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African Journal of Biomedical Research
Ibadan Biomedical Communications Group
ISSN: 1119-5096
Vol. 11, Num. 2, 2008, pp. 161-172
TOXICOSIS OF NON-STEROIDAL ANTI-INFLAMMATORY AGENTS IN RATS

African Journal of Biomedical Research, Vol. 11, No. 2, May, 2008, pp. 161-172

Full Length Research Article

Anthropometric and Biochemical Profiles of Black South African Women  

1Hattingh Z, 2Walsh C.M, 3Veldman F.J, 4Bester C.J, 5Oguntibeju O.O  

1School of Tourism, Hospitality and Sport, Central University of Technology, Free State; 2Department of Nutrition and Dietetics, University of the Free State;
 3School of Health Technology, Central University of Technology, Free State; 4Department of Biostatistics, University of the Free State;
Department of Biomedical Sciences, Faculty of Health & Wellness Sciences, Cape Peninsula University of Technology, Bellville, South Africa
*Author for correspondence:Tel: +17584546128, Fax:+17584546811, Email: bejufemi@yahoo.co.uk

Received: March 2008
Accepted (Revised): May 2008
Published: May 2008

Code Number: md08022

ABSTRACT

It has been reported that the diet of rural women in most African countries differs considerably from that of their urban counterparts, with the urban diet composed of more refined carbohydrates and fatty food. This study examines anthropometric and biochemical profiles and the association between these parameters in pre-menopausal, post-pubertal black South African women. A representative sample of 500 participants, randomly selected in Mangaung, Bloemfontein in the Free State Province, using township maps obtained from the Bloemfontein Municipality were recruited to participate.  Younger women were aged 25-34 years and older women 35-44 years. Anthropometric and biochemical profiles were determined according to standard methods.  From the original sample of 500 women, 496 were eligible to participate.  Of the younger women 30.1% and of the older women 27.7% were overweight, while 23.3% of younger women and 24% of older women had a body mass index (BMI) ³30 kg/m2, indicating obesity.  Most women had a waist-hip ratio (WHR) <0.8, indicating gynoid fat distribution.  The majority of women from both age groups had a body fat percentage >25% (92.5% and 94% respectively of younger and older women).  Of the younger women 6.8% and of the older women 13.8% had triglyceride (TG) levels higher than the reference range.  Total cholesterol levels fell within the reference range for 79.8% of the younger women and 71.3% of the older women. Glucose and insulin levels were within reference ranges for most women of both age groups. A significant association was found between insulin sensitivity and BMI and between insulin sensitivity and TG levels in both age groups. No significant association was found between waist circumference and elevated glucose levels in both age groups. A significant difference between insulin sensitivity and WHR was observed in the older group of women.  The prevalence of overweight and obesity reported in this population may pose a potential risk for the development of chronic diseases such as type 2 diabetes. 

Keywords: Black women, anthropometric indicators, biochemical parameters, obesity, type 2 diabetes mellitus

INTRODUCTION 

The universal movement of concurrent changes in dietary structure and physical activity patterns, referred to as “the nutrition transition”, is reflected in nutritional outcomes, including changes in body composition.  These shifts coincide with major conversions in the general health profile (Popkin, 2006) of especially middle- and lower-income communities (Kim et al., 2000).

With the nutrition transition, populations tend to move away from traditional food practices towards the consumption of diets higher in energy (Compher, 2006), more diverse diets, and the consumption of more refined grains, saturated fat and sugar (Popkin, 1994).  Literature indicates that South African and other population groups who formed part of the nutrition transition have become increasingly vulnerable to developing chronic diseases (Compher, 2006; Steyn et al., 1997; Drewnowski & Popkin, 1997; Temple et al., 2001; Macintyre et al., 2002) such as obesity, type 2 diabetes mellitus, and cardiovascular disease.  Albertse, Neethling and De Villiers (1990) reported that the diet of rural Zulu women in South Africa differs considerably from that of urban Zulu women, with the rural diet composed of 69% carbohydrates, 17% fat, 13% protein and 37 g of fibre per day, compared with 50% carbohydrates, 31% fat, 16% protein and 14 g of fibre in the daily diet of urban Zulu women.  This places urban black South African women at higher risk for developing obesity and type 2 diabetes mellitus or other chronic diseases – hence the urgent need to assess the anthropometric and biochemical profile of South African women living in Mangaung, the urban black township of Bloemfontein in the Free State Province.

