Role of miRNA Gene Variants (miR-22 and miR-155) as the Factors Affecting Susceptibility to Panic Disorder.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-11-30 Epub Date: 2024-08-28 DOI:10.9758/cpn.24.1201
Zeynep Yegin, Gokhan Sarisoy, Ahmet Uzun, Haydar Koc
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Abstract

Objective: Variants within genes encoding microRNAs (miRNAs) may alter the expression of both miRNAs and their target genes, thus contributing to the etiology of psychiatric disorders. The involvement of miRNAs in neuronal differentiation and synaptic plasticity supported this hypothesis. We aimed to investigate the links between miR-155 rs767649/miR-22 rs8076112 and the risk of panic disorder (PD) in a sample of Turkish population.

Methods: In this experimental study, 134 PD patients and 140 healthy controls were recruited. Genotyping was carried out using Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) method. To evaluate PD phenotypes, Panic Disorder Severity Scale (PDSS) was also administered to patients to clarify possible associations between the scale and risk variants analyzed.

Results: The genotype analysis of miR-155 rs767649 did not show an association with PD risk and it was not related to the disease severity. For miR-22 rs8076112 variant, a statistically significant association was determined; CC genotypes were lower in patients compared to controls. Logistic regression analysis proved the highly protective effect (80.4%) of CC genotype against PD (p = 0.041; OR = 0.196, 95% CI = 0.041-0.934). Though its significance in disease liability, miR-22 rs8076112 was not associated with the disease severity.

Conclusion: Our findings firstly report the combined analysis of miR-155 rs767649 and miR-22 rs8076112 in PD in terms of both disease susceptibility and severity. These findings await replication in independent cohorts with enrichment of other miRNA gene variants. Thus, certain miRNAs and their target genes involved in the etiology and phenotypes of PD could be enlightened.

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miRNA 基因变异(miR-22 和 miR-155)是影响恐慌症易感性的因素。
目的:编码微RNA(miRNA)基因的变异可能会改变miRNA及其靶基因的表达,从而导致精神疾病的病因。miRNA 参与神经元分化和突触可塑性的研究支持了这一假设。我们的目的是在土耳其人群中调查 miR-155 rs767649/miR-22 rs8076112 与惊恐障碍(PD)风险之间的联系:在这项实验研究中,共招募了 134 名 PD 患者和 140 名健康对照者。采用聚合酶链式反应-限制性片段长度多态性(PCR-RFLP)方法进行基因分型。为了评估帕金森氏症的表型,还对患者进行了恐慌症严重程度量表(PDSS)测试,以明确该量表与所分析的风险变异之间可能存在的关联:结果:miR-155 rs767649的基因型分析未显示与帕金森氏症风险有关,也与疾病严重程度无关。miR-22 rs8076112变异与帕金森病有统计学意义;与对照组相比,患者的CC基因型较低。逻辑回归分析证明,CC 基因型对帕金森病具有高度保护作用(80.4%)(p = 0.041;OR = 0.196,95% CI = 0.041-0.934)。尽管miR-22 rs8076112在疾病责任中具有重要意义,但它与疾病的严重程度无关:我们的研究结果首次综合分析了 miR-155 rs767649 和 miR-22 rs8076112 在帕金森病中对疾病易感性和严重程度的影响。这些研究结果有待在富含其他 miRNA 基因变异的独立队列中复制。因此,某些与帕金森病的病因学和表型有关的 miRNA 及其靶基因可以得到启示。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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