Associations of insulin-like growth factors, insulin-like growth factor binding proteins and acid-labile subunit with coronary heart disease

Summary objective  IGFs and their binding proteins (IGFBPs) are produced both systemically and locally by cells of the cardiovascular system. As growth promoters, they may play a role in atherosclerosis. design  Case–control, cross‐sectional. patients  A total of 95 nondiabetic male patients with co...

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Published inClinical endocrinology (Oxford) Vol. 61; no. 5; pp. 595 - 602
Main Authors Fischer, Frank, Schulte, Helmut, Mohan, Subburaman, Tataru, Mira-Christine, Köhler, Ekkehart, Assmann, Gerd, Von Eckardstein, Arnold
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.11.2004
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Summary:Summary objective  IGFs and their binding proteins (IGFBPs) are produced both systemically and locally by cells of the cardiovascular system. As growth promoters, they may play a role in atherosclerosis. design  Case–control, cross‐sectional. patients  A total of 95 nondiabetic male patients with coronary heart disease (CHD) and 92 probands from the Prospective Cardiovascular Münster (PROCAM) who were below the age of 60 years and matched by age, body mass index (BMI) and smoking habits measurements  We analysed the strength and independence of associations of angiographically assessed presence of CHD with BMI, systolic and diastolic blood pressure, total, high‐density lipoprotein (HDL) and LDL cholesterol, triglycerides, lipoprotein(a), apolipoproteins A‐I and B, total and free IGF‐I, IGF‐II, IGFBP‐1, IGFBP‐3, IGFBP‐5, acid‐labile subunit (ALS), insulin, C‐peptide, testosterone, DHEAS and sex hormone binding globulin. results  Using multivariate statistical analysis, the presence of CHD had significant positive associations with total IGF‐I, IGFBP‐5, ALS and IGFBP‐3. These associations were independent of each other as well as of traditional risk factors, insulin and sex hormones. conclusion  These observations may indicate a pathogenetic role of the GH/IGF axis in coronary atherosclerosis.
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ISSN:0300-0664
1365-2265
DOI:10.1111/j.1365-2265.2004.02136.x