Please use this identifier to cite or link to this item: http://hdl.handle.net/10668/11075
Title: Changes in SCD gene DNA methylation after bariatric surgery in morbidly obese patients are associated with free fatty acids.
Authors: Morcillo, Sonsoles
Martín-Núñez, Gracia Mª
García-Serrano, Sara
Gutierrez-Repiso, Carolina
Rodriguez-Pacheco, Francisca
Valdes, Sergio
Gonzalo, Montserrat
Rojo-Martinez, Gemma
Moreno-Ruiz, Francisco J
Rodriguez-Cañete, Alberto
Tinahones, Francisco
García-Fuentes, Eduardo
metadata.dc.subject.mesh: Adult
Bariatric Surgery
DNA Methylation
Epigenesis, Genetic
Fatty Acids, Nonesterified
Female
Gene Expression Regulation
Humans
Insulin Resistance
Male
Middle Aged
Obesity, Morbid
Promoter Regions, Genetic
RNA, Messenger
Stearoyl-CoA Desaturase
Issue Date: 10-Apr-2017
Abstract: Stearoyl CoA Desaturase-1 (SCD) is considered as playing an important role in the explanation of obesity. The aim of this study was to evaluate whether the DNA methylation SCD gene promoter is associated with the metabolic improvement in morbidly obese patients after bariatric surgery. The study included 120 subjects with morbid obesity who underwent a laparoscopic Roux-en Y gastric by-pass (RYGB) and a control group of 30 obese subjects with a similar body mass index (BMI) to that found in morbidly obese subjects six months after RYGB. Fasting blood samples were obtained before and at six months after RYGB. DNA methylation was measured by pyrosequencing technology. DNA methylation levels of the SCD gene promoter were lower in morbidly obese subjects before bariatric surgery but increased after RYGB to levels similar to those found in the control group. Changes of DNA methylation SCD gene were associated with the changes of free fatty acids levels (r = -0.442, p = 0.006) and HOMA-IR (r = -0.249, p = 0.035) after surgery. RYGB produces an increase in the low SCD methylation promoter levels found in morbidly obese subjects. This change of SCD methylation levels is associated with changes in FFA and HOMA-IR.
URI: http://hdl.handle.net/10668/11075
metadata.dc.identifier.doi: 10.1038/srep46292
Appears in Collections:Producción 2020

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