Petroleum and Chlorinated Solvents in Meconium and the Risk of Hypospadias: A Pilot Study

Florence Rouget, Adèle Bihannic, Sylvaine Cordier, Luc Multigner, Marie Meyer-Monath, Fabien Mercier, Patrick Pladys, Ronan Garlantezec, Florence Rouget, Adèle Bihannic, Sylvaine Cordier, Luc Multigner, Marie Meyer-Monath, Fabien Mercier, Patrick Pladys, Ronan Garlantezec

Abstract

Background: Hypospadias is a male congenital malformation that occurs in ~2 of 1,000 births. The association between hypospadias and fetal exposure to environmental chemicals has been studied, but the results are inconsistent. Although several petroleum and chlorinated solvents are suspected to have teratogenic effects, their role in the occurrence of hypospadias has been little studied and never using biomarkers of exposure. We aimed to evaluate the association between fetal exposure to petroleum and chlorinated solvents measured in meconium and the occurrence of hypospadias. Methods: We conducted a pilot case-control study in the maternity of the University Hospital of Rennes (France). Eleven cases of hypospadias and 46 controls were recruited between October 2012 and January 2014. Data from hospital records and maternal self-reported questionnaires, including socio-demographic characteristics and occupational and non-occupational exposure to chemicals, were collected. Meconium samples were collected using a standardized protocol. Levels of petroleum solvents (toluene, benzene, ethylbenzene, and p, m, and o xylene), certain metabolites (mandelic acid, hippuric acid, methylhippuric acid, S-phenylmercapturic acid, S-benzylmercapturic acid, and phenylglyoxylic acid), and two chlorinated solvents (trichloroethylene and tetrachloroethylene) were measured in meconium by gas and liquid chromatography, both coupled to tandem mass spectrometry. Associations between the concentration of each chemical and the occurrence of hypospadias were analyzed using exact logistic regressions adjusted for maternal age, educational level, pre-pregnancy body mass index, and alcohol, and tobacco consumption during pregnancy. Results are presented with odds ratios (ORs) and their 95% confidence intervals (CIs). Results: Quantification rates for petroleum and chlorinated solvents or metabolites ranged from 2.2% (for methylhippuric acid) to 77.1% (for trichloroethylene) of the meconium samples. We found a significant association between the quantification of phenylglyoxylic acid (metabolite of styrene and ethylbenzene) in the meconium and a higher risk of hypospadias (OR = 14.2, 95% CI [2.5-138.7]). The risk of hypospadias was non-significantly elevated for most of the other solvents and metabolites. Conclusion: This exploratory study, on a limited number of cases, suggests an association between petroleum solvents and hypospadias. Additional studies are needed to confirm these results and identify the determinants for the presence of these solvents in meconium.

Keywords: BTEX; chlorinated solvents; hypospadias; meconium; petroleum solvents; volatile organic compound.

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Copyright © 2021 Rouget, Bihannic, Cordier, Multigner, Meyer-Monath, Mercier, Pladys and Garlantezec.

