Abstract
Phthalate exposure has been reported to be associated with obesity (measured by body mass index [BMI]) and central obesity (measured by waist circumference [WC]). Yet, reported associations and the potential gender and age differences are inconsistent. We conducted a cross-sectional study involving 2330 participants in the fall of 2012. Urinary metabolites of ten phthalates were measured. Height, body weight, and waist circumference (WC) were measured using standardized methods. We performed logistic regression analyses to estimate the association between each urine phthalate metabolite (categorized into quartiles) and obesity and central obesity and conducted an additional, stratified analysis to explore the gender and age differences. In the overall study population, higher urinary levels of MMP, MEHHP, and MECPP were associated with increased ratios of central obesity. When stratifying by gender and central obesity, higher urinary levels of MMP, MEHHP, and MEOHP were associated with increased odds of central obesity in females, whereas MBzP was significantly associated inversely with central obesity in females. In males, it showed no significant P value for trend (P trend). When stratifying by age in females, higher urinary levels of MEHP, MEOHP, MEHHP, and MECPP were associated with increased odds of central obesity in women aged ≤45 years. In females aged >45 years, it showed no significant P trend. In conclusion, we found that association between phthalates and central obesity was stronger than between phthalates and obesity; association between phthalates and central obesity was stronger in females than in males and was stronger in younger females (aged ≤45 years) than in older females (aged >45 years).
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.References
Akin F, Bastemir M, Alkis E, Kaptanoglu B (2009) SHBG levels correlate with insulin resistance in postmenopausal women. Eur J Intern Med 20(2):162–167. doi:10.1016/j.ejim.2007.09.023
Barr DB, Wilder LC, Caudill SP et al (2005) Urinary creatinine concentrations in the U.S. population: implications for urinary biologic monitoring measurements. Environ Health Perspect 113(2):192–200
Bjorntorp P (1996) The regulation of adipose tissue distribution in humans. Int J Obes Relat Metab Disord 20(4):291–302
Bornehag CG, Sundell J, Weschler CJ (2004) The association between asthma and allergic symptoms in children and phthalates in house dust: a nested case-control study. Environ Health Perspect 112(14):1393–1397
Buser MC, Murray HE, Scinicariello F (2014) Age and sex differences in childhood and adulthood obesity association with phthalates: analyses of NHANES 2007–2010. Int J Hyg Environ Health 217(6):687–694. doi:10.1016/j.ijheh.2014.02.005
Cui R, Qi Z, Zhou L et al (2016) Evaluation of serum lipid profile, body mass index, waistline in Chinese patients with type 2 diabetes mellitus. Clin Interv Aging 11:445–452. doi:10.2147/CIA.S104803
Diamanti-Kandarakis E, Bourguignon JP (2009) Endocrine-disrupting chemicals: an Endocrine Society scientific statement. Endocr Rev 30(4):293–342. doi:10.1210/er.2009-0002
Dong R, Zhou T, Zhao S et al (2017) Food consumption survey of Shanghai adults in 2012 and its associations with phthalate metabolites in urine. Environ Int. doi:10.1016/j.envint.2017.01.008
Feige JN, Gelman L, Rossi D et al (2007) The endocrine disruptor monoethyl-hexyl-phthalate is a selective peroxisome proliferator-activated receptor gamma modulator that promotes adipogenesis. J Biol Chem 282(26):19152–19166. doi:10.1074/jbc.M702724200
Ferguson KK, Cantonwine DE, Rivera-Gonzalez LO et al (2014) Urinary phthalate metabolite associations with biomarkers of inflammation and oxidative stress across pregnancy in Puerto Rico. Environ Sci Technol 48(12):7018–7025. doi:10.1021/es502076j
