| Literature DB >> 26411958 |
Amir Emadian1, Rob C Andrews2, Clare Y England3, Victoria Wallace4, Janice L Thompson1.
Abstract
Weight loss is crucial for treating type 2 diabetes mellitus (T2DM). It remains unclear which dietary intervention is best for optimising glycaemic control, or whether weight loss itself is the main reason behind observed improvements. The objective of this study was to assess the effects of various dietary interventions on glycaemic control in overweight and obese adults with T2DM when controlling for weight loss between dietary interventions. A systematic review of randomised controlled trials (RCT) was conducted. Electronic searches of Medline, Embase, Cinahl and Web of Science databases were conducted. Inclusion criteria included RCT with minimum 6 months duration, with participants having BMI≥25·0 kg/m2, a diagnosis of T2DM using HbA1c, and no statistically significant difference in mean weight loss at the end point of intervention between dietary arms. Results showed that eleven studies met the inclusion criteria. Only four RCT indicated the benefit of a particular dietary intervention over another in improving HbA1c levels, including the Mediterranean, vegan and low glycaemic index (GI) diets. However the findings from one of the four studies showing a significant benefit are questionable because of failure to control for diabetes medications and poor adherence to the prescribed diets. In conclusion there is currently insufficient evidence to suggest that any particular diet is superior in treating overweight and obese patients with T2DM. Although the Mediterranean, vegan and low-GI diets appear to be promising, further research that controls for weight loss and the effects of diabetes medications in larger samples is needed.Entities:
Keywords: ADA American Diabetes Association; Diet; GI glycaemic index; GL glycaemic load; LCM low carbohydrate Mediterranean; Systematic reviews; T2DM type 2 diabetes mellitus; Type 2 diabetes; Weight loss
Mesh:
Substances:
Year: 2015 PMID: 26411958 PMCID: PMC4657029 DOI: 10.1017/S0007114515003475
Source DB: PubMed Journal: Br J Nutr ISSN: 0007-1145 Impact factor: 3.718
Fig. 1Flow diagram showing the number of studies screened, assessed for eligibility, and included in the review.
Table summarising the results of changes in HbA1c from the eleven dietary interventions included in the systematic review (Mean values and standard deviations for mean weight loss and mean reduction HbA1c)
| HbA1c (%) at baseline | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| References | Participants | Mean |
| Intervention ( | Composition of prescribed diets | Mean weight loss (kg) | Mean decrease in HbA1c (%) | Duration | Attrition rate | Medication | Conclusion |
| Guldbrand | 61 overweight and obese adults with type 2 diabetes | 7·35 | LFD (31) | LFD: 55–60 % CHO, 10–15 % protein, 30 % fat LCD: 20 % CHO, 30 % protein, 50 % fat | 2·97 | −0·2 | 2 years | 9·7 % in LFD group and 13·3 % in LCD | Authors reported that at 6 months there
was a statistically significant difference in mean insulin dose in favour of
the LCD ( | No significant difference between dietary interventions in improving HbA1c | |
| Brehm | 124 overweight and obese adults with type 2 diabetes | 7·3 | High-MUFA diet (43) | MUFA: 45 % CHO, 15 % protein, 40 % fat (20 % MUFA) CHO: 60 % CHO, 15 % protein, 25 % fat | 4·0 ( | 0 | 12 months | 31 % for the MUFA group and 16 % for the HC group | Authors reported a lack of available information about participant’s drug usage. Only information on 32 participants’ drug use was available, which showed no systematic differences between diet groups. Therefore no adjustments were made for glucose-lowering medication | No significant difference between dietary interventions in improving HbA1c | |
