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PM2.5 metal exposures and nocturnal heart rate variability: a panel study of boilermaker construction workers
© Cavallari et al; licensee BioMed Central Ltd. 2008
- Received: 07 January 2008
- Accepted: 09 July 2008
- Published: 09 July 2008
To better understand the mechanism(s) of particulate matter (PM) associated cardiovascular effects, research priorities include identifying the responsible PM characteristics. Evidence suggests that metals play a role in the cardiotoxicity of fine PM (PM2.5) and in exposure-related decreases in heart rate variability (HRV). We examined the association between daytime exposure to the metal content of PM2.5 and night HRV in a panel study of boilermaker construction workers exposed to metal-rich welding fumes.
Twenty-six male workers were monitored by ambulatory electrocardiogram (ECG) on a workday while exposed to welding fume and a non-workday (baseline). From the ECG, rMSSD (square root of the mean squared differences of successive intervals) was summarized over the night (0:00–7:00). Workday, gravimetric PM2.5 samples were analyzed by x-ray fluorescence to determine metal content. We used linear mixed effects models to assess the associations between night rMSSD and PM2.5 metal exposures both with and without adjustment for total PM2.5. Matched ECG measurements from the non-workday were used to control for individual cardiac risk factors and models were also adjusted for smoking status. To address collinearity between PM2.5 and metal content, we used a two-step approach that treated the residuals from linear regression models of each metal on PM2.5 as surrogates for the differential effects of metal exposures in models for night rMSSD.
The median PM2.5 exposure was 650 μg/m3; median metal exposures for iron, manganese, aluminum, copper, zinc, chromium, lead, and nickel ranged from 226 μg/m3 to non-detectable. We found inverse linear associations in exposure-response models with increased metal exposures associated with decreased night rMSSD. A statistically significant association for manganese was observed, with a decline of 0.130 msec (95% CI: -0.162, -0.098) in night rMSSD for every 1 μg/m3 increase in manganese. However, even after adjusting for individual metals, increases in total PM2.5 exposures were associated with declines in night rMSSD.
These results support the cardiotoxicity of PM2.5 metal exposures, specifically manganese. However the metal component alone did not account for the observed declines in night HRV. Therefore, results suggest the importance of other PM elemental components.
- Heart Rate Variability
- Metal Exposure
- Night Period
- Welding Fume
- Silica Exposure
The consistent association between particulate matter (PM) exposures and cardiovascular health effects is well documented [1–3]. As we seek to better understand the mechanisms, research priorities include identifying the PM characteristic(s) responsible for the observed cardiovascular health effects [1, 4, 5]. Evidence from epidemiological and toxicological studies suggest that composition may play a role in particle-associated cardiovascular responses [4, 5].
To date, the majority of epidemiological studies have characterized PM exposures by mass concentration. PM with an aerodynamic diameter ≤ 2.5 μm (PM2.5) is often measured due to its ability to penetrate deep into the alveolar regions of the lung, where it can initiate cardiovascular and other health effects. Some studies have focused on identifying air pollution sources responsible for the observed health effects, and there is growing evidence linking traffic-related particle exposures to cardiovascular responses . However, information is lacking on the specific chemical or class of chemical components associated with adverse cardiovascular health outcomes [5, 7]. Through source-related studies and toxicological evidence, particulate matter components including soluble organic compounds and metals, specifically transition metals, have been linked to cardiovascular outcomes . The role of metals is further implicated by a study of air pollution exposures among older men finding that metal processing genes modified cardiovascular autonomic responses to PM2.5.
Our previous research among a cohort of boilermaker construction workers or "boilermakers" occupationally exposed to high-levels of metal-rich PM is the only epidemiological study  that has examined the association between specific particulate matter metal components and cardiovascular outcomes in humans. We examined the association between workday heart rate variability (HRV), a measure of cardiovascular autonomic control, and workday PM2.5 metal exposures and found statistically significant increases in the 5-min SDNN (standard deviation of normal-to-normal intervals), averaged over the 8–10 hour workday with personal lead and vanadium exposures . This is contrary to the majority of studies reporting an inverse association between HRV and total PM2.5 exposure .