SUBJECTS AND METHODS 

Population and sampling: A representative sample of 500 women from two formal settlements (Phahameng and Botchabela) and two informal settlements (Joe Slovo and Namibia) in Mangaung, the black residential township of Bloemfontein (capital city of the Free State Province), was randomly selected to participate in the study. 

Post-pubertal but pre-menopausal black women were randomly selected from the two age groups 25-34 and 35-44 years using township maps.  The residential plots in the four selected areas were counted and numbered.  Namibia consisted of 2 995 plots, Pahameng 1 711, Joe Slovo 1 359, and Botchabela 2 308.  A proportionate number of respondents were randomly selected from these settlements.  Twenty subjects were recruited per week over a 25-week period (March 2000 – November 2000).  A randomly selected residence was approached by a trained community healthcare worker.  One woman per selected residence was screened for eligibility.  If nobody was home, the residence to the right was targeted and, if still unsuccessful, the residence to the left of the original address was approached.  If all attempts failed, another plot was randomly selected.  The assigned community health workers explained the purpose of the study to possible participants.  The women took part voluntarily, after giving written informed consent.  The informed consent document was approved by the Ethics Committee of the Faculty of Health Sciences, University of the Free State (ETOVS no. 02/00).

Respondents fasted overnight, abstained from exercise, and avoided consuming alcohol and caffeine for 24 hours prior to anthropometric measurement and the collection of blood samples.  All blood samples were taken in the morning. Three interpreters were available to assist researchers where language problems were encountered. Each participant was examined by a medical practitioner.

Anthropometric measurements: Anthropometric measurements were performed by a qualified anthropometrist.  Weight was determined with a “Seca” digital electronic scale, to the nearest 0.1 kg, with the participant dressed in light clothing.  Height, determined with a stadiometer to the nearest 0.1 cm, body mass index (BMI) calculated from body weight and height in metres squared, and waist-hip ratio (WHR) calculated from waist circumference and hip circumference were determined according to standard methods (Lee & Nieman, 1996; Hammond, 2000).  Bioelectrical impedance analysis was used to determine body composition for fat (Bodystat, 2000) according to cut-off points (Smolin & Grosvenor, 2003).

Blood sampling and analysis: Blood samples from the participants, who had fasted overnight, were collected by a qualified nursing sister and were used to determine fasting triglycerides (TGs), fasting total cholesterol, fasting serum albumin, fasting serum glucose and fasting serum insulin levels.  Ten millilitres of whole blood were left to clot at room temperature.  These samples were centrifuged at 3 360 rpm for 20 minutes to allow the serum to separate.  Serum samples were frozen at –72ºC in EppendorfR vials for later analysis.  Fasting TGs were determined using the GPO-PAP method, total cholesterol using the CHOD-PAP method, serum albumin using a colorimetric endpoint method, and glucose using an enzymatic colorimetric method (supplied by Roche Diagnostics, GmbH, Mannheim, Germany).  Serum insulin was determined by the DRG insulin ELISA, a solid-phase two-site enzyme immunoassay. Insulin sensitivity was calculated using the formula: 10 000/(glucose x insulin) (Donahue et al., 1988).

Statistical analysis

The data was categorised into the age groups 25-34 years and 35-44 years.  For each group, medians or percentiles were described by applying continuous variables. Categorical variables were described using percentages.  BMI, WHR and fat percentage were calculated and categorised according to the cut-off points. For each group, the categorised variables were described using percentages. The association between waist circumference and glucose levels was determined as described by Newcombe (1998).  The association between BMI and TG levels was determined by Spearman rank order correlations.

