Yéssika Weyman-Vela, Ada A Sandoval-Carrillo, Jose M Salas-Pacheco, Fernando Guerrero-Romero, Alma Cristina Salas-Leal, Luis E Simental-Mendía
{"title":"表达:LEP、LEPR和ADIPOQ基因的甲基化水平及其与代谢健康肥胖的关系","authors":"Yéssika Weyman-Vela, Ada A Sandoval-Carrillo, Jose M Salas-Pacheco, Fernando Guerrero-Romero, Alma Cristina Salas-Leal, Luis E Simental-Mendía","doi":"10.1177/10815589251378182","DOIUrl":null,"url":null,"abstract":"<p><p>It has been reported that DNA methylation in the epigenetic profile of the genes <i>LEP</i> and <i>ADIPOQ</i> is associated with obesity. To the best of our knowledge, there are no previous reports assessing the methylation of the <i>LEP</i>, <i>LEPR</i>, and <i>ADIPOQ</i> genes in subjects with metabolically healthy obesity (MHO). Therefore, the aim of this study was to determine the association between methylation of the <i>LEP</i>, <i>LEPR</i>, and <i>ADIPOQ</i> genes with the MHO phenotype. Healthy men and women aged 20-55 years of age with a body mass index ≥30 kg/m<sup>2</sup> were enrolled in a case-control study. Exclusion criteria were pregnancy, alcohol intake, smoking, diabetes, hypertension, hepatic disease, cardiovascular disease, renal disease, thyroid disease, cancer, and/or any type of drug therapy. Individuals with MHO were allocated to the case group, while those with metabolically unhealthy obesity (MUO) were assigned to the control group. A total of 78 individuals were enrolled and allocated into the groups with MHO (n = 39) or MUO (n = 39). In the MHO group, the methylation percentage of the <i>LEP</i> gene was significantly higher than in the MUO group, while the <i>LEPR</i> and <i>ADIPOQ</i> genes did not show differences between the study groups. Finally, the methylation of the <i>LEP</i> gene (OR = 1.67; 95% confidence interval (CI): 1.29-2.16; <i>p</i> < 0.001), but not of <i>LEPR</i> (OR = 0.77; 95% CI: 0.45-1.32; <i>p</i> = 0.350) and <i>ADIPOQ</i> (OR = 1.01; 95% CI: 0.97-1.05; <i>p</i> = 0.411), presented a positive association with the MHO phenotype. In conclusion, the <i>LEP</i> gene hypermethylation is positively associated with the MHO phenotype. In addition, the <i>LEPR</i> gene overexpression was significantly associated with the MHO.</p>","PeriodicalId":520677,"journal":{"name":"Journal of investigative medicine : the official publication of the American Federation for Clinical Research","volume":" ","pages":"10815589251378182"},"PeriodicalIF":2.0000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Methylation levels of the <i>LEP, LEPR</i>, and <i>ADIPOQ</i> genes and their association with metabolically healthy obesity.\",\"authors\":\"Yéssika Weyman-Vela, Ada A Sandoval-Carrillo, Jose M Salas-Pacheco, Fernando Guerrero-Romero, Alma Cristina Salas-Leal, Luis E Simental-Mendía\",\"doi\":\"10.1177/10815589251378182\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>It has been reported that DNA methylation in the epigenetic profile of the genes <i>LEP</i> and <i>ADIPOQ</i> is associated with obesity. To the best of our knowledge, there are no previous reports assessing the methylation of the <i>LEP</i>, <i>LEPR</i>, and <i>ADIPOQ</i> genes in subjects with metabolically healthy obesity (MHO). Therefore, the aim of this study was to determine the association between methylation of the <i>LEP</i>, <i>LEPR</i>, and <i>ADIPOQ</i> genes with the MHO phenotype. Healthy men and women aged 20-55 years of age with a body mass index ≥30 kg/m<sup>2</sup> were enrolled in a case-control study. Exclusion criteria were pregnancy, alcohol intake, smoking, diabetes, hypertension, hepatic disease, cardiovascular disease, renal disease, thyroid disease, cancer, and/or any type of drug therapy. Individuals with MHO were allocated to the case group, while those with