Department of Psychiatry, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, No. 123, Dapi Rd., Niaosong District, Kaohsiung City, 833, Taiwan.
Graduate Institute of Biomedical Sciences, China Medical University, No. 91, Hsueh-Shih Rd., North Dist., Taichung City, 404, Taiwan.
Sci Rep. 2020 Aug 6;10(1):13236. doi: 10.1038/s41598-020-70262-0.
Schizophrenia patients are susceptible to lower bone mineral density (BMD). However, studies exploring the genetic effects are lacking. Genes that affect the activity of antipsychotics may be associated with BMD, particularly in patients receiving long-term antipsychotic treatment. We aimed to explore the relationship between the dopamine receptor D (DRD2) gene Taq1A (rs1800497) polymorphism and BMD in chronic schizophrenia patients. We recruited schizophrenia patients (n = 47) and healthy controls (n = 39) from a medical center in Taiwan and collected data that may affect BMD. Patients' BMD was measured by dual-energy X-ray absorptiometer (DEXA). DRD2 rs1800497 was genotyped through polymerase chain reaction-Restriction Fragment Length Polymorphism (PCR-RFLP). Among all participants, subjects with DRD2 rs1800497(T;T) allele had lower DEXA T score and DEXA Z score compared to those with rs1800497(C;T) and rs1800497(C;C) alleles (p = 0.008, 0.003, respectively). In schizophrenia patients, subjects with rs1800497(T;T) allele also had lower DEXA Z score compared to the other two alleles (p = 0.045). Our findings suggest that individuals with the DRD2 rs1800497(T;T) had lower BMD than those with the rs1800497(C;T) and rs1800497(C;C) genotypes. Therefore, genes should be considered as one of the risk factors of lower BMD.
精神分裂症患者易出现较低的骨密度(BMD)。然而,目前缺乏探索遗传因素影响的研究。影响抗精神病药活性的基因可能与 BMD 相关,尤其是在接受长期抗精神病治疗的患者中。我们旨在探讨慢性精神分裂症患者多巴胺受体 D(DRD2)基因 Taq1A(rs1800497)多态性与 BMD 的关系。我们从台湾一家医疗中心招募了精神分裂症患者(n=47)和健康对照者(n=39),并收集了可能影响 BMD 的数据。通过双能 X 射线吸收仪(DEXA)测量患者的 BMD。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测 DRD2 rs1800497 基因分型。在所有参与者中,与携带 rs1800497(C;T)和 rs1800497(C;C)等位基因的个体相比,携带 DRD2 rs1800497(T;T)等位基因的个体 DEXA T 评分和 DEXA Z 评分较低(p=0.008,0.003)。在精神分裂症患者中,与其他两种等位基因相比,携带 rs1800497(T;T)等位基因的个体的 DEXA Z 评分也较低(p=0.045)。我们的研究结果表明,与携带 rs1800497(C;T)和 rs1800497(C;C)基因型的个体相比,携带 DRD2 rs1800497(T;T)等位基因的个体的 BMD 较低。因此,基因应被视为较低 BMD 的风险因素之一。