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PAX4 R192H 是与特定种族 2 型糖尿病风险因素相关的基因,该突变与中国 2 型糖尿病患者的注意力特异性认知障碍有关。

Ethnic-Specific Type 2 Diabetes Risk Factor PAX4 R192H Is Associated with Attention-Specific Cognitive Impairment in Chinese with Type 2 Diabetes.

机构信息

Clinical Research Unit, Khoo Teck Puat Hospital (KTPH), Singapore.

Department of Psychological Medicine, Gerontology Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

出版信息

J Alzheimers Dis. 2022;88(1):241-249. doi: 10.3233/JAD-220036.

Abstract

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.

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β细胞发育和功能的转录因子,最近与阿尔茨海默病和 T2DM 相交的途径有关。

目的

在本报告中,我们评估了东亚 2 型糖尿病的危险因素、PAX4 R192H 变体与中国 2 型糖尿病患者认知功能的相关性。

方法

SMART2D 研究中,使用 Illumina OmniExpress-24 阵列对 590 名年龄在 45-86 岁的中国患者进行 PAX4 R192H 变异的基因分型。重复神经心理状态评估测试(RBANS),该测试已在新加坡人群中得到验证,用于评估五个认知领域:即刻记忆、视空间/结构、语言、注意力和延迟记忆。使用多元线性回归来评估 R192H 风险等位基因与认知领域的关联。

结果

调整年龄、性别、糖尿病发病年龄、HbA1c、体重指数、肾功能、血脂谱、收缩压、二甲双胍使用情况、吸烟史、教育程度、老年抑郁量表评分和 APOEɛ4 等位基因后,携带两个 PAX4 R192H 风险等位基因的患者注意力指数评分明显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 中的种族特异性 R192H 变异与中国 2 型糖尿病患者注意力特异性认知障碍有关。在进一步的验证研究中,确定 PAX4 R192H 基因型可能有助于对早发性 2 型糖尿病和认知障碍进行早期风险评估,从而改善糖尿病的护理。

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