References

    1. Bergman JEH, Loane M, Vrijheid M, Pierini A, Nijman RJM, Addor M-C, et al. . Epidemiology of hypospadias in Europe: a registry-based study. World J Urol. (2015) 33:2159–67. 10.1007/s00345-015-1507-6
    1. Yu X, Nassar N, Mastroiacovo P, Canfield M, Groisman B, Bermejo-Sánchez E, et al. . Hypospadias prevalence and trends in international birth defect surveillance systems, 1980-2010. Eur Urol. (2019) 76:482–90. 10.1016/j.eururo.2019.06.027
    1. van der Zanden LF, van Rooij IA, Feitz WF, Franke B, Knoers NV, Roeleveld N. Aetiology of hypospadias: a systematic review of genes and environment. Hum Reprod Update. (2012) 18:260–83. 10.1093/humupd/dms002
    1. Toppari J, Virtanen HE, Main KM, Skakkebaek NE. Cryptorchidism and hypospadias as a sign of testicular dysgenesis syndrome (TDS): environmental connection. Birt Defects Res A Clin Mol Teratol. (2010) 88:910–9. 10.1002/bdra.20707
    1. Kalfa N, Paris F, Philibert P, Orsini M, Broussous S, Fauconnet-Servant N, et al. . Is hypospadias associated with prenatal exposure to endocrine disruptors? A French Collaborative Controlled Study of a Cohort of 300 Consecutive Children Without Genetic Defect. Eur Urol. (2015) 68:1023–30. 10.1016/j.eururo.2015.05.008
    1. Garlantézec R, Monfort C, Rouget F, Cordier S. Maternal occupational exposure to solvents and congenital malformations: a prospective study in the general population. Occup Environ Med. (2009) 66:456–63. 10.1136/oem.2008.041772
    1. Aschengrau A, Gallagher LG, Winter M, Butler L, Patricia Fabian M, Vieira VM. Modeled exposure to tetrachloroethylene-contaminated drinking water and the occurrence of birth defects: a case-control study from Massachusetts and Rhode Island. Environ Health. (2018) 17:75. 10.1186/s12940-018-0419-5
    1. Spinder N, Prins JR, Bergman JEH, Smidt N, Kromhout H, Boezen HM, et al. . Congenital anomalies in the offspring of occupationally exposed mothers: a systematic review and meta-analysis of studies using expert assessment for occupational exposures. Hum Reprod. (2019) 34:903–19. 10.1093/humrep/dez033
    1. Haraux E, Braun K, Buisson P, Stéphan-Blanchard E, Devauchelle C, Ricard J, et al. . Maternal exposure to domestic hair cosmetics and occupational endocrine disruptors is associated with a higher risk of hypospadias in the offspring. Int J Environ Res Public Health. 29. (2016) 14:27. 10.3390/ijerph14010027
    1. Cordier S, Garlantézec R, Labat L, Rouget F, Monfort C, Bonvallot N, et al. . Exposure during pregnancy to glycol ethers and chlorinated solvents and the risk of congenital malformations. Epidemiol Camb Mass. (2012) 23:806–12. 10.1097/EDE.0b013e31826c2bd8
    1. Warembourg C, Botton J, Lelong N, Rouget F, Khoshnood B, Le Gléau F, et al. . Prenatal exposure to glycol ethers and cryptorchidism and hypospadias: a nested case-control study. Occup Environ Med. (2018) 75:59–65. 10.1136/oemed-2017-104391
    1. Bolden AL, Kwiatkowski CF, Colborn T. New look at BTEX: are ambient levels a problem? Environ Sci Technol. (2015) 49:5261–76. 10.1021/es505316f
    1. Bearer CF. Meconium as a biological marker of prenatal exposure. Ambul Pediatr Off J Ambul Pediatr Assoc. (2003) 3:40–3. 10.1367/1539-4409(2003)003<0040:MAABMO>;2
    1. Lisowska-Myjak B, Skarzyńska E, Wojdan K, Nasierowska-Guttmejer A. Protein and peptide profiles in neonatal meconium. J Obstet Gynaecol Res. (2019) 45:556–64. 10.1111/jog.13888
    1. Arbuckle TE. Maternal-infant biomonitoring of environmental chemicals: the epidemiologic challenges. Birt Defects Res A Clin Mol Teratol. (2010) 88:931–7. 10.1002/bdra.20694
    1. Moore C, Negrusz A, Lewis D. Determination of drugs of abuse in meconium. J Chromatogr B Biomed Sci App. (1998) 713:137–46. 10.1016/S0378-4347(97)00479-9
    1. Ostrea EM, Bielawski DM, Posecion NC, Corrion M, Villanueva-Uy E, Bernardo RC, et al. . Combined analysis of prenatal (maternal hair and blood) and neonatal (infant hair, cord blood and meconium) matrices to detect fetal exposure to environmental pesticides. Environ Res. (2009) 109:116–22. 10.1016/j.envres.2008.09.004
