Abstract
Background
Overweight and obesity are associated with health complications the gravity of which, vary with the regional deposition of the excess fat. The Body Mass Index (BMI) is often used to measure obesity although is an inferior predictor of cardiovascular disease risk mortality and morbidity compared with measures of abdominal obesity. We analyzed data from Uganda’s 2014 World Health Organization (WHO) STEPwise approach to surveillance of Non-communicable diseases (NCDs) survey to estimate the prevalence of abdominal obesity and associated factors to provide information on the prevention and control of overweight and obesity.
Methods
Data were collected using the WHO STEPS protocol. Waist measurement was taken using a non-stretchable standard tape measure mid-way between the lowest rib and iliac crest with the subject standing at the end of gentle expiration. Participants with waist circumference > 102 cm for men and 88 cm for women were classified as abdominally obese. We used weighted modified Poisson regression with robust error variance to estimate the prevalence of abdominal obesity and associated factors.
Results
Of the 3676 participants, 432 (11.8%) were abdominally obese; with the prevalence higher among females 412 (19.5%) compared with males 20 (1.3%). Compared with males, female participants were more likely to be abdominally obese Adjusted Prevalence Rate Ratio (APRR) 7.59 [5.58–10.33]. Participants who were married or cohabiting APRR 1.82 [1.29–2.57] and participants who were separated or divorced APRR 1.69 [1.17–2.46] were more likely to be abdominally obese compared with those who had never married before. Compared with rural dwellers, participants from urban areas were more likely to be abdominally obese APRR 1.29 [1.09–1.53]. Compared with participants with normal blood pressure, those with elevated blood pressure were more likely to be abdominally obese APRR 1.83 [1.57–2.14].Compared with participants without any education, those with secondary education were more likely to be abdominally obese APRR 1.42 [1.12–1.78].
Conclusions
There is a high prevalence of abdominal obesity among adults in Uganda which puts many at risk of developing associated metabolic complications. These data provide useful information for developing interventions and formulation of policies for the control and prevention of abdominal obesity in Uganda.
Keywords: Abdominal obesity, Non-communicable diseases, WHO STEPs methodology, Sub-Saharan Africa, Uganda
Background
The significance of obesity as a global public health challenge cannot be over emphasized. Cross country comparisons have shown steady increases in the prevalence of overweight and obesity in Africa which are envisaged to reach epidemic proportions in the near future if left unabated [1]. Between 1995 and 2011 the prevalence of overweight and obesity in Uganda increased more than 2-fold from 8 to 18.8% according to the Uganda Demographic Health Surveys (UDHS) [2, 3]. Overweight and obesity are associated with complications that include hypertension, atherosclerosis, diabetes and many types of cancers [4]. Aside from the degree of obesity, the regional distribution of fat is an important determinant of the health hazards associated with obesity. For example increased intra-abdominal fat has been associated with increased glucose intolerance [5], mortality from all causes, cardiovascular diseases and cancers [6]. The Body Mass Index (BMI) (kg/m2) is commonly used to quantify obesity and then classify individuals as underweight, normal weight, overweight or different subgroups of obesity. Although BMI has been shown to correlate well with measures of abdominal obesity at the population level, persons with higher readings of abdominal obesity will have more abdominal fat at any given BMI value at the individual level [7]. It has been shown that after adjusting for BMI, the risk of cardiovascular disease mortality is higher among persons with higher waist-circumference [6]. In fact, a meta analysis has shown that measures of abdominal obesity are superior to BMI in the detection of risk factors for cardiovascular diseases in both women and men [8].
Previously, there have not been any national population studies on obesity in Uganda. Some studies however have been conducted among young adults [9], adolescents [10], women and children [11], and some in selected districts representing urban and peri-urban settings [12]. Furthermore, all these studies used BMI as an indicator of obesity and therefore could not distinguish abdominal obesity from overall obesity.