RESULTS 

From the original sample of 500 women, 496 women qualified to participate. Of those who qualified, 279 were aged 25-34 years and 217 were aged 35-44 years.  Four women were found to be pregnant during the medical examination and were excluded from the study. 

Anthropometric indicators: BMI values of both age groups are presented in Table 1. More than half of the women in both age groups had a BMI ³25 kg/m2.  More women in the younger group had a BMI within the reference value. In the younger group 30.1% of women were overweight, while 27.7% of the older women were overweight.  Twenty-three percent of the younger women and 24% of the older women had a BMI ³30 kg/m2, indicating obesity.

The WHR of both age groups is presented in Table 2.   Most women in both age groups had a WHR below 0.8, indicating gynoid fat distribution.  Of the younger women 83.5% had a WHR below 0.8%, while this applied to 62.7% of the older women. The majority of subjects had a fat percentage higher than the recommended range of 20-25% (92.5% of the younger group and 94% of the older group) (Table 3). 

Table 1: BMI of the two age groups (25-34 and 35-44 years)

Age group

BMI category (kg/m2)

<18.5

18.5<20

20<25

25<30

≥30

25-34 years

N

%

N

%

N

%

N

%

N

%

7

2.5

14

5

109

39.1

84

30.1

65

23.3

35-44 years

N

%

N

%

N

%

N

%

N

%

9

4.1

17

7.8

79

36.4

60

27.7

52

24

Key: <18.5 kg/m2 (underweight), 18.5<20 kg/m2 (lower weight), 20<25 kg/m2 (normal weight), 25<30 kg/m2 (overweight), ≥30 kg/m2 (obese)

Biochemical parameters

Of the younger group 93.2% and of the older group 86.2% had fasting TG levels within the normal value (<2 mmol/l), while 6.8% of the younger women and 13.8% of the older women had TG levels ³2 mmol/l.  Fasting cholesterol levels fell within the reference value (>0.9<5.2 mmol/l) for 79.8% of younger women and 71.3% of older women, while 15.9% of younger women and 27.8% of older women fell within the moderate risk group (5.2<7.8 mmol/l).  On the whole, the percentage of women in the high-risk category (≥7.8 mmol/l) for cholesterol was relatively low (4.3% of younger women and 0.9% of older women).  A higher percentage of women in both groups (98.6% of younger women and 99.5% of older women) had normal (34-48 g/l) serum albumin levels.  Fasting serum glucose levels were within the reference range (3.05 - 6.38 mmol/l) for most women in the two age groups (84.1% of younger women and 89.9% of older women).  More women in the younger group than in the older group demonstrated high fasting serum glucose levels (10.5% and 4.2% respectively).  Results showed that the majority of women had serum insulin levels within the reference range (<25mU/ml). Results of the biochemical parameters indicated that most women in the two age groups had fasting TG, albumin, glucose and insulin levels within reference ranges.

The 25 percentile (Q1), 50 percentile (median-Q2) and 75 percentile (Q3) values of biochemical parameters of the two age groups of women are presented in Table 4 and Table 5.

Associations between fasting glucose and waist circumference, BMI and TG, insulin sensitivity and BMI, and insulin sensitivity and TG were determined.  No significant associations were found between waist circumference and fasting glucose (Table 6) and between TG and BMI in both groups (Table 7). For insulin sensitivity (25-34 age group), the number of women in each group ranged from 68 in group 1 to 69 in groups 2, 3 and 4. In group 1, with the lowest insulin sensitivity (highest insulin resistance), the median BMI was 27.6 kg/m2.  As insulin sensitivity improved, the median BMI decreased (groups 1 to 4). Group 4, the most insulin-sensitive group (lowest insulin resistance), reported the lowest median BMI (23 kg/m2).  When the medians of BMI were compared between all groups by 95% non-parametric confidence interval (CI), significant differences were found between BMI and insulin sensitivity of groups 1 and 4, groups 2 and 4, and groups 3 and 4 (Table 8).

