民族特异性2型糖尿病危险因子PAX4 R192H与中国2型糖尿病患者注意特异性认知障碍相关

S. Ang, Serena Low, T. Ng, Clara S. H. Tan, K. Ang, Ziliang Lim, W. Tang, T. Subramaniam, C. Sum, S. Lim
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摘要

背景:2型糖尿病(T2DM)已被证明会增加认知能力下降和痴呆的风险。配对盒基因4 (PAX4)是一种β细胞发育和功能的转录因子,最近被认为与阿尔茨海默病和T2DM的交叉通路有关。目的:在本报告中,我们评估了种族特异性PAX4 R192H变异与中国T2DM患者认知功能的关系。PAX4 R192H变异是东亚人早期糖尿病发病的危险因素。方法采用Illumina OmniExpress-24 Array对来自SMART2D研究的s590例45-86岁的中国患者进行PAX4 R192H变异基因分型。在新加坡人群中得到验证的神经心理状态评估可重复电池(rban)被用于评估五个认知领域:即时记忆、视觉空间/结构、语言、注意力和延迟记忆。采用多元线性回归评估R192H风险等位基因与认知领域的关系。结果在调整年龄、性别、糖尿病发病年龄、HbA1c、体质量指数、肾功能、血脂、收缩压、二甲双胍使用情况、吸烟史、文化程度、老年抑郁量表评分、APOE / 4等位基因存在等因素后,携带2个PAX4 R192H危险等位基因的患者的注意力指数得分显著低于携带野生型等位基因的患者(β= -8.46, 95% CI [-13.71, -3.21], p = 0.002)。结论PAX4基因R192H的种族特异性变异与中国T2DM患者的注意特异性认知障碍有关。在进一步的验证研究中,确定PAX4 R192H基因型可能有助于早发性T2DM和认知障碍的早期风险评估,从而改善糖尿病的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ethnic-Specific Type 2 Diabetes Risk Factor PAX4 R192H Is Associated with Attention-Specific Cognitive Impairment in Chinese with Type 2 Diabetes.
BACKGROUND Type 2 diabetes mellitus (T2DM) has been shown to increase the risks of cognitive decline and dementia. Paired box gene 4 (PAX4), a transcription factor for beta cell development and function, has recently been implicated in pathways intersecting Alzheimer's disease and T2DM. OBJECTIVE In this report, we evaluated the association of the ethnic-specific PAX4 R192H variant, a T2DM risk factor for East Asians which contributes to earlier diabetes onset, and cognitive function of Chinese T2DM patients. METHODS 590 Chinese patients aged 45-86 from the SMART2D study were genotyped for PAX4 R192H variation using Illumina OmniExpress-24 Array. The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) which had been validated in the Singapore population was administered to assess five cognitive domains: immediate memory, visuospatial/constructional, language, attention, and delayed memory. Multiple linear regression was used to assess the association of the R192H risk allele and cognitive domains. RESULTS Patients with two PAX4 R192H risk alleles showed significantly lower attention index score (β= -8.46, 95% CI [-13.71, -3.21], p = 0.002) than patients with wild-type alleles after adjusting for age, gender, diabetes onset age, HbA1c, body-mass index, renal function, lipid profiles, systolic blood pressure, metformin usage, smoking history, education level, Geriatric Depression Scale score, and presence of APOEɛ4 allele. CONCLUSION Ethnic-specific R192H variation in PAX4 is associated with attention-specific cognitive impairment in Chinese with T2DM. Pending further validation studies, determining PAX4 R192H genotype may be helpful for early risk assessment of early-onset T2DM and cognitive impairment to improve diabetes care.
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