Our previous investigation which monitored daytime HRV may not have captured the relevant time-period of response. In a subsequent investigation within this cohort, we observed that as compared to the day, night may be a the more relevant time period to capture workday particle-related changes in cardiovascular autonomic response . We observed an inverse exposure-response relationship between workday PM2.5 mass and long-duration night HRV, specifically rMSSD (square root of the mean squared differences of successive intervals) and no associations between day HRV and workday PM2.5 mass concentration. However, it remains unclear what role the metal composition plays in the particle-related nocturnal HRV changes that we observed. In the current study we sought to examine the association between the metal components of PM2.5 both independently and after adjustment for total PM2.5 and rMSSD during the night period in a panel study of boilermakers.
The Institutional Review Board at the Harvard School of Public Health approved the study protocol, and informed written consent was obtained from each adult prior to participation. From 1999 to 2006, we recruited 36 boilermakers at an apprentice welding school to participate in extensive ambulatory electrocardiogram (ECG) monitoring over two 24-hour periods on both a workday and a non-workday. In 2004 through 2006, in addition to ECG monitoring, 26 boilermaker welders were monitored for workday PM2.5exposures which were then analyzed by x-ray fluorescence (XRF) for elemental content. These boilermakers were invited to participate in the study on multiple occasions over the two-year sampling period; 22 (85%) were monitored on one occasion, 3 (12%) were monitored twice, and one was monitored on three occasions for a total of 31 monitoring occasions. On each monitoring occasion, boilermakers were continuously monitored over both a work and non-work day.
Workday monitoring took place at a union welding school, where boilermakers practiced welding, cutting, and grinding techniques. Boilermakers primarily performed shielded metal arc (stick) and gas metal arc welding (TIG), using base metals of mild steel (manganese alloys) and stainless steel (manganese, chromium, and nickel alloys) with electrodes composed mainly of iron with variable amounts of manganese (1–5%). Plasma arc or acetylene torch cutting and grinding also occurred. In addition to workday monitoring, participants were also continuously monitored over a non-workday when they were not welding, grinding or cutting, to establish baseline night HRV. This occurred within 6 months of workday monitoring, but 81% of the observations occurred within the same week. A questionnaire was used to collect information on medical history, current cardiopulmonary symptoms, medication use, demographics, occupational history, and lifestyle factors including smoking history.
ECG monitoring and tape processing
Participants were fitted with a standard 5-lead ECG Holter monitor. To facilitate good lead contacts, the participant's skin was shaved, if necessary, cleansed with an alcohol wipe, and slightly abraded. Study staff checked leads at the workplace periodically. Each tape was sent to Raytel Cardiac Services (Haddonfield, NJ) for processing and analysis using a DelMar Avionic (Irvine, CA) Model Strata Scan 563. Only beats with an RR interval between 0.6 and 1.5 sec and an RR ratio of 0.8–1.2 were included in the analysis. Trained technicians, blinded to the work and non-work periods, used standard criteria to accept or reject all normal or abnormal findings. Tapes were analyzed in the time domain, and indexes including the square root of the mean of the sum of the squared differences between adjacent NN intervals (rMSSD), the standard deviation of all NN intervals over the entire period (SDNN), and the mean of the standard deviations of all NN intervals for all 5-min segments (SDNNi) were calculated over the 7-hr night period (00:00 to 07:00). The current analysis is restricted to the rMSSD measure, which based on our previous analysis, best captures cardiovascular autonomic changes following PM2.5 exposure .
Particulate matter exposure assessment and analysis
Personal, integrated, gravimetric samples were collected over the duration of the work shift using a KTL cyclone (GK2.05SH, BGI Incorporated, Waltham, MA) with an aerodynamic diameter cutpoint of 2.5 μm used in line with a pump drawing 3.5 L/min of air. The cyclone was secured to the participant's shoulder in the breathing zone area, and the pump was placed in a padded pouch that was carried by the participant for the entire workday. Each cyclone was fitted with a cassette holding a 37 mm polytetrafluoroethylene membrane filter (Gelman Laboratories, Ann Arbor, MI). The filters were weighed in a temperature- and humidity-controlled room using a standard protocol before and after sampling on an MT5 micro-balance from Mettler-Toledo Incorporated (Columbus, OH). We divided the blank corrected mass of each sample by the sample air volume to calculate the PM2.5 mass concentration.