Table 2: WHR of the two age groups (25-34 and 35-44 years)

Age group

WHR

<0.8

≥0.8

25-34 years

N

%

N

%

233

83.5

46

16.5

35-44 years

N

%

N

%

136

62.7

81

37.3

Table 3: Fat percentage of the two age groups (25-34 and 35-44 years)

Age group

<20%

20≤25%

>25%

25-34 years

N

%

N

%

N

%

3

1.1

18

6.5

258

92.5

35-44 years

N

%

N

%

N

%

3

1.4

10

4.6

204

94

Key: <20% (low fat percentage), 20≤25% (normal fat percentage), >25% (high fat percentage)

Table 4: Biochemical parameters of age group 25-34 years

Biochemical parameters                          

Age group 25-34 years

N

Q1

Q2

Q3

Fasting blood glucose (mmol/l)

276

3.9

4.3

4.7

Serum insulin µU/ml

276

3.0

7.0

15.5

Insulin sensitivity

275

144.5

325.3

755.3

Total cholesterol (mmol/l)

277

3.6

4.2

4.9

TG (mmol/l)

277

0.7

0.9

1.2

Albumin (g/l)

277

38.8

41.3

44.3

Key: Q1 (25 percentile), Q2 (50 percentile), Q3 (75 percentile)

Table 5: Biochemical parameters of age group 35-44 years

Biochemical parameters

Age group 35-44 years                        

N

Q1

Q2

Q3

Fasting blood glucose (mmol/l)

217

4

4.4

4.9

Serum insulin µU/ml

217

2.5

6.3

10.7

Insulin sensitivity

217

206

390.4

977.5

Total cholesterol (mmol/l)

216

3.9

4.5

5.3

TG (mmol/l)

216

0.8

1.1

1.5

Albumin (g/l)                       

215

38.9

41.5

43.6

Key: Q1 (25 percentile), Q2 (50 percentile), Q3 (75 percentile)

Table 6: Association between fasting glucose and waist circumference

Parameter

<35 years

≥35 years

No & %

No & %

Waist circumference <0.88 cm & glucose >normal

 

21 (72.4)

 

5 (55.6)

Waist circumference ≥0.88 cm & glucose >normal

 

5 (27.6)

 

4 (44.4)

95% CI for difference between %

(-3.67; 17.5)*

(-2.7; 11.6)*

*Insignificant difference between fasting glucose and waist circumference

In the age group 35-44 years, the number of subjects in each group ranged from 53 in group 2 and 54 in group 3, to 55 in groups 1 and 4.  In group 1, with the lowest insulin sensitivity, the median BMI was 26.2 kg/m2 while in group 4, the most insulin-sensitive group, the median BMI was 23.5 kg/m2. Significant differences were found between BMI and insulin sensitivity of groups 1 and 4, groups 2 and 4, and groups 3 and 4 (Table 9).  

Table 7: Association between BMI and TG

BMI category

<35 years

≥35 years

Normal TG

High TG

Normal TG

High TG

BMI<18.5

6(85.7%)

1(14.3%)

9(100%)

0(0%)

BMI 18.5<25

118(97.5%)

3(2.5)

85(88.5%)

11(11.5%)

BMI 25<30

77(93.9%)

5(6.1%)

50(83.3%)

10(16.7)

BMI ≥30

57(89.1%)

7(10.9%)

43(82.7%)

9(17.3%)

*Insignificant difference

When the medians of WHR were compared between all insulin-sensitive groups by 95% non-parametric CI for the median difference, a significant difference was found between groups 1 and 4 of the older women (Table 11). When the medians of TG were compared with all insulin-sensitive groups, a significant difference was found between groups 1 and 3 and between groups 1 and 4 within the age group 25-34 years (Table 12).