| Fabricatore | 79 obese adults with type 2 diabetes | 6·8 | Low fat (39) | Low fat: <30 % fat Low GL: 3 or less servings of moderate-GL and 1 or less serving of high-GL foods/d | 4·5 ( | 0·1 ( | 40 weeks | 36·7 % | Authors stated that changes in HbA1c
were adjusted for medication use. Percentage of participants who increased,
decreased or did not change their diabetic medication regime did not differ
between the groups at week 20 ( | Low GL appears to be more effective in reducing HbA1c compared with a the LFD | |
| Elhayany | 259 overweight and obese adults with type 2 diabetes | 8·3 | LCMD (61) | LCM: 35 % low-GI CHO, 15–20 % protein, 45 % fat rich in MUFA TM: 50–55 % low-GI CHO, 15–20 % protein, 30 % fat rich in MUFA ADA: 50–55 % CHO, 15–20 % protein, 30 % fat | 10·1 | 2·0 | 12 months | 30·9 % | Authors do not mention baseline medication characteristics or any changes in glucose-lowering medication use during the course of the intervention | LCM diet appears to be more effective in reducing HbA1c compared with a TM and ADA diets | |
| Barnard | 99 obese adults with type 2 diabetes | 7·99 | Low-fat vegan diet (49)
| Low-fat vegan diet: 75 % CHO, 15 % protein, 10 % fat ADA: 60–70 % CHO, 15–20 % protein and MUFA | 4·4 ( | 0·34( | 74 weeks | 18·4 % for the vegan group 14 % for the ADA group | Net 74-week dosages were reduced in 35 % participants in vegan group and 20 % of those in the ADA group, and were increased in 14 % of vegan group and 24 % of conventional group | Once data are adjusted for medication use, there appears to be a significant benefit in the low-fat vegan diet in decreasing HbA1c compared with the ADA diet | |
| Esposito | 215 overweight adults with type 2 diabetes | 7·73 | LCMD (107) | LCMD: 50 % CHO, 20 % protein, no <30 % fat LFD: no >30 % fat with no >10 % SFA | 3·8 ( | 0·9 ( | 4 years | 9·3 % | After 4 years 44 % of participants in
the LCMD and 70 % of those in the LFD group required treatment (absolute
difference, −26·0 percentage points (95 % CI 0·51, 0·86), hazard ratio
adjusted for weight change, 0·70 (95 % CI 0·59, 0·90);
| LCMD appears to be more effective in reducing HbA1c compared with a LFD with less need for glucose-lowering medication | |
| Pedersen | 76 overweight adults with type 2 diabetes | 7·3 | HPD (21) | HPD: 40 % CHO, 30 % protein, 30 % fat SPD: 50 % CHO, 20 % protein, 30 % fat | 9·7 ( | 0·4 | 12 months | 40·8% | Did not account for changes in medication, although authors stated that 4 volunteers managed their diabetes with diet alone, and all others treated with oral medication and/or insulin | No significant difference between dietary interventions in improving HbA1c | |
| Iqbal | 144 obese adults with type 2 diabetes | 7·75 | LCD (40) | Low CHO: <30 g/d CHO Low fat: ≤30 % of energy for fat with <7 % of energy from SFA | 1·5 | 0·1 | 24 months | 60 % in the low-CHO group and 46 % in the low-fat group | Authors stated that many participants were unable to provide information regarding changes to medication or dosages and therefore the effects of glucose-lowering medication was not adjusted for | No significant difference between dietary interventions in improving HbA1c | |
| Ma | 40 overweight and obese adults with type 2 diabetes | 8·42 | ADA diet (21) | ADA: 60–70 % CHO, 15–20 % protein and 30 % fats Low GI: participants given goals to reduce daily dietary GI score to 55 | 0·80 | 0·43 | 12 months | 10 % for the ADA group and 10 % for the low-GI group | Participants in the low-GI group were
