2004
DOI: 10.1007/s00125-004-1410-y
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Response to Chiasson et al.: Acarbose for the prevention of Type 2 diabetes, hypertension and cardiovascular disease in subjects with impaired glucose tolerance: facts and interpretations concerning the critical analysis of the STOP-NIDDM Trial data

Abstract: authors received honoraria from Bayer. However, withholding this information in the publication of results [3,4] and declaring that there was no conflict of interest [3] is misleading.In conclusion, both the STOP-NIDDM Trial and the meta-analysis of selected studies with acarbose are seriously flawed and no valid conclusions can be drawn from the published data.

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Cited by 14 publications
(4 citation statements)
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“…Acarbose was reported to reduce cardiovascular events in a secondary analysis of the STOP-NIDDM trial, 7 but with only 47 participants having the outcome in question this could be a chance finding. 19 The lack of any substantial benefit on cardiovascular events in ACE compared with STOP- 21 Nateglinide, a rapid-acting insulin secretagogue which reduces postprandial hyperglycemia by increasing circulating insulin levels, was evaluated in the Nateglinide And Valsartan in Impaired Glucose Tolerance Outcomes Research (NAVIGATOR) trial. In patients at high cardiovascular disease risk and with impaired glucose tolerance followed for median 5•0 years, nateglinide 120 mg once daily showed no effect on the risk of cardiovascular events and a 7% significant increased risk for new-onset diabetes.…”
Section: Discussionmentioning
confidence: 99%
“…Acarbose was reported to reduce cardiovascular events in a secondary analysis of the STOP-NIDDM trial, 7 but with only 47 participants having the outcome in question this could be a chance finding. 19 The lack of any substantial benefit on cardiovascular events in ACE compared with STOP- 21 Nateglinide, a rapid-acting insulin secretagogue which reduces postprandial hyperglycemia by increasing circulating insulin levels, was evaluated in the Nateglinide And Valsartan in Impaired Glucose Tolerance Outcomes Research (NAVIGATOR) trial. In patients at high cardiovascular disease risk and with impaired glucose tolerance followed for median 5•0 years, nateglinide 120 mg once daily showed no effect on the risk of cardiovascular events and a 7% significant increased risk for new-onset diabetes.…”
Section: Discussionmentioning
confidence: 99%
“…After a mean follow-up of 3.3 years, the acarbose-treated group achieved 25 % and 36% RR reduction based on one or two OGTTs in progression to diabetes compared with placebo. The effect of acarbose was observed across all ages, at all BMIs, and in both sexes, while there was some evidence of an accompanying improvement in CVD risks [255][256][257].…”
Section: Antiobesity Treatmentmentioning
confidence: 87%
“…9 However, the small number of cardiovascular events in that study, challenges the validity of the observations, and criticisms of the study execution, end point definition and data reporting have been debated. [10][11][12] No long-term data from the DPP are presently available. Moreover, the risk of developing DM after discontinuing either medical regimen remains unknown.…”
Section: Introductionmentioning
confidence: 99%