Effect of the GHRL gene (rs696217) polymorphism on the metabolic disorders in patients with obesity in the Ukrainian population.

Q3 Medicine Endocrine regulations Pub Date : 2023-09-16 Print Date: 2023-01-01 DOI:10.2478/enr-2023-0021
Andrii Prodan, Ihor Dzubanovsky, Oleksandr Kamyshnyi, Natalia Melnyk, Stepan Grytsenko, Stanislava Voloshyn
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Abstract

Objective. Over the past four decades, the prevalence of obesity has tripled and limited genetic studies with specific SNPs have been conducted, but no investigations using ghrelin and obestatin prepropeptide (GHRL) gene have been reported in the Ukrainians population. The aim of this study was to evaluate changes in the level of metabolic hormones in the blood of obese patients in relation to the GHRL (rs696217) polymorphism. Methods. The study involved 53 obesity cases and 48 non-obesity subjects (controls). The GHRL (rs696217) polymorphism was genotyped using a TaqMan real-time polymerase chain reaction method. Blood hormones were determined with commercially available kits using a Multi-skan FC analyzer. Results. Carriers of the T allele of the GHRL (rs696217) polymorphism were statistically significantly more in patients diagnosed with obesity compared to controls indicating a genetically determined cause of obesity. We also established a significant effect of the presence of the T allele of the GHRL (rs696217) polymorphism on the decrease in the adiponectin level and the increase of resistin level in obese patients. The study of the effect of genotypes (TT, GT, GG) of the GHRL (rs696217) polymorphism on the metabolic hormone levels in the blood of obese patients did not show reliably significant differences. Conclusions. The presence of the T allele of the GHRL (rs696217) polymorphism in Ukrainian population indicates an increased risk of the obesity development regardless on the homozygous or heterozygous genotype.

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GHRL基因(rs696217)多态性对乌克兰人群肥胖患者代谢紊乱的影响。
客观的在过去的四十年里,肥胖的患病率增加了两倍,并且对特定SNPs进行了有限的基因研究,但没有报道在乌克兰人群中使用胃饥饿素和肥胖抑制素前肽(GHRL)基因的研究。本研究的目的是评估肥胖患者血液中代谢激素水平的变化与GHRL(rs696217)多态性的关系。方法。该研究涉及53例肥胖病例和48名非肥胖受试者(对照组)。GHRL(rs696217)多态性采用TaqMan实时聚合酶链式反应方法进行基因分型。使用Multi skan FC分析仪用市售试剂盒测定血液激素。后果GHRL(rs696217)多态性的T等位基因携带者在被诊断为肥胖的患者中比对照组明显多,这表明肥胖的遗传原因。我们还证实了GHRL的T等位基因(rs696217)多态性的存在对肥胖患者脂联素水平下降和抵抗素水平升高的显著影响。GHRL(rs696217)多态性基因型(TT、GT、GG)对肥胖患者血液中代谢激素水平影响的研究没有显示出可靠的显著差异。结论。乌克兰人群中GHRL(rs696217)多态性的T等位基因的存在表明,无论是纯合基因型还是杂合基因型,肥胖发展的风险都会增加。
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来源期刊
Endocrine regulations
Endocrine regulations Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.70
自引率
0.00%
发文量
33
审稿时长
8 weeks
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