The filters from the cyclone samples were analyzed for elemental components using XRF. Desert Research Institute (Reno, NV, USA) performed all XRF analyses on the PANanalytical Epsilon 5 Energy Dispersive XRF analyzer (Almelo, the Netherlands) and utilized standard operating procedures including quality control and assurance measures [11, 12]. For each element the corresponding limit of detection (LOD) was reported as μg of element per filter. Samples below the LOD were assigned the value of the LOD. Metal exposures were calculated by dividing the metal mass by the sampled air volume.
Paired t-tests were used to compare the mean rMSSD between work and non-work periods. Due to the skewed exposure distributions, exposure medians and interquartile ranges (Q25 – Q75) were calculated for total PM2.5 as well as the following metals: aluminum, chromium, copper, iron, lead, manganese, nickel, and zinc. Spearman correlations between PM mass and metal exposures were estimated.
To investigate the association between PM2.5 metal exposures and night HRV, we used linear mixed-effects regression models with random intercept for each subject and unstructured covariance. The mixed-effects models allowed us to account for the correlated outcomes among workers who participated on multiple occasions and to control for unmeasured covariates that differ across subjects. Regression models included a continuous covariate for non-work, night rMSSD to control for participant specific risk factors for HRV such as age and health status that don't vary over the time frame of interest. In addition, we adjusted all models for cigarette smoking by including a dichotomous variable representing smoking status at the time of monitoring. Each metal was modeled separately and due to small sample size, multiple metal models were not considered simultaneously. Since metal and total PM mass exposures covaried, we also investigated the effect of each metal, independent of PM2.5, by including total PM2.5 in the model along with the metals.
As an alternative approach designed to address the collinearity among exposure variables, we also investigated the association between night HRV and PM2.5 metal exposures using a two-step residual model. In the first step, each metal was regressed on total PM2.5 in a separate linear model, and the residuals were computed for each observation. Residuals are, by definition, the portion of the outcome (metal content) that is uncorrelated with the independent variable, total PM2.5 concentration. We therefore considered the residuals to be measures of the independent contribution of each metal and in the second step, treated them as new exposure variables in the regression models for the health outcome. The residual method approach was adapted from energy adjustment techniques used within nutritional epidemiology . All analyses were performed using SAS version 9.1.
Study population characteristics for boilermaker participants (n = 26)
Mean ± SD
or n (%)
43 ± 11
29 – 64
Nightb rMSSD (msec)
30.3 ± 16.0
32.0 ± 16.0
Composition and characteristics for personal, workday PM2.5 measurements (n = 31)
Q25 – Q75
337.0 – 1052.2
2.67 – 6.28
0.08 – 0.24
0.79 – 4.67
132.2 – 453.0
10.23 – 38.62
0.003 – 0.15
0.08 – 0.22
0.37 – 4.50
Spearman correlation coefficients within and between PM2.5 metal exposures and total PM2.5 exposure
Associations between night rMSSD and individual PM2.5 metal exposures
Associations between night rMSSD and residual metal exposures
Q25 – Q75
-0.57 – 0.59
-0.03 – 0.02
-1.30 – 0.95
(-0.010, – 0.000)
-41.89 – 34.08
-6.69 – 7.55
-0.07 – 0.05
-0.05 – 0.02
-1.69 – 1.24
Since the metal residual was no longer correlated with PM2.5, we controlled for PM2.5 mass and can interpret these results as the effect of increasing metal exposures while holding PM2.5 constant. After accounting for PM2.5 exposure, the associations between the individual metals and HRV weakened or changed in direction (Table 5, Model 4). However an inverse, linear exposure-response relationship remained for aluminum, manganese, and lead, as is consistent with Model 1, although the confidence intervals of these associations widened. In the residual model, holding each metal exposure constant, we observed consistent declines in HRV with increasing total PM2.5 exposure, with the exception of manganese, the associations were statistically significant (Table 5, Model 4).
