自闭症谱系障碍的基因变异与血清中瘦素和胃泌素的水平。

IF 0.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Psychiatry and Clinical Psychopharmacology Pub Date : 2024-09-01 DOI:10.5152/pcp.2024.24827
Özlem Nehir Yazici, Nilfer Şahin, Çilem Özdemir, Ercan Saruhan, Hatice Topal, Tarkan Yazıcı, Özge Dombaycı, Gülsüm Demirkan Başkaya, Tuba Edgünlü
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引用次数: 0

摘要

研究背景本研究旨在探讨自闭症谱系障碍(ASD)儿童的瘦素和胃泌素基因多态性及血清水平:研究包括一个病例组(40 名 2-7 岁被诊断为 ASD 的儿童)和一个对照组(40 名健康儿童)。自闭症症状的严重程度通过儿童自闭症评定量表和自闭症行为核对表进行评估。使用聚合酶链式反应(PCR)限制性片段长度多态性(RFLP)方法对瘦素和胃泌素基因变异进行了基因分型。使用酶联免疫吸附测定试剂盒测定血清胃泌素和瘦素水平:本研究对基因多态性和等位基因频率进行了检测,未发现显著差异(P > .05)。研究结果表明,各组间瘦素血清水平无明显差异(P = .584)。然而,ASD 组的胃泌素血清水平明显较低(P = .027)。通过接收者操作曲线分析,确定了作为 ASD 诊断指标的血清胃泌素水平的临界值为 885.7 pg/mL,灵敏度为 42.50%,特异度为 85% (P = .021)。在瘦素和胃泌素血清水平与ASD严重程度之间没有发现明显的关系(均为P > .05):我们的研究首次评估了 ASD 中瘦素和胃泌素基因的多态性。我们的研究结果表明,瘦素和胃泌素基因多态性与 ASD 之间没有关联。然而,我们的研究表明,胃泌素血清水平可能是导致 ASD 病因的潜在因素。要了解瘦素和胃泌素在 ASD 中的作用,还需要进行更多的研究。
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Genetic Variations and Serum Levels of Leptin and Ghrelin in Autism Spectrum Disorder.

Background: This study aims to examine leptin and ghrelin gene polymorphisms and serum levels in children with autism spectrum disorder (ASD).

Methods: The study comprised a case group of 40 children aged 2-7 diagnosed with ASD and a control group of 40 healthy children. The severity of ASD symptoms was assessed using the Childhood Autism Rating Scale and the Autism Behavior Checklist. Leptin and ghrelin gene variants were genotyped using polymerase chain reaction (PCR) restriction fragment length polymorphism (RFLP) methods. Serum ghrelin and leptin levels were measured using enzyme-linked immunosorbent assay kits.

Results: In this study, gene polymorphisms and allele frequencies were examined, and no significant difference was found (P > .05 for all). Our findings indicated no significant difference in leptin serum levels between the groups (P = .584). However, ghrelin serum levels were significantly lower in the ASD group (P = .027). Receiver operating curve analysis to determine the cutoff value of serum ghrelin level as a diagnostic indicator for ASD resulted in a cutoff value of 885.7 pg/mL with 42.50% sensitivity and 85% specificity (P = .021). No significant relationship was found between leptin and ghrelin serum levels and the severity of ASD (P > .05 for all).

Conclusion: Our study is the first to evaluate leptin and ghrelin gene polymorphisms in ASD. Our findings indicate no association between leptin and ghrelin gene polymorphisms and ASD. However, our study suggests that ghrelin serum levels may potentially contribute to the etiology of ASD. More research is needed to understand the role of leptin and ghrelin in ASD.

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来源期刊
Psychiatry and Clinical Psychopharmacology
Psychiatry and Clinical Psychopharmacology Medicine-Psychiatry and Mental Health
CiteScore
1.00
自引率
14.30%
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期刊介绍: Psychiatry and Clinical Psychopharmacology aims to reach a national and international audience and will accept submissions from authors worldwide. It gives high priority to original studies of interest to clinicians and scientists in applied and basic neurosciences and related disciplines. Psychiatry and Clinical Psychopharmacology publishes high quality research targeted to specialists, residents and scientists in psychiatry, psychology, neurology, pharmacology, molecular biology, genetics, physiology, neurochemistry, and related sciences.
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