Table 8: Association between BMI and insulin sensitivity in age group 25-34 years

Parameter

Insulin sens 1

12.13≤144.47

Insulin sens 2

>144.47≤325.28

Insulin sens 3

>325.28≤755.34

Insulin sens 4

>755.34

BMI

68

69

69

69

Median

27.6

26.7

26.3

23.0

BMI

Median difference

95% non-parametric CI

Gp 1-2

Gp 1-3

Gp 1-4

Gp 2-3

Gp 2-4

Gp 3-4

0.5

0.6

3.5

0.1

3.1

2.9

-1.33; 2.28

-1.26; 2.48

1.91; 5.38*

-1.73; 1.87

1.40; 4.73*

1.41; 4.51*

*Values with the same symbol differ significantly between groups

  •    Sens= sensitivity
  •    Gp=(group)

Table 9: Association between BMI and insulin sensitivity in age group 35-44 years

Parameter

Insulin sens 1

14.10≤206.01

Insulin sens 2

>206.01≤309.39

Insulin sens 3

>309.39≤977.52

Insulin sens 4

>977.52

BMI (No)

55

53

54

55

Median

26.2

26

26.5

23.5

BMI

Median difference

95% non-parametric CI

Gp 1-2

Gp 1-3

Gp 1-4

Gp 2-3

Gp 2-4

Gp 3-4

0.6

-0.1

3.2

-0.4

2.8

3.3

-1.80; 2.87

-2.20; 2.23

1.24; 5.27*

-2.81; 1.60

0.79; 4.88*

1.60; 5.24*

*Values with the same symbol differ significantly between groups
Gp=group                              Sens=sensitivity

Table 10: Association between WHR and insulin sensitivity in age group 25-34 years

Parameter

Insulin sens 1

12.13≤144.47

Insulin sens 2

>144.47≤325.28

Insulin sens 3

>325.28≤755.34

Insulin sens 4

>755.34

WHR

No

68

69

69

69

Median

0.74

0.73

0.74

0.74

WHR

Median difference

95% non-parametric CI

Gp 1-2

Gp 1-3

Gp 1-4

Gp 2-3

Gp 2-4

Gp 3-4

0.002

0.02

0.01

0.01

0.01

-0.002

-0.02; 0.03

-0.01; 0.04

-0.01; 0.03

-0.02; 0.04

-0.01; 0.02

-0.02; 0.02

Gp=group                              Sens=sensitivity

Table 11: Association between WHR and insulin sensitivity in age group 35-44 years

Parameter

Insulin sens 1

14.10≤206.01

Insulin sens 2

>206.01≤390.39

Insulin sens 3

>390.39≤977.52

Insulin sens 4

>977.52

WHR

No

55

53

54

55

Median

0.79

0.78

0.77

0.76

WHR

Median difference

95% non-parametric CI

Gp 1-2

Gp 1-3

Gp 1-4

Gp 2-3

Gp 2-4

Gp 3-4

0.002

0.02

0.03

0.01

0.01

-0.002

-0.01; 0.04

-0.001; 0.05

0.001; 0.06*

-0.02; 0.04

-0.01; 0.04

-0.02; 0.03

*Values with the same symbol differ significantly between groups

Gp=group                              Sens=sensitivity

Table 12: Association between TG and insulin sensitivity in age group 25-34 years

Parameter

Insulin sens 1

12.13≤144.47

Insulin sens 2

>144.47≤325.28

Insulin sens 3

>325.28≤755.34

Insulin sens 4

>755.34

TG

No

68

69

69

69

Median

1.1

0.92

0.83

0.91

TG

Median difference

95% non-parametric CI

Gp 1-2

Gp 1-3

Gp 1-4

Gp 2-3

Gp 2-4

Gp 3-4

0.1

0.2

0.2

0.1

0.02

-0.05

-0.01; 0.3

0.06; 0.39*

0.01; 0.32*

-0.05; 0.2

-0.11; 0.1

-0.2; 0.1

*Values with the same symbol differ significantly between groups

Gp=group
Sens=sensitivity

Table 13: Association between TG and insulin sensitivity in age group 35-44 years

