Skip to main content
. Author manuscript; available in PMC: 2020 Nov 1.
Published in final edited form as: Environ Res. 2019 Sep 8;178:108729. doi: 10.1016/j.envres.2019.108729

Table 2.

The associations of each phthalate metabolite or antioxidant with HOMA-IR among 1,605 participants based on the multiple linear regression model.

Urinary phthalate metabolites β (95%CI) P-value
MBzP1 0.018 (−0.013, 0.049) 0.26
MBP1 0.058 (0.021, 0.094) <.01
MiBP1 0.058 (0.023, 0.092) <.01
MEP1 −0.024 (−0.048, 0.001) 0.06
MCPP1 0.043 (0.009, 0.077) 0.01
ΣDEHP1 0.055 (0.027, 0.083) <.001
Vitamin A2 0.215 (0.090, 0.339) <.001
Vitamin C2 −0.053 (−0.103, −0.003) 0.04
Vitamin E2 −0.002 (−0.100, 0.096) 0.97
α–carotene2 −0.110 (−0.149, −0.070) <.0001
β-carotene2 −0.179 (−0.226, −0.132) <.0001
β-cryptoxanthin2 −0.117 (−0.170, −0.064) <.0001
Lycopene2 −0.053 (−0.119, 0.012) 0.11
Lutein/zeaxanthin2 −0.139 (−0.215, −0.063) <.001
*

All models were adjusted for age, gender, BMI, race, education level, physical activity, serum cotinine, urinary creatinine, and poverty-income ratio.

Urinary phthalate, serum antioxidants, and HOMA-IR were log transformed.

1

β represents the one unit change in log HOMA-IR per one unit increase in log urinary concentrations of the phthalate.

2

β represents the one unit change in HOMA-IR per one unit increase in log urinary concentrations of the antioxidant.