This study provides valuable information on how the metal content of PM contributes to cardiovascular responses, specifically to changes in cardiovascular autonomic control. Our previous investigation found that PM2.5 mass was associated with night HRV. In the current investigation by identifying the elemental components of PM2.5, we observed an association between increased individual PM2.5 metal exposures, specifically manganese, and declines in night rMSSD. We observed heterogeneous associations across the different metals with statistically significant (p < 0.05), declines in HRV per 1 μg/m3 increase aluminum, iron and manganese.
Since PM2.5 and metal exposures were correlated, we confirmed the results with residual models. The residual method of analysis confirmed the manganese effect: a -0.250 (95% CI: -0.331, -0.169) msec change in night rMSSD was observed with every 1 μg/m3 increase in manganese residual, which is manganese independent of PM2.5 mass. An inverse exposure-response relationship was also confirmed for aluminum, chromium, and lead exposures. Expressed per increase in interquartile range of exposure, the largest decline in HRV was seen for manganese. Since the metal residual was no longer correlated with PM2.5, we were able to explore the effect of increasing metal exposures while holding PM2.5 constant by adjusting for PM2.5 in the metal residual models. We found that after adjusting for PM2.5, an inverse relationship, similar in magnitude, persisted for residual manganese, although the confidence intervals were broad.
The association between total PM2.5 exposures and night HRV observed in this study is consistent with our previous report among this population . As we hypothesized, unlike the study by Magari et al.  that evaluated daytime HRV over work, this study used the susceptible night period and we observed a negative association between night HRV and PM2.5 metal exposures. However, a study of highway patrol troopers observed a positive association with increases in post-shift HRV with a source factor related to speed-changing traffic which was dominated by copper, aldehyde and sulfur content of PM2.5 exposures . In both our previous investigation and the patrol trooper study the timing of HRV response occurs during or immediately post-exposure; unlike the current study, where HRV was measured in the evening following workday exposure. These disparate results may be capturing the varying time-course of metal responses or the complex interplay between different metals, which is supported by toxicological studies.
While the exact mechanism is unknown, once transition metal components of PM2.5 are delivered to the airways, they may catalyze the production of reactive oxygen species (ROS), which cause airway injury and inflammation and start a cascade of pulmonary and cardiac responses . This proposed mechanism is supported in part by in vitro and in vivo studies showing an association between transition metal exposures and generation of ROS , and an association between transition metal exposures and cardiovascular autonomic changes in mice  and rats  yet not dogs . Alternately, other metals such as zinc has been shown to trigger effects by directly interacting with cellular proteins [20, 21].
Results from our current study signal the cardiotoxicity of manganese. Both the standard and residual models presented an inverse exposure-response relationship for manganese and effects persisted after adjustment for total PM2.5 exposure suggesting that manganese effects are independent of total fine particulate matter effects. While the cardiotoxicity of manganese has not been previously reported, manganese neurotoxicities are well recognized, and both epidemiological and toxicological studies suggest that manganese exposure may also lead to cardiovascular toxicities . Abnormal ECG parameters, including sinus arrhythmia and ST-T changes, are increased in workers exposed to manganese oxide as compared to controls  and Barrington et al. report decreased autonomic function and low 24-hr HRV, in manganese alloy workers, though this association has yet to be corroborated by in vivo studies, as no significant HRV changes in dogs were observed subsequent to short-term inhalation of aerosol manganese .
