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临床试验/NCT02470455
NCT02470455已完成不适用

Effect of Atorvastatin on Glycemic Control in Prediabetic Patients

Shri Ramachandra Bhanj Medical College1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2011年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
75
试验地点
1
主要终点
Change in Glycosylated Hemoglobin (HbA1c) from baseline

研究概览

简要总结

The study was conducted to find out any possible effect of Atorvastatin on glycemic parameters in prediabetic patients.

详细描述

Diabetes is a growing public health problem throughout the world, threatening global health and economic prosperity. Currently, approximately 171 to 194 million people in the world have diabetes, the majority of the cases being Type II. This number is expected to increase to more than 330 million by the year 2025-a record doubling within a single generation. India with 62.2 million diabetic patients is fast becoming the diabetes capital of the world with possibility of the number of diabetic patients reaching the 80 million mark by 2030. Every sixth diabetic in the world is an Indian. China with 43.2 million patients comes second, followed by the US where 26.8 million people suffer from the disease.

This spectacular increase in the frequency of Type II diabetes is being paralleled by a similarly alarming increase in obesity, which is one of the major risk factors for Type II diabetes. Because of the close linkage of these two conditions, Ziv and Shafrir have suggested the term "diabesity" to describe this association. This dual epidemic which was largely ignored by the public health community until recently has come as a great surprise involving enormous economic burden as well as in terms of health. Disorders of glucose metabolism are associated with increased risk for cardiovascular disease (CVD) complications, including coronary, peripheral and cerebral arterial disease, that account for the majority of morbidity and mortality among patients with diabetes mellitus (DM).

Type II diabetes is commonly associated with dyslipidaemia, which represents a synergistic risk factor for cardiovascular disease. The National Cholesterol Education Program Adult Treatment Panel III (ATP III) listed diabetes as a coronary heart disease (CHD) risk equivalent for setting therapeutic goals for LDL cholesterol. A goal for LDL cholesterol of <100 mg/dl was recommended for patients with CHD and CHD risk equivalents. For the majority of patients with diabetes, this LDL cholesterol goal would evoke the use of cholesterol-lowering drugs, particularly statins. Some Interventional studies emphasized that statin treatment leads to a reduction in cardiovascular events independent of lipid reduction with possible benefits for patients with Type II diabetes. Statins could also contribute to diabetes prevention owing to lipid-lowering and so-called pleiotropic action. Statins improve endothelial function, inhibit smooth muscle cell proliferation, and reduce oxidative stress and inflammation. Thus, with recent FDA approved indications for statins being widened, statins are currently amongst the most widely used drugs in patients with or without diabetes.

Although statin therapy reduces cardiovascular risk, its relationship with the development of diabetes is controversial. Retrospective analysis of the West of Scotland Coronary Prevention Study (WOSCOPS) revealed that 5 years of treatment with pravastatin reduced diabetes incidence by 30%. The authors suggested that although lowering of triglyceride levels could influence diabetes incidence, other mechanisms such as anti-inflammatory action may be involved. On the contrary, pravastatin did not decrease diabetes incidence in another trial including glucose-intolerant humans, suggesting that early inception of statin therapy may be required for effective diabetes prevention. Likewise, simvastatin did not affect diabetes incidence in patients with atherosclerosis in the Heart Protection Study. In contrast, atorvastatin marginally increased diabetes incidence in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT-LLA), which could be explained by statistical variation.

A recent review of 13 studies by Naveed Sattar, et al. published in The Lancet in 2010, on statins and their side-effects including a total of more than 91,140 participants suggested that use of statins is associated with increased risk of Type II diabetes by 9%.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any patient on statins therapy whose blood sugar level is within normal limit.
  • Pre-diabetic patients (IFG and/or IGT) on statins
  • Patients who agreed to participate in the study and signed the informed consent form without any external motivation

排除标准

  • Diagnosed cases of DM, both type I and II, on different anti-diabetic regimen
  • Patients on β-blockers, thiazide diuretics, corticosteroids, which can affect blood sugar level
  • Pregnancy and lactation
  • Co-existing or other organ involvement like kidney, liver which can affect blood sugar level

研究组 & 干预措施

Normoglycemic group

25 patients were recruited who were on Atorvastatin and with normal blood glucose and Hb1Ac level.

干预措施: Atorvastatin (Drug)

Prediabetic with normal GTT

25 patients were recruited who were on Atorvastatin and with fasting blood sugar level 100-125 mg/dl with normal GTT.

干预措施: Atorvastatin (Drug)

Prediabetic with impaired GTT

25 patients were recruited who were on Atorvastatin and with fasting blood sugar level 100-125 mg/dl with impaired GTT.

干预措施: Atorvastatin (Drug)

结局指标

主要结局

Change in Glycosylated Hemoglobin (HbA1c) from baseline

时间窗: At baseline and at 6 monhts, 12 months and 18 months follow up

次要结局

  • Lipid profile(At baseline)
  • Change in Fasting blood sugar from baseline(At baseline and at 6 monhts, 12 months and 18 months follow up)
  • Change in Post prandial blood sugar from baseline(At baseline and at 6 monhts, 12 months and 18 months follow up)

研究者

发起方
Shri Ramachandra Bhanj Medical College
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Sansita Parida

Resident

Shri Ramachandra Bhanj Medical College

研究点 (1)

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