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Common Endocrine-Disrupting Chemicals and Womenb s Health

It's quite astonishing how a wide array of chemicals found both in our surroundings and consumer products can cast an impact on female reproductive health.

These chemicals, known as endocrine-disrupting chemicals (EDCs), have been identified as potential disruptors that link to concerns like early puberty, complications in pregnancy duration, and various reproductive abnormalities. 

Picture this: a myriad of chemicals present in our surroundings and everyday products, subtly weaving their influence into the delicate fabric of female reproductive health. These chemicals, known as endocrine-disrupting chemicals (EDCs), have emerged as a group of compounds raising eyebrows due to their potential to disrupt the harmonious dance of hormones governing vital aspects like early puberty, pregnancy complexities, and other reproductive abnormalities. ??

The Unravelling of EDCs: A Complex Tale
EDCs hail from a multitude of sources, spanning industrial processes, agricultural practices, residential goods, and even pharmaceutical compounds. These elusive actors infiltrate our lives through channels as diverse as inhalation, dietary consumption, and direct contact. Interestingly, even heavy metals such as cadmium, lead, and mercury find themselves entangled in this intricate web.

Of particular note is the impact of personal care products, often marketed to women, as a notable source of EDC exposure. Think bisphenols, parabens, benzophenones, and phthalates – these are common culprits found in such products. What's intriguing is that young women aged 18 to 34, a demographic frequently drawn to an array of personal care items, may inadvertently subject themselves to these chemicals' influences.

The Timing Factor: Vulnerable Phases
Here's where timing comes into play. Women and their offspring may find themselves at a heightened vulnerability to EDC effects during sensitive life phases, including preconception and pregnancy. These chemicals can wield their influence on crucial hormonal pathways, potentially contributing to concerns like early onset of menstruation (menarche) and even conditions like polycystic ovarian syndrome (PCOS).

The Complex Web Unveiled
Peering into the vast realm of research uncovers a tapestry woven with intricate threads. While phenolic 2,5-DCP from dichlorobenzene, often used as a fumigant, has been implicated in early menarche, it's essential to recognize that this is merely a snapshot. An entire gamut of endocrine disruptors coexists within our environment, playing various roles in shaping this complex narrative.

Bisphenol molecules 

Diving into the intricate world of reproductive health, we unveil the role of bisphenol molecules – compounds that share a striking resemblance to oestrogens and can potentially wield influence over hormonal regulation and estrogen receptor activity. ??

These bisphenols could potentially cast their shadow on critical processes like oocyte maturation, spermatogenesis, and even the development of the reproductive system itself. An in-depth review from 2019 delves into the matter, specifically highlighting bisphenol S (BPS), which has replaced BPA in many products. It suggests that BPS might just have a similar negative impact on reproduction, potentially leading to fertility issues. ??

Surprisingly, BPS has been marketed as an industrial alternative to the notorious endocrine disruptor, BPA. You might even find it in products boasting the "BPA-free" label. This shift has prompted concern as both BPS and its cousin bisphenol F (BPF) have made their way into our lives. Data from NHANES 2013-2014 paints a vivid picture – BPA, BPS, and BPF were detected in 95.7%, 89.4%, and 66.5% of randomly selected urine samples, hinting that our exposure to these compounds might be more widespread than we imagined. ??

In the realm of human health, intriguing associations have emerged. High urinary BPA levels seem to correspond with increased serum levels of hormones like testosterone, oestradiol, and pregnenolone in girls facing early puberty. It's noteworthy that estrogen metabolism and BPA levels appear linked, although the relationship doesn't automatically imply causation. Similar connections have been observed between BPA and conditions like polycystic ovarian syndrome (PCOS) and ovarian failure. This poses some compelling questions about the role of these compounds in our reproductive well-being. ??