Yet, metal content does not completely explain the declines in HRV observed within this cohort. An inverse association was observed with PM2.5 in the residual models adjusted for individual metals, although PM2.5 was not significant in the manganese model. For these metals, this suggests that when the metal content is held constant, there remains a total PM2.5 exposure effect. We were unable to determine which, if any, chemical component this is due to. However, the non-metal components may also play a role in the observed cardiotoxicity of PM2.5 exposures. In fact, we investigated the association between PM2.5 silicon exposures and night rMSSD and observed a -0.17 (95% CI: -0.24, -0.10) msec change per 1 μg/m3 increase in silicon PM2.5 exposure after adjusting for non-work HRV and smoking status. The silicon association was attenuated after controlling for PM2.5 mass; -0.10 (95% CI: -0.53, 0.33). Due to limitations in the XRF analysis technique, we were unable to measure the silicon complex within the welding fume, however previous investigation of welding fume exposure suggests that silicon is likely in the silica state . Decreases in HRV with silica exposures have been previously observed in a study of aged, ApoE knockout transgenic mice where both ambient particulate matter or silica produced decreases in HRV parameters . The health effects of occupational silica exposure are well recognized; both acute and chronic silica exposures, in the form of crystalline silica, can lead to silicosis, a debilitating fibrotic disease of the lung. Silica exposure has been linked to inflammation and autoimmune diseases . The cardio-toxicity of silica exposure warrants further research.
While we observed signals of cardiotoxicity for manganese, we did not observe an effect for nickel, which has previously been implicated in changes in heart rate and HRV . It is unlikely that one component of PM is responsible for all cardiovascular effects and it is unclear what role the composition mixtures play. One major limitation of this study is the exposure source, which differs substantially from ambient PM2.5 or other sources of PM2.5. While welding fumes are enhanced in some metals, they may have lower than average proportions of other metals, which may be relevant for other exposure scenarios, and may explain differences in study results. Therefore, the generalizability of the current study results to ambient air pollution exposures is limited.
This study is strengthened by detailed exposure assessment with personal PM2.5 exposure monitoring with elemental determination. In total, the elemental mass determined by XRF analysis accounted for 56% of the sample mass. However, one limitation of XRF analysis is that it cannot discern metal oxidation states or identify metals complexes. While the welding fume metals are likely present as metal oxides, the solubility of each element, which may affect toxicity, remains unknown.
While the number of participants available for our study was small, the efficiency of the study was improved by the use of non-work monitoring. Each participant served as his own control by providing baseline, non-work HRV measures over the same time period as work measures. Baseline measures controlled for potential confounding by time-invariant, individual factors such as smoking, health status or general physical activity levels. While particle metal exposures were not monitored during non-work, as compared to workday welding fume exposures, the non-workday ambient metal exposures are likely to be negligible. This study is also strengthened by having separated the exposure period (occurring during work) and the outcome period (occurring in the evening after work) by time, which limits the potential for confounding. In addition to being time-varying, potential confounders must also be associated with exposure during the work time period and be predictors of HRV in the time following exposure. For example, while ventilation during work may be associated with exposure during the work period, it is not associated with night HRV several hours after exposure occurs. Although we were unable to account for predictors of HRV that might vary between the work and non-work periods, such as quantity of caffeine, alcohol and cigarette consumption, for the exposure-response analysis, we hypothesize that neither caffeine nor alcohol consumption were correlated with work PM2.5 exposure; therefore the potential for confounding bias by these factors is small. We adjusted for smoking by using a binary variable, but were unable to account for the quantity of cigarettes consumed. However, workers were allowed to smoke on the job, and it is unlikely that the quantity of cigarettes consumed differed between work and non-work periods. Semi-quantitative urinary cotinine levels obtained from NicAlert Strips  on a sub-set of the smokers confirmed that there was no difference between work and non-work smoking intensity. Thus, the likelihood of confounding by smoking is low. While the majority of the participants reported no health compromises, there were 8 who reported either or both hypertension or cardiac compromises and of these 3 individuals reported medication use, which could also vary with time. However, when we restricted the cohort to exclude the individuals reporting medication use, the manganese effect persisted in magnitude and increased in statistical significance. Due to small sample size, we were unable to investigate the potential modifying effects of hypertension or cardiac compromises. Since 81% of the non-workday monitoring occurred within the same week as workday monitoring, we were able to control for longer term time trends such as season.
Nevertheless, while we observed statistically significant results for manganese exposures, the lack of statistical significance in the relationships with other metals may be due, in part, to the small sample size. Lastly, the mechanism of metal-related cardiovascular toxicity may be complex and while we observed signals of toxicity in the night period, it is possible that we did not capture early or later effects.