Parameter

Insulin sens 1

14.10≤206.01

Insulin sens 2

>206.01≤390.39

Insulin sens 3

>390.39≤977.52

Insulin sens 4

>977.52

TG

No

55

52

54

55

Median

1.3

0.98

1.1

1.1

TG

Median difference

95% non-parametric CI

Gp 1-2

Gp 1-3

Gp 1-4

Gp 2-3

Gp 2-4

Gp 3-4

0.22

0.14

0.2

-0.1

-0.01

0.06

0.03; 0.4*

-0.06; 0.34

0.02; 0.40*

-0.3; 0.1

-0.1; 0.2

-0.1; 0.2

*Values with the same symbol differ significantly between groups
Gp=group                              Sens=sensitivity

Within the age group 35-44 years, when the medians of TG were compared with those of all insulin-sensitive groups, a significant difference was found between groups 1 and 2 and between groups 1 and 4 (Table 13). Significant associations between insulin sensitivity and BMI and between insulin sensitivity and TG levels were found in this population.  No associations were found between fasting glucose levels and waist circumference. The association between insulin sensitivity and WHR in the age group 25-34 years was not significant.

DISCUSSION

Urbanisation and lower physical activity levels, amongst other things, are associated with the increasing prevalence rates of obesity in Southern Africa (Walker et al., 2001), probably explaining the noticeable prevalence of overweight and obesity in the studied population.  About 50% of all women demonstrated a BMI ³25 kg/m2, with 30.1% of younger women and 27.7% of older women falling into the overweight category.  Results from South African studies conducted in recent years have indicated relatively high prevalence rates of overweight and obesity, particularly in the black population. The South African Demographic and Health Survey, a national cross-sectional study conducted in rural and urban areas in the nine provinces, revealed that 29.2% of male participants and 56.6% of female participants were overweight or obese.  Of the black women, 31.8% were obese, 26.7% were overweight and 43.4% had abdominal obesity (Puoane et al., 2002).  In a study conducted in a partly rural and urban black area in the Free State Province, South Africa, prevalence rates of obesity in this population ranged between 27.5% and 49% for women in QwaQwa (partially rural area) and between 31.1% and 54.3% for women in Mangaung (urban area).  The authors of that survey warned that urgent measures were necessary to prevent an epidemic of atherosclerotic disease in the black population (Mollentze et al., 1995).  Although the results from the present study indicated lower prevalence rates of obesity than the last-mentioned study, the percentage of women falling into the overweight category should be a matter of concern, as overweight may eventually lead to obesity and might pose a potential risk for developing type 2 diabetes or cardiovascular diseases. In the Transition and Health during Urbanisation of South Africans (THUSA) study conducted among black women living in the North West Province of South Africa, 25.2% of subjects were overweight and 28.6% were obese.  BMI also correlated significantly with diastolic blood pressure, serum triacylglycerols, fasting glucose and log fasting insulin (Kruger et al., 2001). 

In this study, most women in both age groups had a WHR below 0.8. This value may increase if the respondents in this study do not control their dietary intake and increase their levels of physical activity.  Mollentze et al., 1995) noted that a subgroup of obese persons with central or android obesity is at greater risk of developing cardiovascular disease.  Results of WHR in this study  (mean WHR of 0.74 in the younger group and 0.78 in the older group) were lower than the mean WHR of women in both populations studied by the last-mentioned authors, and for all age groups, which exceeded 0.8 [18], indicating a greater risk of developing cardiovascular disease and type 2 diabetes.  Another study conducted among urban blacks in Cape Town showed a mean WHR of 0.8 for women older than 30 years (Levitt et al., 1993).  A mean WHR of 0.8 for healthy, obese white and black South African women, with no significant differences found between these groups and between diabetic white and diabetic black women, was also reported previously (Van der Merwe et al., 1999).  For individual respondents with a high WHR, an increase in physical activity could possibly have a favourable effect on body fat distribution, resulting in a reduction in the WHR and lower body obesity.