In 2014, a nationwide survey was carried out in Uganda to provide baseline estimates of the major risk factors for Non-Communicable Diseases (NCDs). We analyzed data from this survey to estimate the prevalence of abdominal obesity and identify the associated factors to provide information for the prevention and control of abdominal obesity and its associated complications among adults in Uganda.
Methods
Study design
The Uganda national NCD risk factor survey was conducted using a cross-sectional study design. Data were collected using the World Health Organization’s (WHO) STEPwise approach to surveillance, a global standardized protocol for assessment of risk factors for NCDs [13]. A detailed description of the conduct, sampling procedures and methods used to conduct the survey has been described elsewhere [14–16]. Here we only describe the methods relevant to the content of this paper.
Measurements
Briefly, in STEP 1, the survey collected data on socio-demographic and behavioral characteristics including alcohol use, tobacco use, fruit and vegetable intake and level of physical activity (PA).
In STEP 2, physical measurements were made including weight, height, blood pressure, waist circumference and hip circumference. Three blood pressure readings were taken and the average of the last two was used in analysis. A participant was classified as being hypertensive if their average systolic blood pressure was ≥140 mmHg, and/or their average diastolic blood pressure was ≥90 mmHg [17] or if they reported being on any medication for raised blood pressure.
Waist and hip circumferences were measured to the nearest 0.5 of a centimeter using a non-stretchable standard tape measure. The waist measurement was taken mid-way between the lowest rib and the iliac crest with the subject standing at the end of gentle expiration, and hip measurement at the greater trochanters [18]. Participants were ineligible for the waist and hip measurement if pregnant, chair-bound or had a colostomy/ileostomy.
Before the waist and hip circumferences were measured, the Research Assistant requested the participant to wear light clothing. An explanation about the importance of the measurements and that clothing can substantially affect the circumference reading were provided to the participant. Thus where found necessary participants were asked to remove all outer layers of clothing, such as jackets, heavy or baggy jumpers, cardigans and waistcoats, shoes with high heels, tight garments intended to alter the shape of the body, such as corsets, lycra body suits and support tights. If the participant was wearing a belt, they were requested to remove it or loosen it for the measurements. Research Assistants received training on how to conduct these measurements during a five-day training prior to initiation of the survey.
In STEP 3, a finger-prick blood sample was collected to assess the level of plasma glucose (FPG) in the fasting state. Participants with a FPG of at least 6.1 to 6.9 mmol/L were classified as pre-diabetic while those with at least 7.0 mmol/L or on treatment for diabetes mellitus were classified as diabetic [19].
Statistical analysis
Based on an expert consultation report of 2008, the WHO provided cut-off points of waist circumference and waist-hip ratios, that suggest increased risk for metabolic complications [20, 21]. A waist circumference > 94 cm for men and > 80 cm for women indicates increased risk for metabolic complications and a waist circumference > 102 cm for men and > 88 cm for women indicates substantially increased risk for metabolic complications and a need for weight management [22]. In the analysis for this article, participants at a substantially increased risk for metabolic complications were described as abdominally obese [22, 23]. Waist circumference was preferred over waist-hip ratio as an indicator of abdominal obesity because a preliminary analysis revealed that the two measures were positively correlated. In addition, a comparative evaluation of waist-circumference, waist-hip ratio and BMI showed that waist circumference was superior to both waist-hip ratio and BMI in the prediction of single and multiple cardiovascular disease risk factors [24]. The prevalence of abdominal obesity was calculated as the percentage of participants with higher than the above stated cut-off measurements. We used the Pearson’s Chi-square statistic to assess whether there was an association between the prevalence of abdominal obesity among males and females and the various participant characteristics. The Pearson’s Chi-square statistic or the Chi-square test for independence assesses whether two categorical variables are associated/ related. In our analysis, the null hypothesis (H0) was that there was no association between the prevalence of abdominal obesity among males and females and any of the participant characteristics i.e. that the prevalence of abdominal obesity among males and females was the same across the participant sub-categories. The null hypothesis was rejected at a p-value of < 0.05.