In summary, this study supports the cardiotoxicity of the metal component of particulate matter exposures. There appears to be a difference in cardiac autonomic response among the metals with a consistent exposure-response relationship observed for manganese. Yet, results suggest the importance of other metal and non-metal particulate matter components in the observed cardiovascular autonomic effects.
This research was supported by NIEHS grants ES009860 and ES00002. JMC was supported by T32 ES 07069, T42 OH008416, and the Taplin Fellowship. The authors thank P Boyce, C Dobson, JY Kim, S Magari, A Mehta, E Rodrigues, L Su, M Wang and the International Brotherhood of Boilermakers, Local 29, Quincy, MA.
- Pope CA, Dockery DW: Health effects of fine particulate air pollution: lines that connect. J Air Waste Manag Assoc. 2006, 56 (6): 709-742.View ArticleGoogle Scholar
- Peters A: Particulate matter and heart disease: Evidence from epidemiological studies. Toxicol Appl Pharmacol. 2005, 207 (2 Suppl): 477-482. 10.1016/j.taap.2005.04.030.View ArticleGoogle Scholar
- Schulz H, Harder V, Ibald-Mulli A, Khandoga A, Koenig W, Krombach F, Radykewicz R, Stampfl A, Thorand B, Peters A: Cardiovascular effects of fine and ultrafine particles. J Aerosol Med. 2005, 18 (1): 1-22. 10.1089/jam.2005.18.1.View ArticleGoogle Scholar
- Schwarze PE, Ovrevik J, Lag M, Refsnes M, Nafstad P, Hetland RB, Dybing E: Particulate matter properties and health effects: consistency of epidemiological and toxicological studies. Hum Exp Toxicol. 2006, 25 (10): 559-579. 10.1177/096032706072520.View ArticleGoogle Scholar
- Brook RD: Is air pollution a cause of cardiovascular disease? Updated review and controversies. Rev Environ Health. 2007, 22 (2): 115-137.View ArticleGoogle Scholar
- Adar SD, Kaufman JD: Cardiovascular disease and air pollutants: evaluating and improving epidemiological data implicating traffic exposure. Inhal Toxicol. 2007, 19 Suppl 1: 135-149. 10.1080/08958370701496012.View ArticleGoogle Scholar
- Schlesinger RB, Kunzli N, Hidy GM, Gotschi T, Jerrett M: The health relevance of ambient particulate matter characteristics: coherence of toxicological and epidemiological inferences. Inhal Toxicol. 2006, 18 (2): 95-125. 10.1080/08958370500306016.View ArticleGoogle Scholar
- Park SK, O'Neill MS, Wright RO, Hu H, Vokonas PS, Sparrow D, Suh H, Schwartz J: HFE genotype, particulate air pollution, and heart rate variability: a gene-environment interaction. Circulation. 2006, 114 (25): 2798-2805. 10.1161/CIRCULATIONAHA.106.643197.View ArticleGoogle Scholar
- Magari SR, Hauser R, Schwartz J, Williams P, Smith TJ, Christiani DC: The association of particulate air metal concentrations with heart rate variability. Environ Health Perspect. 2002, 110 (9): 875-880.View ArticleGoogle Scholar
- Cavallari JM, Eisen EA, Chen JC, Fang SC, Dobson CB, Schwartz J, Christiani DC: Night heart rate variability and particulate exposures among boilermaker construction workers. Environ Health Perspect. 2007, 115 (7): 1046-1051.View ArticleGoogle Scholar
- Chow J, Watson J: Guidelines on speciated particulate monitoring, third draft report. 1998, Research Triangle Park, NC , U.S. Environmental Protection Agency, Office of Air Quality Planning and StandardsGoogle Scholar
- Watson J, Chow J, Frazier C: X-ray fluorescence analysis of ambient air samples. Elemental Analysis of Airborne Particles. Edited by: Landberger SCM. 1999, NJ , Gordon and Breach Publishers, 67-96.Google Scholar
