Metabolic syndrome and mortality in stable coronary heart disease: relation to gender
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Metabolic syndrome and mortality in stable coronary heart disease: relation to gender. / Kragelund, Charlotte; Køber, Lars; Faber, Jens; Steffensen, Rolf; Hildebrandt, Per.
I: International Journal of Cardiology, Bind 121, Nr. 1, 2007, s. 62-7.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Metabolic syndrome and mortality in stable coronary heart disease: relation to gender
AU - Kragelund, Charlotte
AU - Køber, Lars
AU - Faber, Jens
AU - Steffensen, Rolf
AU - Hildebrandt, Per
N1 - Keywords: Aged; Coronary Angiography; Coronary Disease; Diabetes Mellitus; Female; Follow-Up Studies; Humans; Male; Metabolic Syndrome X; Middle Aged; Multivariate Analysis; Prospective Studies; Severity of Illness Index; Sex Factors
PY - 2007
Y1 - 2007
N2 - BACKGROUND: Metabolic syndrome (MS) is associated with subsequent development of type 2 diabetes and cardiovascular disease in the general population. The impact of MS on mortality in patients with stable coronary heart disease is less well defined, and the association of prognosis to gender is unknown. METHODS: 1041 patients with stable coronary heart disease, referred for elective coronary angiography were included in this study. At baseline, history of hypertension, body mass index, lipids, fasting plasma glucose, and insulin were recorded. All-cause mortality was determined after a median follow-up of 9.2 years. RESULTS: At follow-up 296 (28%) patients had died. 315 (30%) patients had MS based on the definition by the World Health Organization. Patients with MS more frequently had diabetes and three-vessel disease of the coronary arteries. Men had a more severe risk profile than women. In a multivariable Cox regression analysis, MS was not associated with excess mortality risk in the overall population [adjusted HR=1.3 (95% CI: 0.7-2.3), p=0.43]. In gender specific analyses MS increased risk of all-cause mortality in women [adjusted HR=2.2 (95% CI: 1.1-4.3), p=0.02], but not in men [adjusted HR=1.0 (95% CI: 0.5-1.9), p=0.93]. CONCLUSIONS: MS provides prognostic information in women, but not in men. This association was independent of conventional cardiovascular risk factors including previously unrecognised diabetes, and angiographic coronary artery disease.
AB - BACKGROUND: Metabolic syndrome (MS) is associated with subsequent development of type 2 diabetes and cardiovascular disease in the general population. The impact of MS on mortality in patients with stable coronary heart disease is less well defined, and the association of prognosis to gender is unknown. METHODS: 1041 patients with stable coronary heart disease, referred for elective coronary angiography were included in this study. At baseline, history of hypertension, body mass index, lipids, fasting plasma glucose, and insulin were recorded. All-cause mortality was determined after a median follow-up of 9.2 years. RESULTS: At follow-up 296 (28%) patients had died. 315 (30%) patients had MS based on the definition by the World Health Organization. Patients with MS more frequently had diabetes and three-vessel disease of the coronary arteries. Men had a more severe risk profile than women. In a multivariable Cox regression analysis, MS was not associated with excess mortality risk in the overall population [adjusted HR=1.3 (95% CI: 0.7-2.3), p=0.43]. In gender specific analyses MS increased risk of all-cause mortality in women [adjusted HR=2.2 (95% CI: 1.1-4.3), p=0.02], but not in men [adjusted HR=1.0 (95% CI: 0.5-1.9), p=0.93]. CONCLUSIONS: MS provides prognostic information in women, but not in men. This association was independent of conventional cardiovascular risk factors including previously unrecognised diabetes, and angiographic coronary artery disease.
U2 - 10.1016/j.ijcard.2007.04.068
DO - 10.1016/j.ijcard.2007.04.068
M3 - Journal article
C2 - 17566574
VL - 121
SP - 62
EP - 67
JO - International Journal of Cardiology
JF - International Journal of Cardiology
SN - 0167-5273
IS - 1
ER -
ID: 17395750