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. 2019 Apr 11;17(1):77.
doi: 10.1186/s12916-019-1309-6.

Exploring telomere length in mother-newborn pairs in relation to exposure to multiple toxic metals and potential modifying effects by nutritional factors

Affiliations

Exploring telomere length in mother-newborn pairs in relation to exposure to multiple toxic metals and potential modifying effects by nutritional factors

Maria Herlin et al. BMC Med. .

Abstract

Background: The uterine environment may influence telomere length at birth, which is essential for cellular function, aging, and disease susceptibility over the lifespan. However, little is known about the impact of toxic chemicals on early-life telomeres. Therefore, we assessed the potential impact of multiple toxic metals on relative telomere length (rTL) in the maternal blood, cord blood, and placenta, as well as the potential modifying effects of pro-oxidants.

Method: In a mother-child cohort in northern Argentina (n = 169), we measured multiple toxic metals in the maternal blood or urine collected during late pregnancy, as well as the placenta and cord blood collected at delivery, using inductively coupled plasma mass spectrometry (ICP-MS). We assessed associations of log2-transformed metal concentrations with rTL, measured in maternal and cord blood leukocytes and the placenta by real-time PCR, using multivariable-adjusted linear regression. Additionally, we tested for modifications by antioxidants (zinc, selenium, folate, and vitamin D3).

Results: Exposure to boron and antimony during pregnancy was associated with shorter maternal rTL, and lithium with longer maternal rTL; a doubling of exposure was associated with changes corresponding to 0.2-0.4 standard deviations (SD) of the rTL. Arsenic concentrations in the placenta (n = 98), blood, and urine were positively associated with placental rTL, about 0.2 SD by doubled arsenic. In the cord blood (n = 88), only lead was associated with rTL (inversely), particularly in boys (p for interaction 0.09). Stratifying by newborn sex showed ten times stronger association in boys (about 0.6 SD) than in girls. The studied antioxidants did not modify the associations, except that with antimony.

Conclusions: Elevated exposure to boron, lithium, arsenic, and antimony was associated with maternal or newborn rTL in a tissue-specific, for lead also sex-specific, manner. Nutritional antioxidants did not generally influence the associations.

Keywords: Antimony; Arsenic; Boron; Early life programming; Lead; Lithium; Nutrients; Telomeres; Zinc.

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Conflict of interest statement

Ethics approval and consent to participate

The study was performed in accordance with the Declaration of Helsinki and approved by the Ministry of Health, Salta, Argentina, and the regional ethical committee at Karolinska Institutet, Stockholm, Sweden (2012/2:7). Prior to recruitment, written informed consent was obtained from all women after oral and written explanation of study details. For the few women under 18 years of age, informed consent was also obtained from the caregiver. As the drinking water was a main source of the toxic exposures, we communicated the water contaminant concentrations to the hospital and the Health Ministry in Salta. Women were referred to the hospital doctors whenever any medical problems were observed.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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References

    1. Blackburn EH. Telomeres and telomerase: their mechanisms of action and the effects of altering their functions. FEBS Lett. 2005;579(4):859–862. doi: 10.1016/j.febslet.2004.11.036. - DOI - PubMed
    1. O’Sullivan RJ, Karlseder J. Telomeres: protecting chromosomes against genome instability. Nat Rev Mol Cell Biol. 2010;11(3):171–181. doi: 10.1038/nrm2848. - DOI - PMC - PubMed
    1. Blackburn EH, Epel ES, Lin J. Human telomere biology: a contributory and interactive factor in aging, disease risks, and protection. Science. 2015;350(6265):1193–1198. doi: 10.1126/science.aab3389. - DOI - PubMed
    1. Fragkiadaki P, Tsoukalas D, Fragkiadoulaki I, Psycharakis C, Nikitovic D, Spandidos DA, et al. Telomerase activity in pregnancy complications (review) Mol Med Rep. 2016;14(1):16–21. doi: 10.3892/mmr.2016.5231. - DOI - PMC - PubMed
    1. Entringer Sonja, de Punder Karin, Buss Claudia, Wadhwa Pathik D. The fetal programming of telomere biology hypothesis: an update. Philosophical Transactions of the Royal Society B: Biological Sciences. 2018;373(1741):20170151. doi: 10.1098/rstb.2017.0151. - DOI - PMC - PubMed

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