Serum miRNA levels are related to glucose homeostasis and islet autoantibodies in children with high risk for type 1 diabetes

被引:45
作者
Akerman, Linda [1 ]
Casas, Rosaura [1 ]
Ludvigsson, Johnny [1 ,2 ]
Tavira, Beatriz [1 ]
Skoglund, Camilla [3 ]
机构
[1] Linkoping Univ, Fac Med & Hlth Sci, Dept Clin & Expt Med, Div Pediat, Linkoping, Sweden
[2] Univ Hosp, Crown Princess Victoria Childrens Hosp, Linkoping, Region Ostergot, Sweden
[3] Linkoping Univ, Fac Med & Hlth Sci, Dept Med & Hlth Sci, Div Drug Res, Linkoping, Sweden
来源
PLOS ONE | 2018年 / 13卷 / 01期
基金
瑞典研究理事会; 英国医学研究理事会;
关键词
BLOOD MONONUCLEAR-CELLS; MICRORNAS; EXPRESSION; DYSFUNCTION; BIOMARKERS; FAMILY; TARGET;
D O I
10.1371/journal.pone.0191067
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Micro RNAs (miRNAs) are promising disease biomarkers due to their high stability. Their expression in serum is altered in type 1 diabetes, but whether deviations exist in individuals with high risk for type 1 diabetes remains unexplored. We therefore assessed serum miRNAs in high-risk individuals (n = 21) positive for multiple islet autoantibodies, age-matched healthy children (n = 17) and recent-onset type 1 diabetes patients (n = 8), using Serum/Plasma Focus microRNA PCR Panels from Exiqon. The miRNA levels in the high-risk group were similar to healthy controls, and no specific miRNA profile was identified for the high-risk group. However, serum miRNAs appeared to reflect glycemic status and ongoing islet auto-immunity in high-risk individuals, since several miRNAs were associated to glucose homeostasis and autoantibody titers. High-risk individuals progressing to clinical disease after the sampling could not be clearly distinguished from non-progressors, while miRNA expression in the type 1 diabetes group deviated significantly from high-risk individuals and healthy controls, perhaps explained by major metabolic disturbances around the time of diagnosis.
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页数:15
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