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Decreased blood pressure is related to changes in NF-kB promoter methylation levels after bariatric surgery

医学 胰岛素抵抗 袖状胃切除术 甲基化 血压 表观遗传学 炎症 肥胖 内科学 发起人 外科 胃肠病学 内分泌学 生物信息学 胃分流术 基因 减肥 基因表达 遗传学 生物
作者
Manuel Macías‐González,Gracia María Martín‐Núñez,Lourdes Garrido‐Sánchez,Eduardo Garcı́a-Fuentes,Francisco J. Tinahones,Sonsoles Morcillo
出处
期刊:Surgery for Obesity and Related Diseases [Elsevier]
卷期号:14 (9): 1327-1334 被引量:12
标识
DOI:10.1016/j.soard.2018.06.011
摘要

Obesity is characterized by a chronic, low-grade inflammation, and bariatric surgery is proposed as an effective treatment for reducing the obesity-related co-morbidities. Epigenetic modifications could be involved in the metabolic improvement after surgery.The main aim of this study was to evaluate whether DNA methylation pattern from genes related to inflammation and insulin response is associated with the metabolic improvement after bariatric surgery in morbidly obese patients and if these changes depend on the surgical procedure.University hospital, Spain.We studied 60 severely obese patients; 31 underwent Roux-en-Y gastric bypass and 29 underwent laparoscopic sleeve gastrectomy. All patients were examined before and at 6 months after bariatric surgery. DNA methylation profile of genes related to the inflammatory response and insulin sensitivity was measured by pyrosequencing.The promoter methylation levels of the NFKB1 gene were increased significantly after surgery (2.16 ± .9 versus 2.8 ± 1.03). The decrease in blood pressure, both systolic and diastolic, after surgery was significantly associated with the changes in the promoter methylation levels of the NFKB1 gene (β = -.513, P = .003 and β = -.543, P = .004, respectively). A decrease in inflammation status, measured by high sensitivity C-reactive protein values, was associated with changes in SLC19A1 methylation levels.Our study shows for the first time an association between NFKB1 methylation levels and blood pressure after bariatric surgery, highlighting the possible function of this gene in the regulation of arterial pressure. Regarding SLC19A1, this gene could position as a potential target linking inflammation and insulin resistance.
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