A matter of concern is the total number of women who demonstrated a significantly high body fat percentage. Regardless of weight, almost all the women that participated in this study had a fat percentage higher than the recommended value. Results from the present study show that the levels of physical activity in women were very low, coupled with the consumption of a high-energy diet and high macronutrient intake (Hattingh et al., 2006).  Exercise in itself may not produce major weight losses, but exercise along with regulated dietary intake and lifestyle could help to alter the body composition favourably, reducing fat and increasing muscle mass (Caterson, 1998).

In this study, most of the women in the two age groups had normal fasting TG levels, but the higher percentage of older women with increased fasting TG levels calls for constant evaluation and monitoring. It has been shown that increased TG levels are associated with diet, alcohol consumption, obesity, and underlying or untreated diabetes mellitus, while weight loss, a low-saturated-fat or low-cholesterol diet, increased physical activity, smoking cessation and restricted alcohol use could assist in lowering high TG levels Krummel, 2000).

A large percentage of women showed fasting cholesterol levels within the reference range. However, about 28% of the older women fell in the moderate risk group.  It has been found that total cholesterol concentrations in blacks increase with age (Kruger et al., 2001), possibly explaining the 28% of older women falling into the moderate risk group for increased total cholesterol in the present study.   However, mean cholesterol and saturated fat intakes in an earlier study of ours (Hattingh et al., 2006) also exceeded recommendations, and could possibly contribute to this. Total cholesterol levels in the study by Mollentze et al. (1995) indicated that urban participants had a greater tendency towards higher cholesterol levels than rural participants.  Increased cholesterol levels are usually associated with a diet high in saturated fat and animal products. The large number of subjects in the moderate risk group was also a disturbing factor in the study of Mollentze et al. (1995), as is the case in this study.

For most women in the two age groups, fasting blood glucose levels fell within the reference range. Of the younger women 10.5% and of the older women 4.2% had blood glucose levels above the reference level. Raised blood glucose levels are commonly associated with the risk of developing type 2 diabetes.  It is known that in some population groups, there has been an increase in the prevalence of type 2 diabetes associated with either migration or a rapid change from a traditional lifestyle to one characterised by increased consumption of energy-dense foods high in fat and sugars, as well as reduced levels of physical activity (Mann, 1998).  A study investigating the prevalence of type 2 diabetes among urban blacks in the greater Cape Town area found a 7% prevalence rate of impaired glucose tolerance and an 8% prevalence rate of type 2 diabetes after being age adjusted (Levitt et al., 1993).  Results from a study to determine the prevalence of type 2 diabetes and risk factors in Mamre, a peri-urban area near Cape Town composed primarily of descendants of the Khoi people (an indigenous population of South Africa), indicated an age-adjusted prevalence rate of 10.8% for type 2 diabetes and 10.2% for impaired glucose tolerance.  The authors concluded that potentially modifiable risk factors included upper-segment fat distribution and physical inactivity (Levitt et al., 1999).  In the study by Mollentze et al. (1995) the prevalence rates of type 2 diabetes were 6% (Mangaung) and 4.8% (QwaQwa) and were more frequently observed in men >45 years and in women >35 years. The fact that younger women in our study had been living in an urban area for a mean of 15 years and older women for a mean of 19 years indicates that urbanisation could possibly have had an influence on the glucose profiles of those women with high glucose levels.  However, factors such as obesity, age and physical inactivity could also have played a role in this regard.  In particular, the higher percentage of younger women with increased glucose levels possibly shows that the younger urbanised women had to a greater extent adopted a more Westernised diet than their older counterparts.  Insulin resistance refers to an impaired biologic response to either exogenous or endogenous insulin. Both insulin resistance and insulin deficiencies are usual causes of type 2 diabetes (Franz, 2000).  Glucose is the major regulator of insulin secretion, and the pancreas is sensitive to changes in glucose at physiological concentrations.  In individuals with normal glucose tolerance, fasting plasma glucose levels are maintained by a complex interaction between hepatic glucose disposal and peripheral tissue glucose uptake.  Downward regulation of plasma glucose entirely depends on circulating plasma insulin that enhances the uptake of glucose by the peripheral tissues.  Impaired glucose tolerance, characterised by fasting hyperglycaemia, is largely due to increased glucagon secretion and the inability of the beta cells to secrete sufficient insulin, but is partly due to insulin resistance (Makuyana et al., 1999).  In this study, 12% of younger women and 10.6% of older women had insulin levels greater than the reference value. The implication is that these groups of women are more likely to present with insulin resistance.  For the women with high insulin levels, both genetic and lifestyle factors may play a role (Franz, 2000)although our study and other South African studies have tended to favour lifestyle factors. Intake of excessive kilojoules, physical inactivity and obesity are believed to increase insulin resistance (Franz, 2000), and all these have been documented in black South African women.