    1. Berton T, Mayhoub F, Chardon K, Duca R-C, Lestremau F, Bach V, et al. . Development of an analytical strategy based on LC-MS/MS for the measurement of different classes of pesticides and theirs metabolites in meconium: application and characterisation of foetal exposure in France. Environ Res. (2014) 132:311–20. 10.1016/j.envres.2014.03.034
    1. Haraux E, Tourneux P, Kouakam C, Stephan-Blanchard E, Boudailliez B, Leke A, et al. . Isolated hypospadias: the impact of prenatal exposure to pesticides, as determined by meconium analysis. Environ Int. (2018) 119:20–5. 10.1016/j.envint.2018.06.002
    1. Li L-X, Chen L, Meng X-Z, Chen B-H, Chen S-Q, Zhao Y, et al. . Exposure levels of environmental endocrine disruptors in mother-newborn pairs in China and their placental transfer characteristics. PLoS One. (2013) 8:e62526. 10.1371/journal.pone.0062526
    1. EUROCAT-JRC . EUROCAT Guide 1.4: Instruction for the Registration of Congenital Anomalies. (2020). Available online at: (accessed November 12, 2020).
    1. Pilorget C, Dananché B, Luce D, Févotte J, the Matgéné working group . Éléments Techniques Sur L'exposition Professionnelle Aux Carburants et Solvants Pétroliers. Matrice Emplois-Expositions Aux Carburants et Solvants Pétroliers. Saint-Maurice: InVS Umrestte Lyon (2007). Available online at : (accessed November 12, 2020).
    1. Dananché B, Févotte J, the Matgéné working group . Éléments Techniques Sur L'exposition Professionnelle à Cinq Solvants Chlorés (Trichloroéthylène, Perchloroéthylène, Chlorure de Méthylène, Tétrachlorure de Carbone, Chloroforme) - Matrices Emploisexpositions à Cinq Solvants Chlorés. Saint-Maurice (Fra): Institut de veille sanitaire - Umrestte Lyon (2009). 29 p. Available online at : (accessed November 12, 2020).
    1. Meyer-Monath M, Beaumont J, Morel I, Rouget F, Tack K, Lestremau F. Analysis of BTEX and chlorinated solvents in meconium by headspace-solid-phase microextraction gas chromatography coupled with mass spectrometry. Anal Bioanal Chem. (2014) 406:4481–90. 10.1007/s00216-014-7836-2
    1. Meyer-Monath M, Chatellier C, Rouget F, Morel I, Lestremau F. Development of a multi-residue method in a fetal matrix: analysis of meconium. Anal Bioanal Chem. (2014) 406:7785–97. 10.1007/s00216-014-8243-4
    1. Maiti T, Pradhan V. A comparative study of the bias corrected estimates in logistic regression. Stat Methods Med Res. (2008) 17:621–34. 10.1177/0962280207084156
    1. Rothman KJ, Greenland S, Las TL. Modern Epidemiology, 3rd edn. Philadelphia, PA: Lippincott Williams & Wilkins; (2008).
    1. Bender R, Lange S. Adjusting for multiple testing–when and how? J Clin Epidemiol. (2001) 54:343–9. 10.1016/S0895-4356(00)00314-0
    1. Barr DB, Wang RY, Needham LL. Biologic monitoring of exposure to environmental chemicals throughout the life stages: requirements and issues for consideration for the National Children's Study. Environ Health Perspect. (2005) 113:1083–91. 10.1289/ehp.7617
    1. Baskin L, Cao M, Sinclair A, Li Y, Overland M, Isaacson D, et al. . Androgen and estrogen receptor expression in the developing human penis and clitoris. Differ Res Biol Divers. (2020) 111:41–59. 10.1016/j.diff.2019.08.005
    1. Li Y, Sinclair A, Cao M, Shen J, Choudhry S, Botta S, et al. . Canalization of the urethral plate precedes fusion of the urethral folds during male penile urethral development: the double zipper hypothesis. J Urol. (2015) 193:1353–60. 10.1016/j.juro.2014.09.108
    1. Chambers DM, Ocariz JM, McGuirk MF, Blount BC. Impact of cigarette smoking on volatile organic compound (VOC) blood levels in the U.S. population: NHANES 2003-2004. Environ Int. (2011) 37:1321–8. 10.1016/j.envint.2011.05.016
    1. Fustinoni S, Rossella F, Campo L, Mercadante R, Bertazzi PA. Urinary BTEX, MTBE and naphthalene as biomarkers to gain environmental exposure profiles of the general population. Sci Total Environ. (2010) 408:2840–9. 10.1016/j.scitotenv.2010.03.017
    1. Protano C, Andreoli R, Manini P, Vitali M. Urinary trans, trans-muconic acid and S-phenylmercapturic acid are indicative of exposure to urban benzene pollution during childhood. Sci Total Environ. (2012) 435–436:115–23. 10.1016/j.scitotenv.2012.07.004
