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本文引用的文献

1
Possible association between G-protein β3 subunit C825T polymorphism and antipsychotic-induced restless legs syndrome in schizophrenia.G蛋白β3亚基C825T多态性与精神分裂症患者抗精神病药物所致不安腿综合征之间的可能关联。
Acta Neuropsychiatr. 2007 Dec;19(6):351-6. doi: 10.1111/j.1601-5215.2007.00240.x.
2
Association between restless legs syndrome and CLOCK and NPAS2 gene polymorphisms in schizophrenia.精神分裂症中不宁腿综合征与CLOCK和NPAS2基因多态性之间的关联。
Chronobiol Int. 2014 Aug;31(7):838-44. doi: 10.3109/07420528.2014.914034. Epub 2014 May 14.
3
Association of candidate genetic variants with restless legs syndrome in end stage renal disease: a multicenter case-control study in Taiwan.候选基因变异与终末期肾病患者不宁腿综合征的相关性:台湾多中心病例对照研究。
Eur J Neurol. 2014 Mar;21(3):492-8. doi: 10.1111/ene.12337. Epub 2014 Jan 16.
4
The BTBD9 gene may be associated with antipsychotic-induced restless legs syndrome in schizophrenia.BTBD9基因可能与精神分裂症患者中抗精神病药物诱发的不宁腿综合征有关。
Hum Psychopharmacol. 2013 Mar;28(2):117-23. doi: 10.1002/hup.2287. Epub 2013 Jan 30.
5
Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis.不宁腿综合征相关 MEIS1 风险变异影响铁稳态。
Ann Neurol. 2011 Jul;70(1):170-5. doi: 10.1002/ana.22435. Epub 2011 Jun 27.
6
MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease.MEIS1 和 BTBD9:与终末期肾病不宁腿综合征的遗传关联。
J Med Genet. 2011 Jul;48(7):462-6. doi: 10.1136/jmg.2010.087858. Epub 2011 May 14.
7
Association study between antipsychotic-induced restless legs syndrome and polymorphisms of monoamine oxidase genes in schizophrenia.精神分裂症患者中抗精神病药物所致不宁腿综合征与单胺氧化酶基因多态性的关联研究
Hum Psychopharmacol. 2010 Jul;25(5):397-403. doi: 10.1002/hup.1130.
8
Association between Antipsychotics-Induced Restless Legs Syndrome and Tyrosine Hydroxylase Gene Polymorphism.抗精神病药所致不宁腿综合征与酪氨酸羟化酶基因多态性的关联。
Psychiatry Investig. 2009 Sep;6(3):211-5. doi: 10.4306/pi.2009.6.3.211. Epub 2009 Jul 15.
9
[Secondary restless legs syndrome].[继发性不宁腿综合征]
Brain Nerve. 2009 May;61(5):539-47.
10
Replication of restless legs syndrome loci in three European populations.不安腿综合征基因座在三个欧洲人群中的复制情况。
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MEIS1,一个有前途的候选基因,与韩国精神分裂症患者抗精神病药引起的不安腿综合征的核心症状无关。

MEIS1, a Promising Candidate Gene, Is Not Associated with the Core Symptoms of Antipsychotic-Induced Restless Legs Syndrome in Korean Schizophrenia Patients.

机构信息

Department of Psychiatry, Gil Medical Center, Gachon University School of Medicine, Incheon, Republic of Korea.

Department of Psychiatry, Korea University College of Medicine, Seoul, Republic of Korea.

出版信息

Psychiatry Investig. 2015 Apr;12(2):263-7. doi: 10.4306/pi.2015.12.2.263. Epub 2015 Mar 18.

DOI:10.4306/pi.2015.12.2.263
PMID:25866529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4390599/
Abstract

OBJECTIVE

Restless legs syndrome (RLS) is a distressing sleep disorder to which individuals appear to be genetically predisposed. In the present study, we assumed that antipsychotic-induced RLS symptoms were attributable to differences in individual genetic susceptibility, and investigated whether MEIS1, a promising candidate gene, was associated with antipsychotic-induced RLS symptoms in schizophrenia patients.

METHODS

All subjects were diagnosed with schizophrenia by board-certified psychiatrists using the Korean version of the Structured Clinical Interview for DSM-IV. We assessed antipsychotic-induced RLS symptoms in 190 Korean schizophrenic patients using the diagnostic criteria of the International Restless Legs Syndrome Study Group. Genotyping was performed for the rs2300478 and rs6710341 polymorphisms of the MEIS1 gene.

RESULTS

We divided subjects into RLS symptom (n=96) and non-symptom (n=94) groups. There was no significant between-group difference in the genotype or allele frequencies of the two polymorphisms investigated, nor in the frequency of the rs2300478-rs6710341 haplotype.

CONCLUSION

Our data do not suggest that the rs2300478 and rs6710341 polymorphisms of the MEIS1 gene are associated with the core symptoms of antipsychotic-induced RLS in schizophrenia; different genetic mechanisms may underlie antipsychotic-induced vs. primary RLS.

摘要

目的

不宁腿综合征(RLS)是一种令人痛苦的睡眠障碍,个体似乎对此存在遗传易感性。本研究假设抗精神病药引起的 RLS 症状归因于个体遗传易感性的差异,并探讨 MEIS1 这一有前途的候选基因是否与精神分裂症患者抗精神病药引起的 RLS 症状相关。

方法

所有受试者均由经过董事会认证的精神科医生通过使用 DSM-IV 韩国版结构化临床访谈进行精神分裂症诊断。我们使用国际不宁腿综合征研究组的诊断标准,对 190 名韩国精神分裂症患者的抗精神病药引起的 RLS 症状进行评估。对 MEIS1 基因的 rs2300478 和 rs6710341 多态性进行基因分型。

结果

我们将受试者分为 RLS 症状(n=96)和非症状(n=94)组。两个研究的多态性的基因型或等位基因频率以及 rs2300478-rs6710341 单倍型频率在两组之间均无显著差异。

结论

我们的数据表明,MEIS1 基因的 rs2300478 和 rs6710341 多态性与精神分裂症中抗精神病药引起的 RLS 的核心症状无关;抗精神病药引起的 RLS 与原发性 RLS 的遗传机制可能不同。