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Asia Pacific J Clin Nutr (1993) 2, 191-194

Preferred meal patterns in non-insulin-dependent diabetes

Mark L. Wahlqvist MD, FRACP, Richard W. Simpson DM, FRACP, Che Sam Lo MD, PhD and Pauline Cooper MSc, Grad Dip Diet

Department of Medicine, Monash Medical Centre, Monash University, Melbourne, Victoria, Australia

Current advice on the across-the-day distribution of energy and carbohydrate intakes in non-insulin-dependent diabetes (NIDD) is based on inadequate evidence. We have addressed this by a comparison of an even as opposed to a main evening meal pattern in 11 subjects with NIDD. Contributions of macronutrients to energy intake were fat 29%, protein 20% and carbohydrate 51% with each meal pattern. The peak glycaemic response in the morning was not as good as the response in the evening (P<0.01), where an even energy and carbohydrate spread was used; this contrasts with previous reports in healthy subjects where the morning response to glucose is better than that later in the day. This difference between peak morning and peak evening glycaemic response was not seen with a main evening meal. There was a lower overall glycaemic response with a main evening meal compared with an even meal pattern (P<0.01, by area comparison). The overall insulin response was not significantly different between the two meal patterns, although the sensitivity for insulin appeared better in the evening where there was an evening main meal.


Introduction

Most contemporary nutritional advice for those with non-insulin-dependent diabetes (NIDD) is given on the basis that patients should be spared excessive quantities of carbohydrate on any one eating occasion1. This has been even more consequential as efforts have been made to increase the proportion of energy from carbohydrate in the diabetic diet2,3.

However, in most western food cultures, there is a main meal, often in the evening, and a change from this pattern can be socially disruptive. Despite the fact that 24 hour glucose and insulin profiles have been well described in healthy subjects4 and in diabetes, it is by no means certain that those with NIDD are advantaged in their glycaemic control by avoidance of a main evening meal in favour of a more even spread of carbohydrate over the day. We have studied a group of subjects with NIDD with two different meal patterns in order to resolve this question.

Methods

Subjects

Studies were performed after an overnight fast with only water to drink. The two meal studies were separated by two weeks. Non-insulin-dependent diabetics were selected for this study. All but one, who was on glibenclamide, were managed by diet alone. Each subject gave informed consent. Apart from diabetes, those recruited were in good health. Their characteristics are shown in Table 1. One subject was on digoxin and frusemide to control cardiac failure on the basis of ischaemic heart disease.

Table 1. Characteristics of 11 subjects (4 men and 7 women NIDD).

Subjects Age(years) BMI Kg.m-2 BP (mmHg) Years since diagnosis of diabetes
Men (n=4) 63.8± 5.0 25.4± 0.5 92.5± 3.2 3.9± 0.6
women (n=7) 70.0+3.5 28.1+1.1 102 ± 1.1 6.4± 0.8

One person, a woman, took her usual 2.5 mg glibenclamide at the commencement of breakfast. (1) The number of subjects is shown in parentheses (2) The Mean ± SE are shown (3) BMI = Body Mass Index (4) BP = the geometric mean blood pressure (= Systolic BP+2 Diastolic BP/3)

Meals

We devised two meal patterns, an even and main evening meal, whose energy distribution is shown in Table 2. Total energy was provided on the basis of 20 calories (82KJ) per kg body weight. We devised meals or snacks so that the macronutrient composition was fat 29%, protein 20% and carbohydrate 51%. The carbohydrate was principally from unrefined sources being wholemeal bread, fruit and vegetables, with up to 10% of total energy as added sucrose. In this study, no leguminous vegetables were used. The protein came principally from lean lamb, but bread and small quantities of cheddar cheese also contributed.

Table 2. Distribution of energy intake (%) during 24 hours with an 'even' meal distribution or a main evening meal eating pattern.

Meal Even Main evening meal
Breakfast 27 14
Mid-morning 6 6
Lunch 27 14
Mid-afternoon 6 6
Evening 27 40
Supper 7 20
Total 100 100

Time for each subject to ingest a particular meal or snacks was the same, within 5 minutes, for each meal pattern.

Breakfast was at 08.45, mid-morning snack at 10.00, lunch at 12.00, mid-afternoon snack at 15.00, evening meal at 18.00 and supper at 20.30 hours. Where blood glucose or plasma insulin response areas were calculated, they were those from the commencement of one eating episode to the commencement of the next or, for supper, to the conclusion of the study at 21.30 hours.

Analytical methods

Blood glucose was measured by a glucose oxidase method5. The CV was 2.3% at 18.4 mmol. L-1 n=44. Plasma insulin was measured by radioimmunoassay6. The CV was 5.0% at 10-100 m u.ml-1 n=10.

Statistical method

Paired t-tests were the basis of comparison between meal patterns of particular points in the day where blood glucose or plasma insulin were measured or where areas under the response curves were compared. Area was calculated according to the rule of polygons. Peak glycaemic and insulin responses in the morning and evening were also compared using paired t-tests.

Results

The blood glucose profiles from 08.30 to 21.30 hours for 11 diabetic subjects are shown in Figure 1. The commencement of the six eating occasions of (three meals and three snacks) are indicated by arrowheads. With an even meal distribution, blood glucose concentration was i significantly higher in the morning and lower in the evening than with a main evening meal. The total blood glucose response (calculated as area) was greater with an even meal distribution than with a main evening meal (Table 3).

Figure 1. Comparison of blood glucose profiles in NIDDM: Even vs Main Evening meal patterns.

