Shilna Azhuvalappil , Raghav Prasad , Pravin Sahadevan , Hitesh Pradhan , Pooja Rai , Jonas S. Sundarakumar
{"title":"中老年农村印第安人 APOE 基因型与代谢综合征之间的性别差异","authors":"Shilna Azhuvalappil , Raghav Prasad , Pravin Sahadevan , Hitesh Pradhan , Pooja Rai , Jonas S. Sundarakumar","doi":"10.1016/j.metop.2024.100281","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Metabolic syndrome (MetS), characterized by elevated blood pressure, high blood glucose, excess abdominal fat, and abnormal cholesterol or triglyceride levels, significantly increases the risk of various non-communicable diseases. This study focuses on understanding the sex-specific association between Apolipoprotein E (APOE) polymorphism and MetS among middle-aged and older adults in rural southern India.</p></div><div><h3>Methods</h3><p>This cross-sectional study utilized data from the Centre for Brain Research-Srinivaspura Aging, Neuro Senescence, and COGnition (CBR-SANSCOG) study. Participants (n = 3741) underwent comprehensive clinical assessments and blood investigations, including APOE genotyping. MetS was defined using the National Cholesterol Education Program – Adult Treatment Panel III (NCEP ATP III) and the Consensus criteria. Statistical analyses, including chi-square tests, ANCOVA, and logistic regression, were conducted to explore the association of APOE genotype with MetS and its components, stratified by sex.</p></div><div><h3>Results</h3><p>Females carrying the APOE E4 allele had 1.31-fold increased odds of MetS (95 % CI: 1.02,1.69, p = 0.035) according to the NCEP ATP III criteria but not when the Consensus criteria were applied. The study also noted sex-specific differences in the association of APOE with various MetS components, including lipid levels and waist circumference.</p></div><div><h3>Discussion</h3><p>Our findings reveal a sex-specific association between the APOE E4 allele and MetS, with only females having an increased risk. This study contributes to the understanding of the genetic underpinnings of MetS and highlights the importance of considering sex-specific differences in MetS research and its prevention strategies. This study underscores the complexity of MetS etiology and emphasizes the need for further research to elucidate the role of genetic, environmental, and lifestyle factors in its progression, particularly in sex-specific contexts.</p></div>","PeriodicalId":94141,"journal":{"name":"Metabolism open","volume":"22 ","pages":"Article 100281"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2589936824000136/pdfft?md5=8050e46bec5a44c2dbb105c5e875656c&pid=1-s2.0-S2589936824000136-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Sex-specific differences in the association between APOE genotype and metabolic syndrome among middle-aged and older rural Indians\",\"authors\":\"Shilna Azhuvalappil , Raghav Prasad , Pravin Sahadevan , Hitesh Pradhan , Pooja Rai , Jonas S. Sundarakumar\",\"doi\":\"10.1016/j.metop.2024.100281\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Metabolic syndrome (MetS), characterized by elevated blood pressure, high blood glucose, excess abdominal fat, and abnormal cholesterol or triglyceride levels, significantly increases the risk of various non-communicable diseases. This study focuses on understanding the sex-specific association between Apolipoprotein E (APOE) polymorphism and MetS among middle-aged and older adults in rural southern India.</p></div><div><h3>Methods</h3><p>This cross-sectional study utilized data from the Centre for Brain Research-Srinivaspura Aging, Neuro Senescence, and COGnition (CBR-SANSCOG) study. Participants (n = 3741) underwent comprehensive clinical assessments and blood investigations, including APOE genotyping. MetS was defined using the National Cholesterol Education Program – Adult Treatment Panel III (NCEP ATP III) and the Consensus criteria. Statistical analyses, including chi-square tests, ANCOVA, and logistic regression, were conducted to explore the association of APOE genotype with MetS and its components, stratified by sex.