Published in:
01-09-2008 | Article
A modified Mediterranean diet is associated with the greatest reduction in alanine aminotransferase levels in obese type 2 diabetes patients: results of a quasi-randomised controlled trial
Authors:
A. Fraser, R. Abel, D. A. Lawlor, D. Fraser, A. Elhayany
Published in:
Diabetologia
|
Issue 9/2008
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Abstract
Aim
The aim of the study was to compare the effect of different dietary interventions on alanine aminotransferase (ALT) in obese patients with diabetes.
Methods
A post hoc analysis of an open label, parallel design, quasi-randomised (allocation by alternation), controlled trial, conducted in Israel. Obese patients with diabetes (n = 259), treated in the community, were centrally allocated to one of three diets: (1) the 2003 recommended American Diabetes Association diet (ADA): 50–55% carbohydrate, 30% fat and 20% protein, n = 85; (2) a low glycaemic index (LGI) diet: 50–55% LGI carbohydrate, 30% fat, 15–20% protein, n = 89; or (3) a modified Mediterranean diet (MMD): 35% LGI carbohydrate, 45% fat that was high in monounsaturated fat, 15–20% protein, n = 85. ALT was measured at 6 and 12 months.
Results
ALT levels decreased in all arms; however, the MMD was associated with the lowest ALT levels at month 6 (n = 201: ADA n = 64, LGI n = 73, MMD n = 64) and month 12 of follow-up (n = 179). At 12 months mean ALT levels were 19.8 ± 1.4 U/l in the ADA diet arm (n = 54), 18.0 ± 1.5 U/l in the LGI diet arm (n = 64) and 14.4 ± 1.7 in the MMD arm (n = 61, p < 0.001). Evidence for an effect of diet on ALT levels persisted when controlling for post-randomisation changes in waist to hip ratio, BMI, homeostasis model assessment (HOMA) or triacylglycerol.
Conclusions
A Mediterranean diet may have a beneficial effect on liver steatosis in obese patients with diabetes. Results of trials assessing the effect of dietary composition on clinical outcomes should be awaited before a decisive conclusion can be reached. In addition to clinical outcomes, such studies should address the issue of primary prevention of steatosis in high-risk and healthy individuals.
Trial registration: ClinicalTrials.gov NCT00520182
Funding: This study was supported by a grant from Tnuva Research Institute, Rehovot, Israel.