Frontiers in Genetics (Oct 2021)
Exome-Wide Association Study Identifies East Asian-Specific Missense Variant MTHFR C136T Influencing Homocysteine Levels in Chinese Populations RH: ExWAS of tHCY in a Chinese Population
- Tianzi Liu,
- Tianzi Liu,
- Mohetaboer Momin,
- Mohetaboer Momin,
- Huiyue Zhou,
- Huiyue Zhou,
- Qiwen Zheng,
- Qiwen Zheng,
- Fangfang Fan,
- Fangfang Fan,
- Jia Jia,
- Jia Jia,
- Mengyuan Liu,
- Mengyuan Liu,
- Minghui Bao,
- Minghui Bao,
- Jianping Li,
- Jianping Li,
- Yong Huo,
- Yong Huo,
- Jialin Liu,
- Jialin Liu,
- Jialin Liu,
- Yaning Zhang,
- Yaning Zhang,
- Yaning Zhang,
- Xuemei Mao,
- Xiao Han,
- Zhiyuan Hu,
- Zhiyuan Hu,
- Zhiyuan Hu,
- Changqing Zeng,
- Changqing Zeng,
- Changqing Zeng,
- Fan Liu,
- Fan Liu,
- Fan Liu,
- Yan Zhang,
- Yan Zhang
Affiliations
- Tianzi Liu
- CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China
- Tianzi Liu
- China National Center for Bioinformation, Beijing, China
- Mohetaboer Momin
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Mohetaboer Momin
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- Huiyue Zhou
- CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China
- Huiyue Zhou
- China National Center for Bioinformation, Beijing, China
- Qiwen Zheng
- CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China
- Qiwen Zheng
- China National Center for Bioinformation, Beijing, China
- Fangfang Fan
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Fangfang Fan
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- Jia Jia
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Jia Jia
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- Mengyuan Liu
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Mengyuan Liu
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- Minghui Bao
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Minghui Bao
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- Jianping Li
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Jianping Li
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- Yong Huo
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Yong Huo
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- Jialin Liu
- CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China
- Jialin Liu
- China National Center for Bioinformation, Beijing, China
- Jialin Liu
- University of Chinese Academy of Sciences, Beijing, China
- Yaning Zhang
- CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China
- Yaning Zhang
- China National Center for Bioinformation, Beijing, China
- Yaning Zhang
- University of Chinese Academy of Sciences, Beijing, China
- Xuemei Mao
- Beijing P4 Healthcare Institute, Beijing, China
- Xiao Han
- Beijing P4 Healthcare Institute, Beijing, China
- Zhiyuan Hu
- Beijing P4 Healthcare Institute, Beijing, China
- Zhiyuan Hu
- CAS Key Laboratory of Standardization and Measurement for Nanotechnology, CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, Beijing, China
- Zhiyuan Hu
- School of Nanoscience and Technology, Sino-Danish College, University of Chinese Academy of Sciences, Beijing, China
- Changqing Zeng
- CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China
- Changqing Zeng
- China National Center for Bioinformation, Beijing, China
- Changqing Zeng
- University of Chinese Academy of Sciences, Beijing, China
- Fan Liu
- CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China
- Fan Liu
- China National Center for Bioinformation, Beijing, China
- Fan Liu
- University of Chinese Academy of Sciences, Beijing, China
- Yan Zhang
- Department of Cardiology, Peking University First Hospital, Beijing, China
- Yan Zhang
- Institute of Cardiovascular Disease, Peking University First Hospital, Beijing, China
- DOI
- https://doi.org/10.3389/fgene.2021.717621
- Journal volume & issue
-
Vol. 12
Abstract
Plasma total homocysteine (tHCY) is a known risk factor of a wide range of complex diseases. No genome scans for tHCY have been conducted in East Asian populations. Here, we conducted an exome-wide association study (ExWAS) for tHCY in 5,175 individuals of Chinese Han origin, followed by a replication study in 668 Chinese individuals. The ExWAS identified two loci, 1p36.22 (lead single-nucleotide polymorphism (SNP) rs1801133, MTHFR C677T) and 16q24.3 (rs1126464, DPEP1), showing exome-wide significant association with tHCY (p < 5E−7); and both loci have been previously associated with tHCY in non-East Asian populations. Both SNPs were replicated in the replication study (p < 0.05). Conditioning on the genotype of C677T and rs1126464, we identified a novel East Asian-specific missense variant rs138189536 (C136T) of MTHFR (p = 6.53E−10), which was also significant in the replication study (p = 9.8E−3). The C136T and C677T variants affect tHCY in a compound heterozygote manner, where compound heterozygote and homozygote genotype carriers had on average 43.4% increased tHCY than had other genotypes. The frequency of the homozygote C677T genotype showed an inverse-U-shaped geospatial pattern globally with a pronounced frequency in northern China, which coincided with the high prevalence of hyperhomocysteinemia (HHCY) in northern China. A logistic regression model of HHCY status considering sex, age, and the genotypes of the three identified variants reached an area under the receiver operating characteristic curve (AUC) value of 0.74 in an independent validation cohort. These genetic observations provide new insights into the presence of multiple causal mutations at the MTHFR locus, highlight the role of genetics in HHCY epidemiology among different populations, and provide candidate loci for future functional studies.
Keywords