Evaluation of IGFBP-7 DNA methylation changes and serum protein variation in Swedish subjects with and without type 2 diabetes

被引:36
作者
Gu, Harvest F. [1 ]
Gu, Tianwei [1 ]
Hilding, Agneta [1 ]
Zhu, Yiming [2 ]
Karvestedt, Lars [1 ]
Ostenson, Claes-Goran [1 ]
Lai, Maode [2 ]
Kutsukake, Masahiko [3 ]
Frystyk, Jan [4 ,5 ]
Tamura, Kazuhiro [3 ]
Brismar, Kerstin [1 ]
机构
[1] Karolinska Inst, Karolinska Univ Hosp, Rolf Luft Res Ctr Diabet & Endocrinol, Dept Mol Med & Surg, SE-17176 Stockholm, Sweden
[2] Zhejiang Univ, Sch Med, Dept Mol Pathol, Hangzhou 310003, Zhejiang, Peoples R China
[3] Tokyo Univ Pharm & Life Sci, Dept Endocrine Pharmacol, Tokyo, Japan
[4] Aarhus Univ, Fac Hlth, Dept Clin Med, Med Res Lab, Aarhus, Denmark
[5] Aarhus Univ Hosp, Dept Endocrinol & Internal Med, DK-8000 Aarhus, Denmark
基金
瑞典研究理事会;
关键词
IGF-1; IGFBP-1; IGFBP-7; Insulin; Type; 2; diabetes; FACTOR-BINDING PROTEIN-1; GROWTH-FACTOR-I; IGF-I; INSULIN; RISK; EPIGENETICS; IMPROVEMENT; ENDOCRINE; MELLITUS; HORMONE;
D O I
10.1186/1868-7083-5-20
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Insulin-like growth factor-binding protein 7 (IGFBP-7) is able to interact with insulin-like growth factor 1 (IGF-1) as well as insulin. Previous studies have suggested that serum IGFBP-7 levels may be associated with insulin resistance in type 2 diabetes (T2D). This study aimed to evaluate IGFBP-7 serum protein and IGFBP7 DNA methylation levels in the subjects with and without T2D. Results: A total of 340 Swedish subjects including 100 newly diagnosed T2D patients (50 women/50 men), 100 age-matched nondiabetic control subjects (50/50) and 140 treated T2D patients (54/86) were studied. Serum IGFBP-7 levels were measured with a novel ELISA. IGF1, IGFBP-1, and insulin were determined by in-house radioimmunoassays. DNA methylation levels in the IGFBP7 gene were analyzed with a bisulfite-pyrosequencing technique. Serum IGFBP-7 protein levels were similar among nondiabetic subjects, newly diagnosed, and treated T2D patients and were not correlated with IGFBP7 DNA methylation. However, IGFBP7 DNA methylation was increased in men with newly diagnosed T2D compared with nondiabetic controls (17.6% vs. 12.5%, P < 0.01). Serum IGFBP-7 levels correlated (r = 0.331, P = 0.019) with serum IGFBP-1 levels, a marker of insulin production, in men but not women with newly diagnosed T2D. Conclusions: This study demonstrates for the first time that IGFBP7 DNA methylation levels are increased in Swedish men with newly diagnosed T2D. The correlation between IGFBP-7 and IGFBP-1 suggests that low IGFBP-7 may be associated with insulin resistance in T2D.
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页数:7
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