TY - JOUR
T1 - Sulfonylurea therapy is associated with increased NT-proBNP levels in the treatment of type 2 diabetes
AU - Tildesley, Hugh D.
AU - Aydin, Cristina M.
AU - Ignaszewski, Andrew
AU - Strelzow, Jason A.
AU - Yu, Eugenia
AU - Bondy, Greg
PY - 2007/2/14
Y1 - 2007/2/14
N2 - Background: We sought to determine N-terminal pro-Brain Natriuretic Peptide (NTproBNP) levels among a population of individuals with type 2 diabetes, and to correlate these levels with diabetes medications and patient demographics. Methods: We analyzed data from 506 patients with type 2 diabetes. We compared NT-proBNP levels of these patients with those from the general population. We also sought to determine whether patients' NT-proBNP levels were correlated with diabetes medications, age, gender, creatinine, hemoglobin A1C levels, BMI, blood pressure, and lipid levels. Results: Increasing doses of sulfonylureas were associated with increasing levels of NT-proBNP. However, patients on combined sulfonylurea and metformin therapy had lower NT-proBNP levels than those on sulfonylureas alone. Neither thiazolidinediones nor insulin were associated with NT-proBNP levels. The majority of patients with type 2 diabetes had similar NT-proBNP levels compared to a reference group from the general population. In no age category did NT-proBNP levels differ significantly between men and women. Levels of NT-proBNP were positively associated with age (p < 0.0001), systolic blood pressure (p < 0.01) and creatinine levels (p < 0.0001), and negatively associated with diastolic blood pressure (p < 0.001). Levels of NT-proBNP were not associated with A1C, BMI, triglycerides, and high density lipoprotein (p = NS). Conclusions: Levels of NT-proBNP are associated with increasing sulfonylurea dosage, age, blood pressure, and creatinine levels. There is unlikely to be clinically significant differences in NT-proBNP levels between patients with type 2 diabetes and a normal population.
AB - Background: We sought to determine N-terminal pro-Brain Natriuretic Peptide (NTproBNP) levels among a population of individuals with type 2 diabetes, and to correlate these levels with diabetes medications and patient demographics. Methods: We analyzed data from 506 patients with type 2 diabetes. We compared NT-proBNP levels of these patients with those from the general population. We also sought to determine whether patients' NT-proBNP levels were correlated with diabetes medications, age, gender, creatinine, hemoglobin A1C levels, BMI, blood pressure, and lipid levels. Results: Increasing doses of sulfonylureas were associated with increasing levels of NT-proBNP. However, patients on combined sulfonylurea and metformin therapy had lower NT-proBNP levels than those on sulfonylureas alone. Neither thiazolidinediones nor insulin were associated with NT-proBNP levels. The majority of patients with type 2 diabetes had similar NT-proBNP levels compared to a reference group from the general population. In no age category did NT-proBNP levels differ significantly between men and women. Levels of NT-proBNP were positively associated with age (p < 0.0001), systolic blood pressure (p < 0.01) and creatinine levels (p < 0.0001), and negatively associated with diastolic blood pressure (p < 0.001). Levels of NT-proBNP were not associated with A1C, BMI, triglycerides, and high density lipoprotein (p = NS). Conclusions: Levels of NT-proBNP are associated with increasing sulfonylurea dosage, age, blood pressure, and creatinine levels. There is unlikely to be clinically significant differences in NT-proBNP levels between patients with type 2 diabetes and a normal population.
KW - Cardiovascular disease
KW - N-terminal pro-Brain Natriuretic Peptide
KW - Sulfonylurea therapy
KW - Type 2 diabetes
UR - http://www.scopus.com/inward/record.url?scp=33846593286&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2006.03.014
DO - 10.1016/j.ijcard.2006.03.014
M3 - Article
C2 - 16824633
AN - SCOPUS:33846593286
SN - 0167-5273
VL - 115
SP - 312
EP - 317
JO - International Journal of Cardiology
JF - International Journal of Cardiology
IS - 3
ER -