Plasma homocysteine level, estradiol level, and brain atrophy: a Mendelian randomization study

Author:

Gao Wen1,Zhu Wei-Wen2,Yu Ya-Huan1,Wang Juan1

Affiliation:

1. Guangzhou Medical University Department of Epidemiology and Health Statistics, School of Public Health, , Guangzhou 511436, China

2. The Second Affiliated Hospital of Guangzhou Medical University Department of Neurology, , Guangzhou 510260, China

Abstract

Abstract Objectives Observational studies link elevated plasma homocysteine (Hcy) with vascular disease. Our aim was to assess the gender difference in the association between the plasma tHcy level and brain atrophy and identify the possible influencer. We employed Mendelian randomization (MR) to explore the causal relationship between plasma tHcy level, estradiol level, and brain atrophy. Methods A total of 687 patients with brain atrophy were included, and gender-specific subgroup analyses in association between tHcy and brain atrophy are conducted. From genome-wide association studies, we selected genetic variants (P < 5 × 10−8) for the plasma tHcy level and estradiol level. We investigated the degree of brain atrophy (including gray matter volume and total brain volume) in the UK biobank (n = 7,916). The inverse variance–weighted and several sensitivity MR regression analyses were carried out. Results The plasma tHcy level was significantly associated with brain atrophy for females, but not for males. An MR study showed that there was little evidence of the causal link between elevated plasma tHcy and brain atrophy. On the other hand, we found evidence to support causality for genetically decreased estradiol with higher risk of brain atrophy. Furthermore, genetic predisposition to elevated plasma tHcy was associated with a lower estradiol level. Conclusions The influence of estradiol on the association between tHcy and brain atrophy deserves further investigation.

Funder

National Natural Science Fund project

Guangdong Provincial Natural Science Fund project

Publisher

Oxford University Press (OUP)

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