less likely to add or increase dosage of glucose-lowering medications (OR
0·26; | No significant difference between dietary interventions in improving HbA1c | |
| Milne | 70 overweight and obese adults with type 2 diabetes | 10·0 | 0·35 | Weight management diet (21)
| Weight management diet: restrict extrinsic simple sugars and energy dense foods, no advice for macronutrient contribution HC/fibre: 55 % CHO, 15 % protein, 30 % fat, 30 g or more dietary fibre/d Modified lipid diet: 45 % CHO, 19 % protein, 36 % fat | −1·5 | 0·1 | 18 months | 8·6 % | Authors state that 52·3 % of the weight management group, 57·1 % of the HC/fibre group and 50 % of the modified lipid diet were on glucose-lowering medication at baseline. However there is no mention of medication adjustments being made throughout the study | No significant difference between dietary interventions in improving HbA1c |
| Larsen | 99 overweight and obese adults with type 2 diabetes | 7·84 | HPD (53) | HP: 40 % CHO, 30 % protein, 30 % fat HC: 55 % CHO, 15 % protein, 30 % fat | 2·23 | 0·23 | 12 months | 9·2 % HP group | Authors reported a significant
reduction in the requirement for glucose-lowering medication in the HP group
compared with the HC group at 3 months ( | No significant difference between dietary interventions in improving HbA1c | |
LFD, low-fat diet; LCD, low carbohydrate diet; CHO, carbohydrate; HC, high carbohydrate; low GL, low glycaemic load; LCMD, low carbohydrate Mediterranean diet; TM, traditional Mediterranean; ADA, American Diabetes Association; LCM, low carbohydrate Mediterranean; GI, glycaemic index; TMD, traditional Mediterranean diet; HPD, high-protein diet; SPD, standard protein diet; HP, high protein.
Table summarising the changes in dietary intake at baseline and at end point of intervention
| References | Intervention ( | Dietary assessment tool used | Composition of prescribed diet | Composition of diet consumed | Comments |
|---|---|---|---|---|---|
| Guldbrand | LFD (31) | 3-d food record | LFD: 55–60 % CHO, 10–15 % protein, 30 % fat | LFD: 47 % CHO, 20 % protein, 31 % fat | There was a significant between group
differences for the percentage of energy from CHO, fat
( |
| LCD: 20 % CHO, 30 % protein, 50 % fat | LCD: 31 % CHO, 24 % protein, 44 % fat | ||||
| Brehm | High-MUFA diet (43) | 3-d food record | MUFA: 45 % CHO, 15 % protein, 40 % fat (20 % MUFA) | MUFA: 46 % CHO, 16 % protein, 38 % fat (20 % MUFA) | The high-MUFA-diet group consumed
significantly more total fat, PUFA and MUFA than the high-CHO group
( |
| CHO: 60 % CHO, 15 % protein, 25 % fat | CHO: 54 % CHO, 18 % protein, 28 % fat | ||||
| Fabricatore | Low fat (39) | 3-d food record | Low fat: <30 % fat | Low fat: 32·9 % fat GL 121·3 | Reductions in energy from fat were
significantly greater among those in the low-fat group at week 40
( |
| Low GL: 3 or less servings of moderate-GL and 1 or less serving of high-GL foods/d | Low GL: 39·8 % fat GL 88·6 | Low-GL group had significantly greater
reductions in energy from CHO ( | |||
| Changes on other measured dietary variable were not significantly different between groups | |||||
| Elhayany | LCM (61) | FFQ and 24-h recall | LCM: 35 % low-GI CHO, 15–20 % protein, 45 % fat rich in MUFA | No breakdown of the actual macronutrient content which was consumed during the intervention | Statistically significant trend in
percentage of energy from PUFA intake, highest 12·9 % for LCM, to 11·5 % in
