Kaio Cezar Rodrigues Salum, Izadora Sthephanie da Silva Assis, Úrsula de Almeida Kopke, Lohanna Palhinha, Gabriella de Medeiros Abreu, Laura Wendling Gouvêa, Myrela Ribeiro Teixeira, Fernanda Cristina C Mattos, José Firmino Nogueira Neto, Rafaela de Freitas Martins Felício, Eliane Lopes Rosado, Verônica Marques Zembrzuski, Mario Campos Junior, Clarissa Menezes Maya-Monteiro, Pedro Hernán Cabello, João Regis Ivar Carneiro, Patrícia Torres Bozza, Fabiana Barzotto Kohlrausch, Ana Carolina Proença da Fonseca
{"title":"FTO rs17817449变异增加巴西队列中严重肥胖的风险:一项病例对照研究","authors":"Kaio Cezar Rodrigues Salum, Izadora Sthephanie da Silva Assis, Úrsula de Almeida Kopke, Lohanna Palhinha, Gabriella de Medeiros Abreu, Laura Wendling Gouvêa, Myrela Ribeiro Teixeira, Fernanda Cristina C Mattos, José Firmino Nogueira Neto, Rafaela de Freitas Martins Felício, Eliane Lopes Rosado, Verônica Marques Zembrzuski, Mario Campos Junior, Clarissa Menezes Maya-Monteiro, Pedro Hernán Cabello, João Regis Ivar Carneiro, Patrícia Torres Bozza, Fabiana Barzotto Kohlrausch, Ana Carolina Proença da Fonseca","doi":"10.2147/DMSO.S451401","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Obesity is a complex disease caused by a combination of genetic, environmental, and epigenetic factors, and is associated with an increased risk of chronic diseases. The leptin-melanocortin pathway integrates peripheral signals about the body's energy stores with a central neuronal circuit in the hypothalamus. This pathway has been extensively studied over the years, as genetic variations in genes related to it may play a crucial role in determining an individual's susceptibility to obesity. Therefore, we analyzed the association between obesity and specific polymorphisms in leptin-melanocortin-related genes such as <i>LEPR</i> rs1137101, <i>POMC</i> rs1042571, <i>LEP</i> rs7799039, <i>BDNF</i> rs6265, <i>FTO</i> rs17817449, <i>CART</i> rs121909065, and <i>NPY</i> rs16147/rs5574.</p><p><strong>Patients and methods: </strong>The study enrolled 501 participants from Rio de Janeiro, Brazil, with obesity class II or greater (BMI ≥ 35 kg/m2) and normal weight controls (18.5≤ BMI ≤24.9 kg/m2). We collected demographic, body composition, biochemical, and genotyping data by real-time PCR, and performed logistic and linear regression analyses to investigate the association of polymorphisms with severe obesity status and obesity-related quantitative parameters.</p><p><strong>Results: </strong>Individuals with severe obesity had significantly higher anthropometric measures, blood pressure, and biochemical levels. The <i>FTO</i> rs17817449 TT genotype was associated with a significantly higher risk of developing severe obesity, and distinct cytokine expression was observed across the <i>FTO</i> rs17817449 genotypes. The <i>BDNF</i> rs6265 dominant-model and <i>NPY</i> rs16147 CC genotypes were associated with triglyceride levels and childhood obesity, respectively. Finally, individuals with obesity were more likely to carry a greater number of risk alleles than those without obesity.</p><p><strong>Conclusion: </strong>Our study observed an important association between <i>FTO</i> rs17817449 polymorphism with obesity and obesity-related traits. Additionally, <i>BDNF</i> rs6265 dominant-model was associated with triglyceride serum levels, and <i>NPY</i> rs16147 may have a role in obesity onset.</p>","PeriodicalId":11116,"journal":{"name":"Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy","volume":"18 ","pages":"283-303"},"PeriodicalIF":2.8000,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11792641/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>FTO</i> rs17817449 Variant Increases the Risk of Severe Obesity in a Brazilian Cohort: A Case-Control Study.\",\"authors\":\"Kaio Cezar Rodrigues Salum, Izadora Sthephanie da Silva Assis, Úrsula de Almeida Kopke, Lohanna Palhinha, Gabriella de Medeiros Abreu, Laura Wendling Gouvêa, Myrela Ribeiro Teixeira, Fernanda Cristina C Mattos, José Firmino Nogueira Neto, Rafaela de Freitas Martins Felício, Eliane Lopes Rosado, Verônica Marques Zembrzuski, Mario Campos Junior, Clarissa Menezes Maya-Monteiro, Pedro Hernán Cabello, João Regis Ivar Carneiro, Patrícia Torres Bozza, Fabiana Barzotto Kohlrausch, Ana Carolina Proença da Fonseca\",\"doi\":\"10.2147/DMSO.S451401\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Obesity is a complex disease caused by a combination of genetic, environmental, and epigenetic factors, and is associated with an increased risk of chronic diseases. The leptin-melanocortin pathway integrates peripheral signals about the body's energy stores with a central neuronal circuit in the hypothalamus. This pathway has been extensively studied over the years, as genetic variations in genes related to it may play a crucial role in determining an individual's susceptibility to obesity. Therefore, we analyzed the association between obesity and specific polymorphisms in leptin-melanocortin-related genes such as <i>LEPR</i> rs1137101, <i>POMC</i> rs1042571, <i>LEP</i> rs7799039, <i>BDNF</i> rs6265, <i>FTO</i> rs17817449, <i>CART</i> rs121909065, and <i>NPY</i> rs16147/rs5574.