metabolically unhealthy obesity (MUO) were assigned to the control group. A total of 78 individuals were enrolled and allocated into the groups with MHO (n = 39) or MUO (n = 39). In the MHO group, the methylation percentage of the <i>LEP</i> gene was significantly higher than in the MUO group, while the <i>LEPR</i> and <i>ADIPOQ</i> genes did not show differences between the study groups. Finally, the methylation of the <i>LEP</i> gene (OR = 1.67; 95% confidence interval (CI): 1.29-2.16; <i>p</i> < 0.001), but not of <i>LEPR</i> (OR = 0.77; 95% CI: 0.45-1.32; <i>p</i> = 0.350) and <i>ADIPOQ</i> (OR = 1.01; 95% CI: 0.97-1.05; <i>p</i> = 0.411), presented a positive association with the MHO phenotype. In conclusion, the <i>LEP</i> gene hypermethylation is positively associated with the MHO phenotype. In addition, the <i>LEPR</i> gene overexpression was significantly associated with the MHO.</p>\",\"PeriodicalId\":520677,\"journal\":{\"name\":\"Journal of investigative medicine : the official publication of the American Federation for Clinical Research\",\"volume\":\" \",\"pages\":\"10815589251378182\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of investigative medicine : the official publication of the American Federation for Clinical Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/10815589251378182\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of investigative medicine : the official publication of the American Federation for Clinical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/10815589251378182","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
据报道,LEP和ADIPOQ基因表观遗传谱中的DNA甲基化与肥胖有关。据我们所知,之前没有关于代谢健康型肥胖(MHO)患者LEP、LEPR和ADIPOQ基因甲基化的报道。因此,本研究的目的是确定LEP、LEPR和ADIPOQ基因的甲基化与MHO表型之间的关系。年龄在20 ~ 55岁、身体质量指数(BMI)≥30 kg/m2的健康男性和女性被纳入病例对照研究。排除标准为妊娠、饮酒、吸烟、糖尿病、高血压、肝病、心血管疾病、肾脏疾病、甲状腺疾病、癌症和/或任何类型的药物治疗。MHO患者被分配到病例组,而代谢不健康肥胖(MUO)患者被分配到对照组。共有78人被纳入,并被分配到MHO组(n=39)和MUO组(n=39)。在MHO组中,LEP基因的甲基化百分比明显高于MUO组,而LEPR和ADIPOQ基因在研究组之间没有差异。最后,LEP基因的甲基化(OR=1.67; 95%CI:1.29-2.16; p
Methylation levels of the LEP, LEPR, and ADIPOQ genes and their association with metabolically healthy obesity.
It has been reported that DNA methylation in the epigenetic profile of the genes LEP and ADIPOQ is associated with obesity. To the best of our knowledge, there are no previous reports assessing the methylation of the LEP, LEPR, and ADIPOQ genes in subjects with metabolically healthy obesity (MHO). Therefore, the aim of this study was to determine the association between methylation of the LEP, LEPR, and ADIPOQ genes with the MHO phenotype. Healthy men and women aged 20-55 years of age with a body mass index ≥30 kg/m2 were enrolled in a case-control study. Exclusion criteria were pregnancy, alcohol intake, smoking, diabetes, hypertension, hepatic disease, cardiovascular disease, renal disease, thyroid disease, cancer, and/or any type of drug therapy. Individuals with MHO were allocated to the case group, while those with metabolically unhealthy obesity (MUO) were assigned to the control group. A total of 78 individuals were enrolled and allocated into the groups with MHO (n = 39) or MUO (n = 39). In the MHO group, the methylation percentage of the LEP gene was significantly higher than in the MUO group, while the LEPR and ADIPOQ genes did not show differences between the study groups. Finally, the methylation of the LEP gene (OR = 1.67; 95% confidence interval (CI): 1.29-2.16; p < 0.001), but not of LEPR (OR = 0.77; 95% CI: 0.45-1.32; p = 0.350) and ADIPOQ (OR = 1.01; 95% CI: 0.97-1.05; p = 0.411), presented a positive association with the MHO phenotype. In conclusion, the LEP gene hypermethylation is positively associated with the MHO phenotype. In addition, the LEPR gene overexpression was significantly associated with the MHO.