TM, and lowest in ADA 11·2 % ( |
| TM: 50–55 % low-GI CHO, 15–20 % protein, 30 % fat rich in MUFA | Same significant trend observed for
MUFA fat intake (14·6, 12·8, and 12·6 % for LCM, TM and ADA, respectively,
| ||||
| ADA: 50–55 % CHO, 15–20 % protein, 30 % fat | Opposite trend seen for % of energy
from CHO, highest for ADA 45·4 % then 45·2 % for TM and lowest for the LCM
with 41·9 % ( | ||||
| Barnard | Low-fat vegan diet (49)
| 3-d food record | Low-fat vegan diet: 75 % CHO, 15 % protein, 10 % fat | Low-fat vegan diet: 66·3 % CHO, 14·8 % protein, 22·3 % fat | At the end point of intervention, dietary adherence was met by 51 % of participants in the vegan group and 48 % of those in the ADA group |
| ADA: 60–70 % CHO, 15–20 % protein and 30 % fats | ADA: 46·5 % CHO, 21·14 % protein and 33·7 % | ||||
| Esposito | LCMD (107) | Food diary records | LCMD: 50 % CHO, 20 % protein, no <30 % fat | LCMD: 44·2 % CHO, 18 % protein, 39·1 % fat, 10 % SFA, 17·6 % MUFA | Between group differences in % CHO and MUFA significantly different throughout the trial |
| LFD: no >30 % fat with no >10 % SFA | LFD: 51·8 % CHO, 17·9 % protein, 29·4 % fat, 9·4 % SFA, 12·4 % MUFA | ||||
| Pedersen | HPD (21) | FFQ and 24 h urea excretion | HPD: 40 % CHO, 30 % protein, 30 % fat | HPD: 39·2 % CHO, 26 % protein, 34·8 % fat | At 12 months adjusted urea excretion
was significantly different between groups (519 ( |
| SPD: 50 % CHO, 20 % protein, 30 % fat | SPD: 44·8 % CHO, 21·1 % protein, 34·0 % fat | ||||
| Iqbal | LCD (40) | 3-d food record | LCD: | LCD: 192·8 g/d CHO | Authors concluded that macronutrient intake was not significantly different between groups at any point. Authors concluded that both groups failed to achieve dietary targets |
| Low fat: ≤30 % of energy for fat with <7 % of energy from SFA | Low fat: 33·6 % of energy from fat | ||||
| Ma | ADA diet (21) | 7-d dietary recall | ADA: 60–70 % CHO, 15–20 % protein and 30 % fats | ADA: 38 % CHO, 80 GI, 20 % protein, 43 % fat | Differences in dietary GI did not reach
significance until 12 months ( |
| Low GI: participants given goals to reduce daily dietary GI score to 55 | Low GI: daily GI score of 76 37 % CHO, 76 GI, 20 % protein, 43 % fat | ||||
| Milne | Weight management diet (21)
| 24-h recall | Weight management diet: restrict extrinsic simple sugars and energy dense foods, no advice for macronutrient contribution | Weight management diet: 47·6 % CHO, 18·8 %, 33·6 %, 17·3 g dietary fibre/d | Authors concluded that almost none of the participants succeeded in achieving currently recommended intakes of either CHO or unsaturated fat |
| High CHO/fibre: 55 % CHO, 15 % protein, 30 % fat, 30 g or more dietary fibre/d | High CHO/fibre: 46·6 % CHO, 21·0 % protein, 32·4 % fat, 21·1 dietary fibre/d | ||||
| Modified lipid diet: 45 % CHO, 19 % protein, 36 % fat | Modified lipid diet: 46·4 % CHO, 19·7 % protein, 33·9 % fat | ||||
| Larsen | HPD (53) | 3-d food record | HPD: 40 % CHO, 30 % protein, 30 % fat | HPD: 41·8 % CHO, 26·5 % protein, 30·7 % fat | Significant differences between groups in the quantities of CHO and protein consumed |
| High CHO: 55 % CHO, 15 % protein, 30 % fat | High CHO: 48·2 % CHO, 18·9 % protein, 32·0 % fat |
LFD, low-fat diet; LCD, low carbohydrate diet; CHO, carbohydrate; low GL, low glycaemic load; GI, glycaemic index; LCM, low carbohydrate Mediterranean; TM, traditional Mediterranean; ADA, American Diabetes Association; LCMD, low carbohydrate Mediterranean diet; HPD, high-protein diet; SPD, standard protein diet.
Values are from reported dietary intakes at the end point of intervention.