循环 miR-323-3p 作为中老年人多病负担和认知能力下降的潜在新型血浆生物标记物:日本国立长寿科学研究所老龄化纵向研究的结果

Wei-Min Chu , Mio Goto , Keiko Kabetani , Yukiko Nishita , Shu Zhang , Hiroshi Shimokata , Meng-Chih Lee , Akiko Satoh , Rei Otsuka
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引用次数: 0

摘要

背景血液中的几种循环微RNA(miRNA)是慢性疾病的指标,但它们与多病负担的关系尚不清楚。本研究旨在评估中老年人血浆中循环 miR-323-3p 和 miR-135-3p 的水平与年龄、认知能力和合并症数量的关系。从血浆中分离出 miRNA,用定量反转录聚合酶链反应法测定 miR-323-3p 和 miR-135-3p 的水平,并以 miR-16 作为内源性参考基因进行归一化处理。认知能力采用韦氏成人智能量表-修订简表(WAIS-R-SF)的信息和相似性分测验和数字符号替换测验进行评估。研究人员进行了相关性检验和多变量一般线性回归分析,以探讨循环 miRNA 水平、多病负担和认知能力之间的关系。皮尔逊相关分析表明,miR-323-3p水平与年龄和合并症数量呈正相关,但与WAIS-R-SF分测验成绩呈负相关。在男性中,miR-323-3p 水平与 WAIS-R-SF 所有三个分测验的成绩呈负相关。一般线性回归分析表明,与患有一种疾病的人相比,患有四种疾病的人的 miR-323-3p 水平会升高。
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Circulating miR-323–3p as a novel potential plasma biomarker for multimorbidity burden and cognitive decline in middle-aged and older adults: Results from the national institute for longevity sciences–longitudinal study of aging in Japan

Background

Several circulating microRNAs (miRNAs) in the blood are indicators of chronic diseases, but their association with multimorbidity burden is unknown. The aim of this study was to assess the association of plasma levels of circulating miR-323–3p and miR-135–3p with age, cognitive performance, and number of comorbidities in middle-aged and older individuals.

Methods

Data from 295 community dwellers (≥40 years) who participated in the second wave (2000‒2002) of the National Institute for Longevity Sciences-Longitudinal Study of Aging in Japan were analyzed. miRNAs were isolated from the plasma, and miR-323–3p and miR-135–3p levels were measured using quantitative reverse-transcription polymerase chain reaction and normalized, with miR-16 as an endogenous reference gene. Cognitive performance was assessed using the Information and Similarities subtests and the Digit Symbol Substitution Test of the Wechsler Adult Intelligence Scale-Revised Short Form (WAIS-R-SF). Correlation tests and multivariate general linear regression analyses were performed to examine the relationship among circulating miRNA levels, burden of multimorbidity, and cognitive performance.

Results

The mean age of the participants was 59.15 ± 10.26 years. Pearson's correlation analysis revealed that the miR-323–3p level positively correlated with age and number of comorbidities but negatively correlated with WAIS-R-SF subtest performance. In men, miR-323–3p level negatively correlated with the performance of all three WAIS-R-SF subtests. The general linear regression analysis showed that the miR-323–3p level increased in participants with four comorbidities compared with those with one comorbidity.

Conclusion

Circulating miR-323–3p level is associated with the burden of multimorbidity and decreased cognitive performance in middle-aged and older adults.
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