To identify factors associated with abdominal obesity, we used weighted modified Poisson regression with robust variance [25], to estimate both the crude and adjusted prevalence rate ratios (PRR), with their corresponding 95% confidence intervals. Modified Poisson regression with robust error variance was used because there is a tendency to over-estimate the prevalence and under-estimate the standard errors of the estimated risk-ratios when the outcome is not rare as is the case with logistic regression [26]. To account for differing sampling proportions of participants per enumeration area, all analyses were done using sampling selection weights. All variables suspected to be associated with abdominal obesity were fitted into a model and removed one at time starting with the variable with the highest p-value until only those with a p-value < 0.05 were left in the model. The independent variables included in the model were age, sex, and marital status, level of education, geographical region of residence, urban or rural residence, employment status, fruit and vegetable consumption, level of physical activity, alcohol use, blood pressure and FPG. All statistical analyses were performed using STATA version 12 (StataCorp, College Station, Texas, USA).
Results
Participants and their characteristics
From the sample size calculation, 4900 participants were targeted of whom 3987 agreed to participate, yielding a participation rate of 81.4%. Of the 3987 participants, 3676 had measurements for both waist and hip circumference and are included in this analysis. Of the 3676 participants, 1562 (42.5%) were males, 2688 (73.1%) resided in rural areas and 2398 (65.3%) were either married or cohabiting (Table 1).
Table 1.
Characteristic | -n- | % |
---|---|---|
Sex | ||
Male | 1562 | 42.5 |
Female | 2114 | 57.5 |
Age group, years | ||
18–24 | 846 | 23.0 |
25–34 | 1089 | 29.6 |
35–44 | 795 | 21.6 |
45–54 | 538 | 14.6 |
55–64 | 289 | 7.9 |
≥ 65 | 119 | 3.2 |
Mean ± SD | 35.8 ± 13.1 | |
Residence | ||
Rural | 2688 | 73.1 |
Urban | 988 | 26.9 |
Region | ||
Eastern | 1178 | 32.1 |
Central | 904 | 24.6 |
Northern | 695 | 18.9 |
Western | 899 | 24.5 |
Ethnicity | ||
Baganda | 713 | 19.4 |
Banyankore/Bakiga | 667 | 18.2 |
Basoga | 291 | 7.9 |
Banyoro/Batooro | 236 | 6.4 |
Lugbara/Madi | 229 | 6.2 |
Other | 1539 | 41.9 |
Marital status | ||
Never married | 602 | 16.4 |
Married/Cohabiting | 2398 | 65.3 |
Separated/Divorced/Widowed | 673 | 18.3 |
Completed level of education | ||
No formal school | 612 | 16.7 |
Primary school | 1497 | 40.9 |
Secondary school | 1203 | 32.8 |
University or higher | 351 | 9.6 |
Employment status | ||
Not employed | 1257 | 34.2 |
Employed | 2418 | 65.8 |
Prevalence of abdominal obesity among adults in Uganda
Among the males, 20 (1.3%) were abdominally obese as were 412 (19.5%) among the females, (p < 0.05) (Table 2). Overall, 432 (11.8%) were abdominally obese. In urban areas 160 (16.2%) were abdominally obese as were 272 (10.1%) in rural areas. The prevalence of abdominal obesity among men and women was significantly associated with marital status (p = 0.01). Men had a mean waist circumference of 77.4 cm while women had a mean waist circumference of 80.7 cm, and 79.3 cm overall.
Table 2.