The association between anthropometric and biochemical profiles is discussed in the subsequent section. The use of waist circumference has been suggested as a good indicator of fasting blood glucose (Okosun et al., 1998). Obese black women with a waist measurement ≥0.88 cm are considered to be at higher risk of developing chronic diseases (James, 2001). In this study, however, no significant association between waist circumference and elevated glucose levels was observed.  The small percentage of women with elevated glucose levels makes statistical analysis of data difficult.  Also, no significant association was reported between TG levels and BMI. 

In black women, obesity is characterised by a decrease in insulin sensitivity and lower pancreatic beta cell function, probably explaining the increased prevalence of type 2 diabetes mellitus in these South Africans (Van der Merwe et al., 2000). An association between BMI and insulin sensitivity was observed in our study, with respondents within the two age groups with the lowest insulin sensitivity also having the highest mean BMI, while insulin sensitivity improved as BMI decreased. A reduction in BMI per se could therefore have beneficial effects on the health of these black women, regardless of fat distribution.  High intakes of dietary fats may decrease insulin sensitivity in individuals already at increased risk for insulin resistance due to obesity and a sedentary lifestyle (Mayer-Davis et al., 1997).

It has been suggested that WHR circumference is a significant predictor of plasma TG, glucose and insulin concentrations and that it is correlated positively with an in vivo index of insulin resistance (Evans et al., 1984). A significant difference between WHR and insulin sensitivity was found in the insulin sensitivity of groups 1 and 4 of the older women.  In the younger women, WHR showed no significant association with insulin sensitivity.  Insulin is the major determinant and stimulant of lipoprotein lipase, an enzyme system responsible for the peripheral catabolism of triglyceride-rich lipoproteins.  It is likely that the enhancement of insulin sensitivity would lead to a more efficient lipolytic system with a consequent decrease in the TG concentration of the individual (Donahue et al., 1988). It is suggested that an increase in physical activity can have beneficial effects on the TG profile and insulin sensitivity (Mayer-Davis et al., 1997) of the women who participated in this study.

Conclusion

The prevalence of overweight in the studied population was high.  Although the prevalence of obesity in this study was lower than the rate reported in some other studies, the percentage of women who are overweight is a matter of concern, as a BMI ≥25 kg/m2 is associated with adverse health consequences. The association between insulin sensitivity and BMI indicates that a large proportion of women are at risk of developing hyperinsulineamia as their BMI increases, which in turn could enhance the risk for obesity and type 2 diabetes. It is believed that the prevalence of overweight, obesity and high body fat percentage reported in this population may be associated with a diet that is high in energy and fat content and which may pose a risk for the development of cardiovascular diseases.

Acknowledgements

The National Research Foundation is acknowledged for financial support of this study.  The authors would like to thank the women who participated in the study, the community health workers for contacting the sample, and the research team who collected the data.

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