BNP -381T/C and 1551G/A polymorphisms were associated with circulating NT-proBNP levels (P=0.018) but did not predict prevalent diabetic nephropathy or mortality in type 1 diabetic patients.
Observational (n=380)
380 type 1 diabetic patients with and without diabetic nephropathy followed for a median of 12.6 years.
BNP gene polymorphisms (-381T/C and 1551G/A) vs Different genotypes (TT vs TC vs CC)
Prevalent diabetic nephropathy, circulating NT-proBNP levels, and all-cause or cardiovascular mortality, p=0.018
p-value: p=0.018
BACKGROUND: Circulating N-terminal pro-brain natriuretic peptide (NT-proBNP) levels are elevated in patients with diabetic nephropathy and independently predict excess cardiovascular morbidity and mortality. Therefore, we investigated the association between two polymorphisms -381T/C and 1551G/A of the BNP gene, plasma NT-proBNP levels and mortality prognosis in 380 type 1 diabetic patients with and without diabetic nephropathy. METHODS: In a prospective observational follow-up study, 197 type 1 diabetic patients with diabetic nephropathy 121 men, age mean (SD) 41 +/- 9. 5 years, duration of diabetes 28 +/- 8. 0 years, glomerular filtration rate 67 +/- 28 ml/min/1. 73 m2, and a matched control group of 183 patients with longstanding type 1 diabetes and persistent normoalbuminuria (111 men, age 43 +/- 10. 0 years, duration of diabetes 27 +/- 8. 3 years) were followed for 12. 6 (0. 0-12. 9) years. Plasma NT-proBNP concentration was determined by immunoassay at baseline. The BNP genotypes were determined by TaqMan chemistry based assays. RESULTS: The two polymorphisms were in almost complete linkage disequilibrium (r2 = 0. 883) and thus only the results of the -381T/C promoter polymorphism are shown. There was no significant difference between cases and controls in either genotype distributions (cases TT 32%, TC 53%, CC 15%; controls TT 28%, TC 52%, CC 20%) or allele frequencies (cases T/C 0. 58/0. 42; controls T/C 0. 54/0. 46) for the -381T/C polymorphism. Among the 164 normoalbuminuric patients without antihypertensive treatment and previous major cardiovascular disease (CVD), the -381T/C polymorphism was associated with circulating levels of NT-proBNP median (interquartile range) 21 (5-32), 34 (12-67) and 32 (12-58) ng/l for TT, TC and CC, respectively (P = 0. 041) persisting after adjustment for covariates (P = 0. 018). During follow-up, the -381T/C polymorphism did not predict all-cause or cardiovascular mortality among type 1 diabetic patients with or without diabetic nephropathy. CONCLUSIONS: The BNP -381T/C and 1551G/A polymorphisms are associated with circulating levels of NT-proBNP but not with prevalent overt diabetic nephropathy. These polymorphisms do not predict all-cause or cardiovascular mortality in Caucasian type 1 diabetic patients with or without diabetic nephropathy.
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Maria Lajer
Boehringer Ingelheim (Denmark)
Lise Tarnow
Heart Failure & Transplant
Anders Jorsal
Regional Hospital Horsens
Nephrology Dialysis Transplantation
Rigshospitalet
Steno Diabetes Centers
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Lajer et al. (Tue,) conducted a observational in Type 1 diabetes with and without diabetic nephropathy (n=380). BNP gene polymorphisms (-381T/C and 1551G/A) vs. Different genotypes (TT vs TC vs CC) was evaluated on Prevalent diabetic nephropathy, circulating NT-proBNP levels, and all-cause or cardiovascular mortality (p=0.018). BNP -381T/C and 1551G/A polymorphisms were associated with circulating NT-proBNP levels (P=0.018) but did not predict prevalent diabetic nephropathy or mortality in type 1 diabetic patients.
synapsesocial.com/papers/6a20e889e2d1a39857ecc412 — DOI: https://doi.org/10.1093/ndt/gfm360
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