</p></div><div><h3>Results</h3><p>Females carrying the APOE E4 allele had 1.31-fold increased odds of MetS (95 % CI: 1.02,1.69, p = 0.035) according to the NCEP ATP III criteria but not when the Consensus criteria were applied. The study also noted sex-specific differences in the association of APOE with various MetS components, including lipid levels and waist circumference.</p></div><div><h3>Discussion</h3><p>Our findings reveal a sex-specific association between the APOE E4 allele and MetS, with only females having an increased risk. This study contributes to the understanding of the genetic underpinnings of MetS and highlights the importance of considering sex-specific differences in MetS research and its prevention strategies. This study underscores the complexity of MetS etiology and emphasizes the need for further research to elucidate the role of genetic, environmental, and lifestyle factors in its progression, particularly in sex-specific contexts.</p></div>\",\"PeriodicalId\":94141,\"journal\":{\"name\":\"Metabolism open\",\"volume\":\"22 \",\"pages\":\"Article 100281\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2589936824000136/pdfft?md5=8050e46bec5a44c2dbb105c5e875656c&pid=1-s2.0-S2589936824000136-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Metabolism open\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2589936824000136\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Metabolism open","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589936824000136","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景以血压升高、高血糖、腹部脂肪过多、胆固醇或甘油三酯水平异常为特征的代谢综合征(MetS)会显著增加罹患各种非传染性疾病的风险。这项研究的重点是了解印度南部农村地区中老年人载脂蛋白 E(APOE)多态性与 MetS 之间的性别特异性关联。方法这项横断面研究利用了脑研究中心-斯里尼瓦斯普拉老龄化、神经衰老和 COGnition(CBR-SANSCOG)研究的数据。参与者(n = 3741)接受了全面的临床评估和血液检查,包括 APOE 基因分型。MetS 采用美国国家胆固醇教育计划-成人治疗小组 III(NCEP ATP III)和共识标准进行定义。结果根据 NCEP ATP III 标准,携带 APOE E4 等位基因的女性患 MetS 的几率增加了 1.31 倍(95 % CI:1.02,1.69, p = 0.035),但如果采用共识标准,则没有增加。该研究还注意到 APOE 与 MetS 的各种成分(包括血脂水平和腰围)之间存在性别特异性差异。这项研究有助于人们了解 MetS 的遗传基础,并强调了在 MetS 研究及其预防策略中考虑性别差异的重要性。这项研究强调了 MetS 病因学的复杂性,并强调有必要开展进一步研究,以阐明遗传、环境和生活方式因素在其发展过程中的作用,尤其是在特定性别背景下的作用。
Sex-specific differences in the association between APOE genotype and metabolic syndrome among middle-aged and older rural Indians
Background
Metabolic syndrome (MetS), characterized by elevated blood pressure, high blood glucose, excess abdominal fat, and abnormal cholesterol or triglyceride levels, significantly increases the risk of various non-communicable diseases. This study focuses on understanding the sex-specific association between Apolipoprotein E (APOE) polymorphism and MetS among middle-aged and older adults in rural southern India.
Methods
This cross-sectional study utilized data from the Centre for Brain Research-Srinivaspura Aging, Neuro Senescence, and COGnition (CBR-SANSCOG) study. Participants (n = 3741) underwent comprehensive clinical assessments and blood investigations, including APOE genotyping. MetS was defined using the National Cholesterol Education Program – Adult Treatment Panel III (NCEP ATP III) and the Consensus criteria. Statistical analyses, including chi-square tests, ANCOVA, and logistic regression, were conducted to explore the association of APOE genotype with MetS and its components, stratified by sex.
Results
Females carrying the APOE E4 allele had 1.31-fold increased odds of MetS (95 % CI: 1.02,1.69, p = 0.035) according to the NCEP ATP III criteria but not when the Consensus criteria were applied. The study also noted sex-specific differences in the association of APOE with various MetS components, including lipid levels and waist circumference.
Discussion
Our findings reveal a sex-specific association between the APOE E4 allele and MetS, with only females having an increased risk. This study contributes to the understanding of the genetic underpinnings of MetS and highlights the importance of considering sex-specific differences in MetS research and its prevention strategies. This study underscores the complexity of MetS etiology and emphasizes the need for further research to elucidate the role of genetic, environmental, and lifestyle factors in its progression, particularly in sex-specific contexts.