</p><p><strong>Patients and methods: </strong>The study enrolled 501 participants from Rio de Janeiro, Brazil, with obesity class II or greater (BMI ≥ 35 kg/m2) and normal weight controls (18.5≤ BMI ≤24.9 kg/m2). We collected demographic, body composition, biochemical, and genotyping data by real-time PCR, and performed logistic and linear regression analyses to investigate the association of polymorphisms with severe obesity status and obesity-related quantitative parameters.</p><p><strong>Results: </strong>Individuals with severe obesity had significantly higher anthropometric measures, blood pressure, and biochemical levels. The <i>FTO</i> rs17817449 TT genotype was associated with a significantly higher risk of developing severe obesity, and distinct cytokine expression was observed across the <i>FTO</i> rs17817449 genotypes. The <i>BDNF</i> rs6265 dominant-model and <i>NPY</i> rs16147 CC genotypes were associated with triglyceride levels and childhood obesity, respectively. Finally, individuals with obesity were more likely to carry a greater number of risk alleles than those without obesity.</p><p><strong>Conclusion: </strong>Our study observed an important association between <i>FTO</i> rs17817449 polymorphism with obesity and obesity-related traits. Additionally, <i>BDNF</i> rs6265 dominant-model was associated with triglyceride serum levels, and <i>NPY</i> rs16147 may have a role in obesity onset.</p>\",\"PeriodicalId\":11116,\"journal\":{\"name\":\"Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy\",\"volume\":\"18 \",\"pages\":\"283-303\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-01-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11792641/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2147/DMSO.S451401\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/DMSO.S451401","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
FTO rs17817449 Variant Increases the Risk of Severe Obesity in a Brazilian Cohort: A Case-Control Study.
Purpose: Obesity is a complex disease caused by a combination of genetic, environmental, and epigenetic factors, and is associated with an increased risk of chronic diseases. The leptin-melanocortin pathway integrates peripheral signals about the body's energy stores with a central neuronal circuit in the hypothalamus. This pathway has been extensively studied over the years, as genetic variations in genes related to it may play a crucial role in determining an individual's susceptibility to obesity. Therefore, we analyzed the association between obesity and specific polymorphisms in leptin-melanocortin-related genes such as LEPR rs1137101, POMC rs1042571, LEP rs7799039, BDNF rs6265, FTO rs17817449, CART rs121909065, and NPY rs16147/rs5574.
Patients and methods: The study enrolled 501 participants from Rio de Janeiro, Brazil, with obesity class II or greater (BMI ≥ 35 kg/m2) and normal weight controls (18.5≤ BMI ≤24.9 kg/m2). We collected demographic, body composition, biochemical, and genotyping data by real-time PCR, and performed logistic and linear regression analyses to investigate the association of polymorphisms with severe obesity status and obesity-related quantitative parameters.
Results: Individuals with severe obesity had significantly higher anthropometric measures, blood pressure, and biochemical levels. The FTO rs17817449 TT genotype was associated with a significantly higher risk of developing severe obesity, and distinct cytokine expression was observed across the FTO rs17817449 genotypes. The BDNF rs6265 dominant-model and NPY rs16147 CC genotypes were associated with triglyceride levels and childhood obesity, respectively. Finally, individuals with obesity were more likely to carry a greater number of risk alleles than those without obesity.
Conclusion: Our study observed an important association between FTO rs17817449 polymorphism with obesity and obesity-related traits. Additionally, BDNF rs6265 dominant-model was associated with triglyceride serum levels, and NPY rs16147 may have a role in obesity onset.
期刊介绍:
An international, peer-reviewed, open access, online journal. The journal is committed to the rapid publication of the latest laboratory and clinical findings in the fields of diabetes, metabolic syndrome and obesity research. Original research, review, case reports, hypothesis formation, expert opinion and commentaries are all considered for publication.