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Association of the serotonin transporter-linked polymorphic region genotype with lower bone mineral density

机译:血清素转运蛋白相关的多态性区域基因型与较低的骨矿物质密度的关联

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摘要

The serotonin transporter-linked polymorphic region (5-HTTLPR) of the serotonin transporter gene ( SLC6A4 ) S allele is linked to pathogenesis of depression and slower response to selective serotonin reuptake inhibitors (SSRIs); depression and SSRIs are independently associated with bone loss. We aimed to determine whether 5-HTTLPR was associated with bone loss. This cross-sectional study included psychiatric patients with both 5-HTTLPR analysis and bone mineral density (BMD) assessment (hip and spine Z -scores if age T -scores if ?50 years). BMD association with 5-HTTLPR was evaluated under models with additive allele effects and dominant S allele effects using linear regression models. Patients were stratified by age ( Z -scores at the hip ( P =0.002, dominant S allele effects; P =0.004, additive allele effects) and spine ( P =0.0006, dominant S allele effects; P =0.01, additive allele effects). In sex-stratified analyses, the association of the S allele with lower BMD in the younger patients was also significant in the subset of women ( P ?0.003 for both hip and spine BMD under the additive allele effect model). In the small group of men younger than 50 years, the S allele was marginally associated with higher spine BMD ( P =0.05). BMD T -scores were not associated with 5-HTTLPR genotypes in patients 50 years or older. The 5-HTTLPR variants may modify serotonin effects on bone with sex-specific effects.
机译:血清素转运蛋白基因(SLC6A4)S等位基因的5-羟色胺转运蛋白连锁多态性区域(5-HTTLPR)与抑郁症的发病机制有关,对选择性5-羟色胺再摄取抑制剂(SSRIs)的反应较慢;抑郁症和SSRI与骨质流失独立相关。我们旨在确定5-HTTLPR是否与骨质流失有关。这项横断面研究包括接受5-HTTLPR分析和骨矿物质密度(BMD)评估的精神病患者(如果年龄≥50岁,则髋关节和脊柱Z分数为T分数)。使用线性回归模型在具有加性等位基因效应和显性S等位基因效应的模型下评估BMD与5-HTTLPR的关联。按年龄(髋部Z评分(P = 0.002,主要S等位基因效应; P = 0.004,附加等位基因效应)和脊柱(P = 0.0006,主要S等位基因效应; P = 0.01,附加等位基因效应)对患者进行分层。 。在按性别分层的分析中,年轻亚型患者中S等位基因与较低BMD的关联在女性亚组中也很显着(在加性等位基因效应模型下,髋部和脊柱BMD的P≥0.003)。在50岁以下的男性中,S等位基因与较高的脊柱BMD相关(P = 0.05); BMD T得分与50岁或以上的患者的5-HTTLPR基因型无关; 5-HTTLPR变异可能会修饰血清素对骨骼有特殊的影响。

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