), and the University of Cincinnati Center for Environmental Genetics through the NIEHS award P30ES006096.

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Authors and Affiliations

  1. Division of Cardiovascular Health and Disease, Department of Internal Medicine, College of Medicine, University of Cincinnati, Cincinnati, OH, USA

    Jack Rubinstein

  2. Department of Environmental and Public Health Sciences, College of Medicine, University of Cincinnati, Cincinnati, OH, USA

    Susan M. Pinney & Changchun Xie

  3. Department of Pharmacology, Physiology and Neurobiology, College of Medicine, University of Cincinnati, Cincinnati, OH, USA

    Hong-Sheng Wang

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JR: conception of the work, analysis, interpretation of data, drafted the work; SMP: conception and design of the work, analysis, interpretation of data, substantively revised work; CX: design of the work, analysis, interpretation of data; HSW: conception and design of the work, interpretation of data, drafted the work. All authors have approved the submitted version (and any substantially modified version that involves the author’s contribution to the study); and have agreed both to be personally accountable for the author’s own contributions and to ensure that questions related to the accuracy or integrity of any part of the work, even ones in which the author was not personally involved, are appropriately investigated, resolved, and the resolution documented in the literature.

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Correspondence to Hong-Sheng Wang.

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Rubinstein, J., Pinney, S.M., Xie, C. et al. Association of same-day urinary phenol levels and cardiac electrical alterations: analysis of the Fernald Community Cohort. Environ Health 23, 76 (2024). https://doi.org/10.1186/s12940-024-01114-x

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Keywords

Environmental Health

ISSN: 1476-069X