Literature DB >> 15857159

Relationship among urinary albumin excretion rate, lipoprotein lipase PvuII polymorphism and plasma fibrinogen in type 2 diabetic patients.

M Javorský1, M Kozárová, J Salagovic, I Tkáč.   

Abstract

Plasma fibrinogen level represents a strong cardiovascular risk factor and is regulated by an interplay of genetic and environmental factors. Hyperfibrinogenemia frequently occurs in cluster with dyslipidemia within the frame of insulin resistance syndrome (IRS) and type 2 diabetes mellitus. Genetic variants with a pleiotropic effect have been proposed to cause IRS features including hyperfibrinogenemia. We studied the influence of polymorphisms in lipoprotein lipase (LPL) gene, beta-fibrinogen gene (FIBB) and environmental factors on plasma fibrinogen levels in type 2 diabetes patients. 131 type 2 diabetes patients (mean age 62+/-10 years, 33% male) were genotyped for polymorphisms in LPL gene (intron 6 PvuII, intron 8 HindIII) and FIBB gene (-148C/T, -455G/A) by PCR-RFLP method. Fibrinogen was measured by thrombin coagulation method, albuminuria by immunoturbidimetric assay. Polymorphism LPL PvuII showed a gene-dose effect on fibrinogen levels, with the highest fibrinogen in P-P- homozygotes (p = 0.05, analysis of variance). P-carriers (P-P- and P+P- combined) had significantly higher fibrinogen levels compared with P+P+ homozygotes (3.74+/-1.40 g/l vs 3.06+/-1.20 g/l, p=0.03). Other studied polymorphisms were not significantly related to fibrinogen levels. Age- and sex-adjusted fibrinogenemia correlated significantly with albuminuria (r = 0.48, p=0.001), serum uric acid (r = 0.42, p=0.006) and serum creatinine (r = 0.32, p=0.04). Multiple stepwise linear regression identified interaction term of LPL PvuII and albuminuria as an independent predictor of fibrinogen level, explaining 18% of fibrinogen variance. Albuminuria thus appears to be the best predictor of fibrinogen plasma levels in type 2 diabetic patients. Relationship between albuminuria and fibrinogenemia may be modified by the genotype LPL PvuII, which also shows a weak association with plasma fibrinogen level in type 2 diabetes patients.

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Year:  2005        PMID: 15857159     DOI: 10.33549/physiolres.930704

Source DB:  PubMed          Journal:  Physiol Res        ISSN: 0862-8408            Impact factor:   1.881


  3 in total

1.  The association of lipoprotein lipase PvuII polymorphism and niacin intake in the prevalence of metabolic syndrome: a KMSRI-Seoul study.

Authors:  Eunjung Shin; Na-Young Park; Yangsoo Jang; Hyunhee Oh; Jayoung Jeong; Yunsook Lim; Myoungsook Lee
Journal:  Genes Nutr       Date:  2011-10-29       Impact factor: 5.523

2.  Association of lipoprotein lipase (LPL) single nucleotide polymorphisms with type 2 diabetes mellitus.

Authors:  Yoon Shin Cho; Min Jin Go; Hye Ree Han; Seung Hun Cha; Hung Tae Kim; Haesook Min; Hyoung Doo Shin; Chan Park; Bok Ghee Han; Nam Han Cho; Chol Shin; Kuchan Kimm; Bermseok Oh
Journal:  Exp Mol Med       Date:  2008-10-31       Impact factor: 8.718

3.  Quantile-specific heritability of plasma fibrinogen concentrations.

Authors:  Paul T Williams
Journal:  PLoS One       Date:  2022-01-07       Impact factor: 3.240

  3 in total

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