种族解释了全血硫胺素二磷酸浓度的大量差异。

Race explains substantial variance in whole blood thiamine diphosphate concentrations.

机构信息

Department of Psychiatry & Behavioral Sciences, Stanford University, School of Medicine, Stanford, CA 94305, USA; Neuroscience Program, SRI International, Menlo Park, CA, 94025, USA.

出版信息

Nutr Res. 2024 Jun;126:138-150. doi: 10.1016/j.nutres.2024.03.011. Epub 2024 Mar 30.

Abstract

Deficiency for thiamine (vitamin B), traditionally assessed via the activity of the thiamine-dependent enzyme erythrocyte transketolase, has been reported in individuals with alcohol use disorder (AUD) and in people with HIV; concentrations of the metabolically active diphosphate form, however, have yet to be reported in HIV cohorts and results in AUD are equivocal. In this cross-sectional study, samples from 170 AUD, 130 HIV, and 100 healthy control individuals were analyzed to test the hypothesis that AUD and HIV groups relative to healthy controls would show low whole blood thiamine diphosphate (TDP) concentrations related to peripheral neuropathy. TDP concentrations were not different in the 3 study groups (P = .6141) but were lower in Black (n = 172) relative to White (n = 155) individuals (P < .0001) regardless of group. In a multiple regression, race relative to diagnoses explained more than 10 times the variance in whole blood TDP concentrations (F = 3.5, P = .0086; r = 15.1]. Performance on a measure of peripheral neuropathy (2-point discrimination) was worse in the HIV and AUD cohorts relative to the healthy control group (P < .0001) but was not associated with TDP concentrations. These findings suggest that Black individuals carry a heightened vulnerability for low whole blood TDP concentrations, but the clinical significance and mechanisms underlying these results remain to be determined.

摘要

硫胺素(维生素 B)缺乏症,传统上通过测定依赖硫胺素的红细胞转酮醇酶的活性来评估,在患有酒精使用障碍(AUD)和 HIV 的个体中已有报道;然而,HIV 患者群体中尚未报道代谢活跃的二磷酸形式的浓度,并且 AUD 的结果存在争议。在这项横断面研究中,分析了 170 名 AUD、130 名 HIV 和 100 名健康对照个体的样本,以检验以下假设:与健康对照组相比,AUD 和 HIV 组会表现出与周围神经病变相关的低全血硫胺素二磷酸(TDP)浓度。3 个研究组的 TDP 浓度没有差异(P =.6141),但无论组别如何,黑人(n = 172)的 TDP 浓度均低于白人(n = 155)个体(P <.0001)。在多元回归中,相对于诊断,种族解释了全血 TDP 浓度方差的 10 倍以上(F = 3.5,P =.0086;r = 15.1])。与健康对照组相比,HIV 和 AUD 队列的周围神经病变(两点辨别)测量结果更差(P <.0001),但与 TDP 浓度无关。这些发现表明,黑人个体携带低全血 TDP 浓度的风险增加,但这些结果的临床意义和潜在机制仍有待确定。

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