Table 3. Comparison of glucose area (mmol.l-1 min) between 'even' meal and main evening meal eating pattern.

  n Even meal Main evening meal
Fasting 11 8.3± 0.8 8.8± 1.0
Breakfast 11 47.5± 5.2 45.8± 5.1
Mid-morning 11 38.8± 5.9* 33.3± 4.5
Lunch 11 80.0± 11.1* 69.4± 10.4
Mid-afternoon 11 47.6± 7.1** 40.5± 6.0
Evening 11 61.1± 3.5 64.8± 6.2
Supper 11 11.6± 1.4 12.4± 1.4
Total 11 285.2± 35.5** 264.2± 32.7

(1) n=the number of subjects (2) The mean ± SE are shown (3) The significant differences between 'Even meal' and 'Main evening meal' patterns is indicated by *P<0.05 and **P<0.01.

The peak glycaemic response in the morning was greater than in the evening with an even meal pattern (P<0.01), but there was no significant difference in these glycaemic responses with a main evening meal (see Figure 1).

Apart from the evening at 20.30 hours when plasma insulin was greater with an even meal pattern than a main evening meal (Figure 2), there were no significant differences in insulin responses (Table 4). However, the peak insulin responses in the morning were less than the evening (P<0.05) for the even meal pattern, but the reverse (P<0.05) for the main evening meal pattern.

Figure 2. Comparison of blood insulin profiles in NIDDM: Even vs Main Evening meal patterns.

Table 4. Comparison of insulin area (pmol .1 - 1 min) between 'even' meal and main evening meal eating pattern.

  n Even meal Main evening meal
Fasting 11 66± 13 63± 10
Breakfast 11 690± 106 745± 158
Mid-morning 11 597± 101 988± 264
Lunch 11 1259± 163 1450± 158
Mid-afternoon 11 642± 123 604± 286
Evening 11 1358± 298 1051± 177
Supper 11 356± 83 243± 40
Total 11 4971± 804 5511± 1177

(1) n=the number of subjects (2) The mean ± SE are shown (3) There were no significant differences between 'Even meal' and 'Main evening meal' patterns (P<0.05).

Discussion

Diurnal variation in blood glucose

In healthy subjects, glucose tolerance is better earlier than later in the day7 with an even meal distribution, in the non-insulin diabetics studied, the reverse is the case. However, a main evening meal restores the pattern of blood glucose towards that of healthy subjects. On the day of the study subjects had a low fat intake with the carbohydrate mainly unrefined, it may not be possible to extrapolate our findings to other macronutrient profiles.

Relative values of even versus main evening meal pattern

Morning hyperglycaemic is often a problem in the management of non-insulin-dependent diabetes. From our findings, it would seem possible to improve the morning situation, without overall reduction in glycaemic control, by a move towards a main evening meal pattern. The total glycaemic profile by area was significantly less with a main evening meal than with an even meal pattern, although the full extent of this difference over 24 hours is difficult to judge as the study finished at 21.30 hours.

For many people, especially those with an AngloCeltic food and work culture, there is a social advantage in a main evening meal which, for those with diabetes, will be preferred as well. Further consideration also needs to be given to whether the maintenance of a main evening meal pattern long-term would be as beneficial as it appears, in the present study, after changes to it in a single day.

Insulin responses to different meal patterns

The total insulin response, by area, was not significantly different between the two meal patterns. Thus, the improved overall glycaemic control with main evening meal was not at the expense of hyperinsulinaemia. Indeed, plasma insulin was actually greater in the evening with an even meal as opposed to a main evening meal pattern.

Hyperinsulinaemia is said to be adverse for macrovascular disease8, blood glucose is more important than plasma insulin in the determination of arterial compliance9. Whether blood glucose or plasma insulin is regarded as important for macrovascular disease, the main evening meal pattern would still be acceptable. If, in the event that we have measured mainly pro-insulin, as suggested by a recent UK study10, our findings may not represent an increase in insulin sensitivity in the evening with a main meal pattern, but a changing pattern of proinsulin to insulin conversion.

References

  1. Wahlqvist, ML. Diet in the treatment of diabetes. Med J Aust 1980; 2:64-68.
  2. Wahlqvist ML. Dietary fibre and carbohydrate metabolism. Am J Clin Nutr 1987; 45:1232-1236.
  3. Mann J. Diabetic dietary prescriptions. Brit Med J 1989; 298:1535-1536.
  4. Tasaka Y, Sekine M, Wakatsuki M, Ohgawasa H and Shizume K. Levels of pancreatic glucagon, insulin, and glucose during twenty-four hours of the day in normal subjects. Horm Metab Res 1975; 7:205-206.
  5. Spencer WW, Sylvester D and Nelson GH. Evaluation of glucose method in which a hydrogen perioxide electrode is used. Clin Chem 1978; 24:386-388.
  6. Albano JDM, Ekins RP, Maritz G and Turner RC. A sensitive, precise radioimmuno-assay of serum insulin relying on charcoal separation of bound and free hormone moieties. Acta Endocrinologica, 1972; 70:487-496.
  7. Carroll KF and Nestel PJ. Diurnal variation in glucose tolerance and insulin secretion in man. Diabetes 1973; 22:333-348.
  8. Walhqvist ML, Relf JRN, Myers KA and Lo CS. Diabetes and macrovascular disease: risk factors for atherogenesis and non-invasive investigation of arterial disease. Human Nutr Clin Nutr 1984; 38C: 175-184.
  9. Wahlqvist ML. Lo CS, Myers KA, Simpson RW and Simpson JM. Putative determinants of arterial wall compliance in NIDDM. Diabetes Care 1988; 11:787-790.
  10. Temple RC, Carrington CA, Luzio SD, Owens DR, Schneider AE, Sobey WJ and Hales CN: Insulin deficiency in non-insulin-dependent diabetes. Lancet 1989: 293 295.


Copyright © 1993 [Asia Pacific Journal of Clinical Nutrition]. All rights reserved.

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