4.4 Article

Associations between maternal mono-(2-ethylhexyl) phthalate levels, nuclear receptor gene polymorphisms, and fatty acid levels in pregnant Japanese women in the Hokkaido study

Journal

REPRODUCTIVE TOXICOLOGY
Volume 107, Issue -, Pages 22-32

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.reprotox.2021.11.003

Keywords

Mono-(2-ethylhexyl) phthalate; Pregnancy; Genotype; Peroxisome proliferator-activated receptor coactivator 1A; Liver X receptor beta; Fatty acid

Funding

  1. Japanese Ministry of Health, Labour, and Welfare, Health and Labour Sciences Research Grants [H29 Kagaku-Ippan-002]
  2. Japan Society for the Promotion of Sciences, the Ministry of Education, Culture, Sports, Science and Technology [15K15220, 18H03035, 18K17348, 19H01071, 19K22730, 20K10445, 2589300403, 26740028]
  3. Grants-in-Aid for Scientific Research [20K10445, 19H01071, 19K22730, 18K17348, 26740028, 15K15220, 18H03035] Funding Source: KAKEN

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This study investigated how the interaction between mono-(2-ethylhexyl) phthalate (MEHP) and maternal genotypes associated with nuclear receptors affect fatty acid levels during pregnancy. The results showed that the interaction between MEHP and maternal genotypes PPARGC1A (rs8192678) and LXRB (rs2303044) can decrease fatty acid levels in pregnant Japanese individuals.
We assessed how the interaction between mono-(2-ethylhexyl) phthalate (MEHP) in maternal sera and the maternal genotypes associated with nuclear receptors affect fatty acid levels in a prospective birth cohort study of pregnant Japanese individuals (n = 437) recruited in Sapporo between 2002 and 2005. We analyzed MEHP and fatty acids using gas chromatography-mass spectrometry. Thirteen single nucleotide polymorphisms of peroxisome proliferator-activated receptor (PPAR) alpha, PPAR gamma (PPARG), PPARG coactivator 1A (PPARGC1A), PPAR delta, constitutive androstane receptor, liver X receptor (LXR) alpha, and LXR beta (LXRB) were analyzed using real-time PCR. Multiple linear regression models were used to confirm the influence of log(10)-transformed MEHP levels and maternal genotypes on log(10)-transformed fatty acid levels. When the effects of the interaction between MEHP levels and the maternal PPARGC1A (rs8192678) genotype on oleic acid levels were evaluated, the estimated changes (95 % confidence intervals) in oleic acid levels against MEHP levels, maternal PPARGC1A (rs8192678)-GA/AA genotype, and the interaction between them showed a mean reduction of 0.200 (0.079, 0.322), mean reduction of 0.141 (0.000, 0.283), and mean increase of 0.145 (0.010, 0.281), respectively, after adjusting for the perfluorooctanesulfonate level. The effects of the interaction between MEHP levels and maternal LXRB (rs2303044) genotype on linoleic acid levels was also significant (p(int) = 0.010). In conclusion, the interaction between MEHP and the maternal genotypes PPARGC1A (rs8192678) and LXRB (rs2303044) decreased fatty acid levels. Further, the interaction between MEHP and PPARGC1A (rs8192678) may have a greater effect on fatty acid levels than the interaction between PFOS and PPARGC1A.

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