Fromme H, Bolte G, Koch HM et al (2007) Occurrence and daily variation of phthalate metabolites in the urine of an adult population. Int J Hyg Environ Health 210(1):21–33. doi:10.1016/j.ijheh.2006.09.005
Gapstur SM, Gann PH, Kopp P et al (2002) Serum androgen concentrations in young men: a longitudinal analysis of associations with age, obesity, and race. The CARDIA male hormone study. Cancer Epidemiol Biomarkers Prev 11(10 Pt 1):1041–1047
Grun F, Blumberg B (2007) Perturbed nuclear receptor signaling by environmental obesogens as emerging factors in the obesity crisis. Rev Endocr Metab Disord 8(2):161–171. doi:10.1007/s11154-007-9049-x
Hatch EE, Nelson JW, Qureshi MM et al (2008) Association of urinary phthalate metabolite concentrations with body mass index and waist circumference: a cross-sectional study of NHANES data, 1999–2002. Environ Health 7:27. doi:10.1186/1476-069X-7-27
Hatch EE, Nelson JW, Stahlhut RW, Webster TF (2010) Association of endocrine disruptors and obesity: perspectives from epidemiological studies. Int J Androl 33(2):324–332. doi:10.1111/j.1365-2605.2009.01035.x
Hauser R, Calafat AM (2005) Phthalates and human health. Occup Environ Med 62(11):806–818. doi:10.1136/oem.2004.017590
James-Todd TM, Huang T, Seely EW, Saxena AR (2016) The association between phthalates and metabolic syndrome: the National Health and Nutrition Examination Survey 2001–2010. Environ Health 15:52. doi:10.1186/s12940-016-0136-x
Latini G, Scoditti E, Verrotti A et al (2008) Peroxisome proliferator-activated receptors as mediators of phthalate-induced effects in the male and female reproductive tract: epidemiological and experimental evidence. PPAR Res 2008:359267. doi:10.1155/2008/359267
Lind PM, Lind L (2011) Circulating levels of bisphenol A and phthalates are related to carotid atherosclerosis in the elderly. Atherosclerosis 218(1):207–213. doi:10.1016/j.atherosclerosis.2011.05.001
Lind PM, Roos V, Ronn M et al (2012) Serum concentrations of phthalate metabolites are related to abdominal fat distribution two years later in elderly women. Environ Health 11:21. doi:10.1186/1476-069X-11-21
Main KM, Mortensen GK, Kaleva MM et al (2006) Human breast milk contamination with phthalates and alterations of endogenous reproductive hormones in infants three months of age. Environ Health Perspect 114(2):270–276
Martino-Andrade AJ, Chahoud I (2010) Reproductive toxicity of phthalate esters. Mol Nutr Food Res 54(1):148–157. doi:10.1002/mnfr.200800312
Meeker JD, Calafat AM, Hauser R (2007) Di(2-ethylhexyl) phthalate metabolites may alter thyroid hormone levels in men. Environ Health Perspect 115(7):1029–1034. doi:10.1289/ehp.9852
Pan G, Hanaoka T, Yoshimura M et al (2006) Decreased serum free testosterone in workers exposed to high levels of di-n-butyl phthalate (DBP) and di-2-ethylhexyl phthalate (DEHP): a cross-sectional study in China. Environ Health Perspect 114(11):1643–1648
Serrano SE, Braun J, Trasande L et al (2014) Phthalates and diet: a review of the food monitoring and epidemiology data. Environ Health 13(1):43. doi:10.1186/1476-069X-13-43
Silva MJ, Barr DB, Reidy JA et al (2004) Urinary levels of seven phthalate metabolites in the U.S. population from the National Health and Nutrition Examination Survey (NHANES) 1999–2000. Environ Health Perspect 112(3):331–338
Stahlhut RW, van Wijngaarden E, Dye TD et al (2007) Concentrations of urinary phthalate metabolites are associated with increased waist circumference and insulin resistance in adult U.S. males. Environ Health Perspect 115(6):876–882. doi:10.1289/ehp.9882
Swan SH (2008) Environmental phthalate exposure in relation to reproductive outcomes and other health endpoints in humans. Environ Res 108(2):177–1784
Swan SH, Main KM, Liu F et al (2005) Decrease in anogenital distance among male infants with prenatal phthalate exposure. Environ Health Perspect 113(8):1056–1061