Variable | -n- | # of persons with abdominal obesity –n-(%) | Males n = 1562 | Females n = 2114 | p* |
---|---|---|---|---|---|
All | 3676 | 432 (11.8) | 20 (4.6) | 412 (95.4) | < 0.05 |
Age | |||||
18–24 | 846 | 41 (4.8) | 3 (7.3) | 38 (93.7) | 0.31 |
25–34 | 1089 | 99 (9.1) | 1 (1) | 98 (99) | |
35–44 | 795 | 124 (15.6) | 7 (5.6) | 117 (94.4) | |
45–54 | 538 | 91 (16.9) | 5 (5.5) | 86 (94.5) | |
55–64 | 289 | 55 (19.0) | 4 (7.3) | 51 (92.7) | |
≥ 65 | 119 | 22 (18.5) | 0 (0) | 22 (100) | |
Rural-urban residence | |||||
Urban | 988 | 160 (16.2) | 11 (6.9) | 149 (93.1) | 0.09 |
Rural | 2688 | 272 (10.1) | 9 (3.3) | 263 (96.7) | |
Marital status | |||||
Never married | 602 | 22 (3.6) | 3 (13.6) | 19 (86.4) | 0.01 |
Married/Cohabiting | 2398 | 283 (11.8) | 16 (5.7) | 267 (94.3) | |
Other | 673 | 126 (18.7) | 1 (0.8) | 125 (99.2) | |
Employment | |||||
Employed | 2418 | 304 (12.6) | 18 (5.9) | 286 (94.1) | 0.05 |
Unemployed | 1257 | 128 (10.2) | 2 (1) | 126 (99.0) | |
Fruit & Veg servings/ day | |||||
≥ 5 | 566 | 59 (10.4) | 3 (5.1) | 56 (94.9) | 0.93 |
1–4 | 2958 | 353 (11.9) | 17 (4.8) | 336 (95.2) | |
Met WHO recommendation for physical activity | |||||
Yes | 3574 | 413 (11.6) | 18 (4.4) | 395 (95.6) | 0.21 |
No | 102 | 19 (18.6) | 2 (10.5) | 17 (89.5) | |
Alcohol use in standard drinks per occasion | |||||
Never | 1905 | 253 (13.3) | 9 (3.6) | 244 (96.4) | 0.06 |
Ever or ≤ 6 | 1385 | 145 (10.5) | 6 (4.1) | 139 (95.9) | |
> 6 | 361 | 31 (8.6) | 4 (12.9) | 27 (87.1) | |
Hypertensive | |||||
No | 2705 | 241 (8.9) | 7 (2.9) | 234 (97.1) | 0.06 |
Yes | 971 | 191 (19.7) | 13 (6.8) | 178 (93.2) | |
FPG (mmol/L)c | |||||
< 6.1 | 3309 | 376 (11.4) | 13 (3.5) | 363 (96.5) | < 0.05 |
6.1–6.9 | 58 | 9 (15.5) | 3 (33.3) | 6 (66.7) | |
> 7.0 or on DM Rx | 309 | 47 (15.2) | 4 (8.5) | 43 (91.5) |
cFasting Plasma Glucose in mmol/L
p* p-value for a Chi-square test for independence comparing the prevalence of abdominal obesity among males and females across participant sub-categories
Factors associated with abdominal obesity
The factors significantly associated with abdominal obesity were sex, marital status, level of education, urban/ rural residence and blood pressure. Compared with males, female participants were more likely to be abdominally obese APRR 7.59 [5.58–10.33] (Table 3). Participants who were married or cohabiting APRR 1.82 [1.29–2.57] and participants who were separated or divorced APRR 1.69 [1.17–2.46] were more likely to be abdominally obese compared with participants who had never married before. Compared with rural dwellers, participants from urban areas were more likely to be abdominally obese APRR 1.29 [1.09–1.53]. Compared with participants with normal blood pressure, participants with elevated blood pressure or on treatment for elevated blood pressure were more likely to be abdominally obese APRR 1.83 [1.57–2.14]. Compared with participants without any education, participants with secondary education were more likely to be abdominally obese APRR 1.42 [1.12–1.78].
Table 3.
