磺脲类药物对糖尿病患者冠心病转归的影响。

Acta medica Hungarica Pub Date : 1992-01-01
G Pogatsa, M Z Koltai, G Jermendy, J Simon, Z Aranyi, G Ballagi-Pordany
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引用次数: 0

摘要

对1040例糖尿病患者进行回顾性研究。第一代磺脲类药物(n = 227)在首次心绞痛发作(5 +/- 1年,平均+/- S.E.)或急性心肌梗死(6 +/- 1年)后的生存时间明显(P < 0.001)短于格列本脲治疗(n = 144)、单独治疗(n = 282)或胰岛素治疗(n = 387)的患者(9 +/- 1年)。第一代磺脲类药物患者的收缩压(166 +/- 1/91 +/- 1mmhg)高于格列本脲治疗(159 +/- 1/91 +/- 1mmhg)或单独治疗(155 +/- 1/89 +/- 1mmhg)或胰岛素治疗(156 +/- 1/89 +/- 1mmhg)的患者(P < 0.01)。两种磺胺脲类药物组血清钠水平(138 +/- 1 mmol/l)均低于其他组(143 +/- 1 mmol/l) (P < 0.05)。在观察期间,576名患者死亡,其中412人死于心血管或肾功能衰竭。在合并冠心病的糖尿病患者中,除收缩压升高外,其他危险因素无显著差异。第一代磺脲类药物治疗患者的生存时间较短,可能与第一代磺脲类药物的致心律失常活性有关。在调查期间,治疗的改善、代谢和心血管的改变并不是第一代磺脲类药物治疗患者生存时间缩短的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of sulphonylurea therapy on the outcome of coronary heart diseases in diabetic patients.

A retrospective study was performed on 1040 diabetic patients. The survival time of those treated with first generation sulphonylureas (n = 227) was considerably (P < 0.001) shorter after the first attack of angina pectoris (5 +/- 1 years, mean +/- S.E.) or acute myocardial infarction (6 +/- 1 years) than of those (9 +/- 1 years) on glibenclamide treatment (n = 144), with regime alone (n = 282) or treated with insulin (n = 387). The systolic blood pressure of patients with first generation sulphonylureas (166 +/- 1/91 +/- 1 mmHg) proved to be higher (P < 0.01) than those treated with glibenclamide (159 +/- 1/91 +/- 1 mmHg) or being on regime alone (155 +/- 1/89 +/- 1 mmHg) or on insulin (156 +/- 1/89 +/- 1 mmHg) treatments. Serum sodium level was found to be lower (P < 0.05) in patients treated with any kind of sulphonylureas (138 +/- 1 mmol/l) than in the other patients (143 +/- 1 mmol/l). During an observation period, 576 of patients died, 412 of them due to cardiovascular or renal failures. Among the diabetic subjects suffering from coronary heart disease no difference could be detected in risk factors except for higher systolic blood pressure. The shorter survival time of patients treated with first-generation sulphonylureas might be explained by the arrhythmogenic activity of first-generation sulphonylureas. Improvement in therapy, metabolic and cardiovascular alterations during the survey can not be responsible for the shorter survival time of patients treated with first generation-sulphonylureas.

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