Non-human animals haven't been spared from the effects of bisphenols either. BPA has shown its ability to disrupt the Hypothalamus-Pituitary-Gonad (HPG) axis in species ranging from mice and rats to zebrafish. In the aquatic world, a study with C. riparius midges showcases a fascinating twist. After just a 24-hour exposure to BPS, these tiny larvae displayed altered transcription profiles in genes involved in the endocrine and biotransformation pathways. The findings hint at BPS potentially acting as a hormone agonist, triggering a cascade of molecular responses. ??

This journey through the realm of bisphenols and their impact on reproductive health underscores the complex interplay between chemicals and our bodies. 

Reference
Chang CJ, O’Brien KM, Keil AP, et al. Use of straighteners and other hair products and incident uterine cancer. J Natl Cancer Inst. 2022;114(12):1636-1645. doi:10.1093/jnci/djac165
Piazza MJ, Urbanetz AA. Environmental toxins and the impact of other endocrine disrupting chemicals in women’s reproductive health. JBRA Assist Reprod. 2019;23(2):154-164. doi:10.5935/1518-0557.20190016
Lauretta R, Sansone A, Sansone M, Romanelli F, Appetecchia M. Endocrine disrupting chemicals: effects on endocrine glands. Front Endocrinol (Lausanne). 2019;10:178. doi:10.3389/fendo.2019.00178
Peinado FM, Iribarne-Durán LM, Ocón-Hernández O, Olea N, Artacho-Cordón F. Endocrine disrupting chemicals in cosmetics and personal care products and risk of endometriosis. IntechOpen. Published online June 29, 2020. doi:10.5772/intechopen.93091
Millennial women key to growth in cosmetics industry. Tabs Analytics. Published January 20, 2016. Accessed August 2, 2023. https://www.tabsanalytics.com/blog/millennial-women-key-to-growth-in-cosmetics-industry
Di Renzo GC, Conry JA, Blake J, et al. International Federation of Gynecology and Obstetrics opinion on reproductive health impacts of exposure to toxic environmental chemicals. Int J Gynaecol Obstet. 2015;131(3):219-225. doi:10.1016/j.ijgo.2015.09.002
Buttke DE, Sircar K, Martin C. Exposures to endocrine-disrupting chemicals and age of menarche in adolescent girls in NHANES (2003-2008). Environ Health Perspect. 2012;120(11):1613-1618. doi:10.1289/ehp.1104748
Grindler NM, Allsworth JE, Macones GA, Kannan K, Roehl KA, Cooper AR. Persistent organic pollutants and early menopause in U.S. women. PLoS One. 2015;10(1):E116057. doi:10.1371/journal.pone.0116057
Kawa IA, Akbar masood, Fatima Q, et al. Endocrine disrupting chemical bisphenol A and its potential effects on female health. Diabetes Metab Syndr. 2021;15(3):803-811. doi:10.1016/j.dsx.2021.03.031
 Centers for Disease Control and Disease Prevention. Fourth national report on human exposure to environmental chemicals. Published February 2015. Accessed August 2, 2023. https://www.cdc.gov/biomonitoring/pdf/fourthreport_updatedtables_feb2015.pdf
 Mikolajewska K, Stragierowicz J, Gromadzinska J. Bisphenol A – application, sources of exposure and potential risks in infants, children and pregnant women. Int J Occup Med Environ Health. 2015;28(2):209-241. doi:10.13075/ijomeh.1896.00343
 Gonsioroski A, Mourikes VE, Flaws JA. Endocrine disruptors in water and their effects on the reproductive system. Int J Mol Sci. 2020;21(6):1929. doi:10.3390/ijms21061929
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 Lehmler HJ, Liu B, Gadogbe M, Bao W. Exposure to bisphenol A, bisphenol F, and bisphenol S in U.S. adults and children: the National Health and Nutrition Examination Survey 2013–2014. ACS Omega. 2018;3(6):6523-6532. doi:10.1021/acsomega.8b00824
 Lee S, Kang S, Choi M, et al. Changes in steroid metabolism among girls with precocious puberty may not be associated with urinary levels of bisphenol A. Reprod Toxicol. 2014;44:1-6. doi:10.1016/j.reprotox.2013.03.008

 

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