Tchernof A, Despres JP (2000) Sex steroid hormones, sex hormone-binding globulin, and obesity in men and women. Horm Metab Res 32(11–12):526–536. doi:10.1055/s-2007-978681
Teitelbaum SL, Mervish N, Moshier EL et al (2012) Associations between phthalate metabolite urinary concentrations and body size measures in New York City children. Environ Res 112:186–193. doi:10.1016/j.envres.2011.12.006
Thayer KA, Heindel JJ, Bucher JR, Gallo MA (2012) Role of environmental chemicals in diabetes and obesity: a National Toxicology Program workshop review. Environ Health Perspect 120(6):779–789. doi:10.1289/ehp.1104597
Wang C, Jackson G, Jones TH et al (2011) Low testosterone associated with obesity and the metabolic syndrome contributes to sexual dysfunction and cardiovascular disease risk in men with type 2 diabetes. Diabetes Care 34(7):1669–1675. doi:10.2337/dc10-2339
Wang H, Zhou Y, Tang C et al (2013) Urinary phthalate metabolites are associated with body mass index and waist circumference in Chinese school children. PLoS ONE 8(2):e56800. doi:10.1371/journal.pone.0056800
Wisse BE (2004) The inflammatory syndrome: the role of adipose tissue cytokines in metabolic disorders linked to obesity. J Am Soc Nephrol 15(11):2792–2800. doi:10.1097/01.ASN.0000141966.69934.21
Wittassek M, Angerer J, Kolossa-Gehring M et al (2009) Fetal exposure to phthalates—a pilot study. Int J Hyg Environ Health 212(5):492–498. doi:10.1016/j.ijheh.2009.04.001
Wormuth M, Scheringer M, Vollenweider M, Hungerbuhler K (2006) What are the sources of exposure to eight frequently used phthalic acid esters in Europeans? Risk Anal 26(3):803–824. doi:10.1111/j.1539-6924.2006.00770.x
Yaghjyan L, Sites S, Ruan Y, Chang SH (2015) Associations of urinary phthalates with body mass index, waist circumference and serum lipids among females: national Health and Nutrition Examination Survey 1999–2004. Int J Obes (Lond) 39(6):994–1000. doi:10.1038/ijo.2015.8
Yassin A, Doros G (2013) Testosterone therapy in hypogonadal men results in sustained and clinically meaningful weight loss. Clin Obes 3(3–4):73–83. doi:10.1111/cob.12022
Zhang Y, Meng X, Chen L et al (2014) Age and sex-specific relationships between phthalate exposures and obesity in Chinese children at puberty. PLoS ONE 9(8):e104852. doi:10.1371/journal.pone.0104852
Zhou B (2002) Force coorperative meta-analysis group of china obesity task. Predictive values of body mass index and waist circumference to risk factors of related diseases in Chinese adult population. Zhonghua Liu Xing Bing Xue Za Zhi 23(1):5–10
Funding
This work was supported by the National Key Research and Development Program of China (No. 2016YFD0400602) and a fund from the National Natural Science Foundation of China (No. 81202208).
Author’s contributions
SL and BC contributed to conception and study design; RD, HZ, MZ, JC, and LZ contributed to acquisition of data; RD, TZ, and MW performed data analysis; RD, LZ, and BC contributed to interpretation of data; RD, LZ, and BC contributed to manuscript writing, and LZ, SL, and BC critically revised the manuscript. All authors read and approved the final manuscript.
Author information
Authors and Affiliations
Corresponding authors
Ethics declarations
Conflicts of interest
The authors declare that they have no conflict of interest.
Ethics Approval and Consent to Participate
All subjects submitted written, informed consent before their participation in the survey. The study was approved by the local authorities and the Ethics Committee of School of Public Health at Fudan University (IRB#2011-03-0264).
Rights and permissions
About this article
Cite this article
Dong, R., Zhou, T., Chen, J. et al. Gender- and Age-Specific Relationships Between Phthalate Exposures and Obesity in Shanghai Adults. Arch Environ Contam Toxicol 73, 431–441 (2017). https://doi.org/10.1007/s00244-017-0441-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00244-017-0441-6