    1. Capella KM. Ethylbenzene and styrene exposure in the United States based on urinary mandelic acid and phenylglyoxylic acid_NHANES 2005-2006 and 2011-2012. Environ Res. (2019) 171:101–10. 10.1016/j.envres.2019.01.018
    1. Skender L, Brcić I, Karacić V. Urine analysis for the evaluation of environmental exposures to aromatic hydrocarbons. Arch Environ Health. (2004) 59:237–44. 10.3200/AEOH.59.5.237-244
    1. Mohamed MF, Kang D, Aneja VP. Volatile organic compounds in some urban locations in United States. Chemosphere. (2002) 47:863–82. 10.1016/S0045-6535(02)00107-8
    1. Barros N, Carvalho M, Silva C, Fontes T, Prata JC, Sousa A, et al. . Environmental and biological monitoring of benzene, toluene, ethylbenzene and xylene (BTEX) exposure in residents living near gas stations. J Toxicol Environ Health A. (2019) 82:550–63. 10.1080/15287394.2019.1634380
    1. Symanski E, Stock TH, Tee PG, Chan W. Demographic, residential, and behavioral determinants of elevated exposures to benzene, toluene, ethylbenzene, and xylenes among the U.S. population: results from 1999-2000 NHANES. J Toxicol Environ Health A. (2009) 72:915–24. 10.1080/15287390902959706
    1. Cao X-L, Sparling M, Dabeka R. Occurrence of 13 volatile organic compounds in foods from the Canadian total diet study. Food Addit Contam Part Chem Anal Control Expo Risk Assess. (2016) 33:373–82. 10.1080/19440049.2015.1129072
    1. Ohyama K-I, Satoh K, Sakamoto Y, Ogata A, Nagai F. Effects of prenatal exposure to styrene trimers on genital organs and hormones in male rats. Exp Biol Med Maywood NJ. (2007) 232:301–8. 10.3181/00379727-207-2320301
    1. Cao X-L, Sparling M, Pelletier L, Dabeka R. Styrene in foods and dietary exposure estimates. Food Addit Contam Part Chem Anal Control Expo Risk Assess. (2018) 35:2045–51. 10.1080/19440049.2018.1512760
    1. Wheeler AJ, Wong SL, Khoury C, Zhu J. Predictors of indoor BTEX concentrations in Canadian residences. Health Rep. (2013) 24:9.
    1. ANSES . Sécurité des Couches Pour Bébé. Rapport D'expertise Collective (2019). Available online at: (accessed November 12, 2020).
    1. National Center for Biotechnology Information . PubChem Compound Summary for CID 11915, Benzoylformic Acid. Available online at: (accessed November 12, 2020).
    1. Mirkova E, Zaikov C, Antov G, Mikhailova A, Khinkova L, Benchev I. Prenatal toxicity of xylene. J Hyg Epidemiol Microbiol Immunol. (1983) 27:337–43.
    1. Marks TA, Ledoux TA, Moore JA. Teratogenicity of a commercial xylene mixture in the mouse. J Toxicol Environ Health. (1982) 9:97–105. 10.1080/15287398209530145
    1. Saillenfait AM, Gallissot F, Morel G, Bonnet P. Developmental toxicities of ethylbenzene, ortho-, meta-, para-xylene and technical xylene in rats following inhalation exposure. Food Chem Toxicol. (2003) 41:415–29. 10.1016/S0278-6915(02)00231-4
    1. Vainio H, Hemminki K, Elovaara E. Toxicity of styrene and styrene oxide on chick embryos. Toxicology. (1977) 8:319–25. 10.1016/0300-483X(77)90079-8
    1. Sikov MR, Cannon WC, Carr DB, Miller RA, Niemeier RW, Hardin BD. Reproductive toxicology of inhaled styrene oxide in rats and rabbits. J Appl Toxicol JAT. (1986) 6:155–64. 10.1002/jat.2550060304
    1. Urban JD, Wikoff DS, Chappell GA, Harris C, Haws LC. Systematic evaluation of mechanistic data in assessing in utero exposures to trichloroethylene and development of congenital heart defects. Toxicology. (2020) 436:152427. 10.1016/j.tox.2020.152427
    1. Hardin BD, Kelman BJ, Brent RL. Trichloroethylene and dichloroethylene: a critical review of teratogenicity. Birt Defects Res A Clin Mol Teratol. (2005) 73:931–55. 10.1002/bdra.20192
    1. Bolden AL, Schultz K, Pelch KE, Kwiatkowski CF. Exploring the endocrine activity of air pollutants associated with unconventional oil and gas extraction. Environ Health. (2018) 17:26. 10.1186/s12940-018-0368-z
    1. The Agency for Toxic Substances and Disease Registry (ATSDR) . Toxicological Profile for Ethylbenzene. (2010). Available online at: (accessed November 12, 2020).

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