Comparison of Immunoassays for the Selective Measurement of Human High-Molecular Weight Adiponectin

被引:11
|
作者
Liu, Dan [1 ,2 ]
Schuster, Tibor [3 ]
Baumann, Marcus [1 ]
Roos, Marcel [1 ]
Sollinger, Daniel [1 ]
Lutz, Jens [1 ]
Heemann, Uwe [1 ]
von Eynatten, Maximilian [1 ]
机构
[1] Tech Univ Munich, Dept Nephrol, D-81675 Munich, Germany
[2] Sun Yat Sen Univ, Dept Endocrinol, Hosp 2, Guangzhou 510275, Guangdong, Peoples R China
[3] Tech Univ Munich, Inst Med Stat & Epidemiol, Munich, Germany
关键词
LINKED-IMMUNOSORBENT-ASSAY; CORONARY-ARTERY-DISEASE; INSULIN-RESISTANCE; METABOLIC SYNDROME; PLASMA; SERUM;
D O I
10.1373/clinchem.2008.112425
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Adiponectin is an adipocyte-derived hormone circulating in different multimer complexes. The high-molecular-weight (HMW) complex is likely the active form of this protein and has been recognized as a risk marker for type 2 diabetes and coronary artery disease (CAD). Because quantification of HMW adiponectin by Western blot analysis is time-consuming, novel ELISAs have been developed to simplify measurements in clinical research. However, these enzyme immunoassays have not been cross-validated in larger patient groups. We evaluated 2 individual ELISA systems by comparison to Western blotting for measurement of the distribution of HMW adiponectin in healthy individuals and patients with CAD and type 2 diabetes. METHODS: We measured HMW adiponectin in 204 individuals (83 CAD patients, 81 type 2 diabetes patients, and 40 healthy controls). Correlations, range of agreement, and imprecision of HMW concentrations obtained using 2 commercial ELISAs (#1, ALPCO Diagnostics; #2, Millipore) were evaluated by comparison with quantitative Western blotting. RESULT: Adiponectin results of the ELISAs were significantly correlated with those obtained by Western blotting (both r > 0.75, P < 0.001). Deming regression and Bland-Altman analyses indicated high agreement among the 3 immunoassays. The median difference between HMW adiponectin concentrations measured by ELISA and by Western blot was +0.4 mg/L for ELISA #1 and -0.4 mg/L for ELISA #2 with 95% of value differences < 3 mg/L. CONCLUSIONS: Selective measurement of HMW adiponectin by ELISA is feasible; however, individual differences among immunoassays must be considered. The evaluated ELISAs exhibit analytical characteristics that allow their use as equivalent for Western blot analysis in larger clinical and epidemiological groups.
引用
收藏
页码:568 / 572
页数:5
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