- Willett WC, Howe GR, Kushi LH: Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr. 1997, 65 (4 Suppl): 1220S-1228S; discussion 1229S-1231S.Google Scholar
- Riediker M, Devlin RB, Griggs TR, Herbst MC, Bromberg PA, Williams RW, Cascio WE: Cardiovascular effects in patrol officers are associated with fine particulate matter from brake wear and engine emissions. Part Fibre Toxicol. 2004, 1 (1): 2-10.1186/1743-8977-1-2.View ArticleGoogle Scholar
- Gonzalez-Flecha B: Oxidant mechanisms in response to ambient air particles. Mol Aspects Med. 2004, 25 (1-2): 169-182. 10.1016/j.mam.2004.02.017.View ArticleGoogle Scholar
- Maciejczyk P, Chen LC: Effects of subchronic exposures to concentrated ambient particles (CAPs) in mice. VIII. Source-related daily variations in in vitro responses to CAPs. Inhal Toxicol. 2005, 17 (4-5): 243-253. 10.1080/08958370590912914.View ArticleGoogle Scholar
- Lippmann M, Ito K, Hwang JS, Maciejczyk P, Chen LC: Cardiovascular effects of nickel in ambient air. Environ Health Perspect. 2006, 114 (11): 1662-1669.Google Scholar
- Campen MJ, Nolan JP, Schladweiler MC, Kodavanti UP, Evansky PA, Costa DL, Watkinson WP: Cardiovascular and thermoregulatory effects of inhaled PM-associated transition metals: a potential interaction between nickel and vanadium sulfate. Toxicol Sci. 2001, 64 (2): 243-252. 10.1093/toxsci/64.2.243.View ArticleGoogle Scholar
- Muggenburg BA, Benson JM, Barr EB, Kubatko J, Tilley LP: Short-term inhalation of particulate transition metals has little effect on the electrocardiograms of dogs having preexisting cardiac abnormalities. Inhal Toxicol. 2003, 15 (4): 357-371. 10.1080/08958370304456.View ArticleGoogle Scholar
- Tal TL, Graves LM, Silbajoris R, Bromberg PA, Wu W, Samet JM: Inhibition of protein tyrosine phosphatase activity mediates epidermal growth factor receptor signaling in human airway epithelial cells exposed to Zn2+. Toxicol Appl Pharmacol. 2006, 214 (1): 16-23. 10.1016/j.taap.2005.11.011.View ArticleGoogle Scholar
- Haase H, Maret W: Protein tyrosine phosphatases as targets of the combined insulinomimetic effects of zinc and oxidants. Biometals. 2005, 18 (4): 333-338. 10.1007/s10534-005-3707-9.View ArticleGoogle Scholar
- Jiang Y, Zheng W: Cardiovascular toxicities upon manganese exposure. Cardiovasc Toxicol. 2005, 5 (4): 345-354. 10.1385/CT:5:4:345.View ArticleGoogle Scholar
- Barrington WW, Angle CR, Willcockson NK, Padula MA, Korn T: Autonomic function in manganese alloy workers. Environ Res. 1998, 78 (1): 50-58. 10.1006/enrs.1997.3826.View ArticleGoogle Scholar
- Antonini JM: Health effects of welding. Crit Rev Toxicol. 2003, 33 (1): 61-103. 10.1080/713611032.View ArticleGoogle Scholar
- Corey LM, Baker C, Luchtel DL: Heart-rate variability in the apolipoprotein E knockout transgenic mouse following exposure to Seattle particulate matter. J Toxicol Environ Health A. 2006, 69 (10): 953-965. 10.1080/15287390500362105.View ArticleGoogle Scholar
- Parks CG, Conrad K, Cooper GS: Occupational exposure to crystalline silica and autoimmune disease. Environ Health Perspect. 1999, 107 Suppl 5: 793-802. 10.2307/3434342.View ArticleGoogle Scholar
- Bernert JT, Harmon TL, Sosnoff CS, McGuffey JE: Use of continine immunoassay test strips for preclassifying urine samples from smokers and nonsmokers prior to analysis by LC-MS-MS. J Anal Toxicol. 2005, 29 (8): 814-818.View ArticleGoogle Scholar
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