Genotype-environment interaction on arterial stiffness: A pedigree-based study.
- Author:
Xue Heng WANG
1
;
Si Yue WANG
1
;
He Xiang PENG
1
;
Meng FAN
1
;
Huang Da GUO
1
;
Tian Jiao HOU
1
;
Meng Ying WANG
1
;
Yi Qun WU
1
;
Xue Ying QIN
1
;
Xun TANG
1
;
Jin LI
1
;
Da Fang CHEN
1
;
Yong Hua HU
1
;
Tao WU
1
Author Information
1. Department of Epidemiology and Biostatistics, Peking University School of Public Health, Beijing 100191, China.
- Publication Type:Journal Article
- Keywords:
Arterial stiffness;
Gene-environment interaction;
Lifestyle;
Pedigree
- MeSH:
Humans;
Male;
Middle Aged;
Female;
Ankle Brachial Index;
Cohort Studies;
Gene-Environment Interaction;
Vascular Stiffness/genetics*;
Pedigree;
Pulse Wave Analysis/methods*;
Genotype
- From:
Journal of Peking University(Health Sciences)
2023;55(3):400-407
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To utilized the baseline data of the Beijing Fangshan Family Cohort Study, and to estimate whether the association between a healthy lifestyle and arterial stiffness might be modified by genetic effects.
METHODS:Probands and their relatives from 9 rural areas in Fangshan district, Beijing were included in this study. We developed a healthy lifestyle score based on five lifestyle behaviors: smoking, alcohol consumption, body mass index (BMI), dietary pattern, and physical activity. The measurements of arterial stiffness were brachial-ankle pulse wave velocity (baPWV) and ankle-brachial index (ABI). A variance component model was used to determine the heritability of arterial stiffness. Genotype-environment interaction effects were performed by the maximum likelihood methods. Subsequently, 45 candidate single nucleotide polymorphisms (SNPs) located in the glycolipid metabolism pathway were selected, and generalized estimated equations were used to assess the gene-environment interaction effects between particular genetic loci and healthy lifestyles.
RESULTS:A total of 6 302 study subjects across 3 225 pedigrees were enrolled in this study, with a mean age of 56.9 years and 45.1% male. Heritability of baPWV and ABI was 0.360 (95%CI: 0.302-0.418) and 0.243 (95%CI: 0.175-0.311), respectively. Significant genotype-healthy diet interaction on baPWV and genotype-BMI interaction on ABI were observed. Following the findings of genotype-environment interaction analysis, we further identified two SNPs located in ADAMTS9-AS2 and CDH13 might modify the association between healthy dietary pattern and arterial stiffness, indicating that adherence to a healthy dietary pattern might attenuate the genetic risk on arterial stiffness. Three SNPs in CDKAL1, ATP8B2 and SLC30A8 were shown to interact with BMI, implying that maintaining BMI within a healthy range might decrease the genetic risk of arterial stiffness.
CONCLUSION:The current study discovered that genotype-healthy dietary pattern and genotype-BMI interactions might affect the risk of arterial stiffness. Furthermore, we identified five genetic loci that might modify the relationship between healthy dietary pattern and BMI with arterial stiffness. Our findings suggested that a healthy lifestyle may reduce the genetic risk of arterial stiffness. This study has laid the groundwork for future research exploring mechanisms of arterial stiffness.