Variable | Males | Females | Males and Females | |||
---|---|---|---|---|---|---|
Crude PRRa [95% CI] | Adjusted PRR [95% CI]* | Crude PRR [95% CI] | Adjusted PRR [95% CI]** | Crude PRR [95% CI] | Adjusted PRR [95% CI]*** | |
Sex | ||||||
Males | – | – | – | – | 1.0 | 1.0 |
Females | – | – | – | – | 8.70 [6.19–12.22] | 7.59 [5.58–10.33] |
Age | ||||||
18–24 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
25–34 | 0.56 [0.21–1.49] | 0.76 [0.29–1.97] | 1.04 [0.80–1.34] | 0.97 [0.76–1.25] | 1.00 [0.78–1.28] | 0.97 [0.76–1.25] |
35–44 | 0.35 [0.13–0.99] | 1.03 [0.40–2.63] | 1.11 [0.85–1.48] | 1.08 [0.82–1.42] | 1.04 [0.80–1.35] | 1.05 [0.81–1.36] |
45–54 | 0.42 [0.12–1.43] | 0.64 [0.22–1.86] | 0.92 [0.67–1.26] | 0.90 [0.66–1.23] | 0.85 [0.62–1.16] | 0.86 [0.63–1.17] |
55–64 | 0.27 [0.07–1.08] | 0.62 [0.20–1.91] | 1.08 [0.75–1.57] | 1.02 [0.72–1.46] | 0.97 [0.68–1.39] | 0.94 [0.66–1.33] |
≥ 65 | 0.39 [0.05–2.89] | 0.58 [0.12–2.77] | 1.23 [0.79–1.91] | 1.22 [0.84–1.78] | 1.11 [0.71–1.73] | 1.11 [0.75–1.65] |
Marital status | ||||||
Never married | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
Married/Cohabiting | 2.01 [0.90–4.51] | 1.16 [0.59–2.27] | 2.03 [1.31–3.15] | 2.08 [1.39–3.13] | 1.85 [1.27–2.70] | 1.82 [1.29–2.57] |
Other | 1.56 [0.52–4.68] | 0.68 [0.26–1.82] | 1.83 [1.14–2.91] | 1.92 [1.25–2.94] | 1.67 [1.11–2.50] | 1.69 [1.17–2.46] |
Level of education | ||||||
No formal schooling | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
Primary | 0.57 [0.16–2.03] | 0.60 [0.24–1.50] | 1.18 [0.95–1.47] | 1.18 [0.95–1.46] | 1.15 [0.91–1.46] | 1.17 [0.94–1.46] |
Secondary | 1.14 [0.34–3.76 | 1.08 [0.42–2.81] | 1.44 [1.13–1.83] | 1.40 [1.12–1.75] | 1.42 [1.10–1.84] | 1.42 [1.12–1.78] |
University or higher | 0.71 [0.19–2.68] | 0.92 [0.31–2.70] | 1.18 [0.82–1.68] | 1.12 [0.78–1.60] | 1.15 [0.80–1.66] | 1.19 [0.84–1.67] |
Region of residence | ||||||
Eastern | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
Central | 0.64 [0.22–1.85] | 0.54 [0.22–1.31] | 0.99 [0.76–1.28] | 0.93 [0.72–1.20] | 0.96 [0.75–1.23] | 0.87 [0.69–1.11] |
Northern | 1.26 [0.54–2.89] | 0.85 [0.37–1.98] | 1.15 [0.92–1.44] | 1.08 [0.86–1.36] | 1.13 [0.89–1.44] | 1.03 [0.82–1.30] |
Western | 0.86 [0.35–2.11] | 0.51 [0.20–1.31] | 1.23 [0.99–1.52] | 1.18 [0.96–1.45] | 1.19 [0.96–1.48] | 1.15 [0.94–1.41] |
Rural-urban residence | ||||||
Rural | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
Urban | 1.47 [0.68–3.18] | 1.80 [0.98–3.31] | 1.33 [1.10–1.60] | 1.29 [1.09–1.54] | 1.31 [1.08–1.58] | 1.29 [1.09–1.53] |
Employment | ||||||
Unemployed | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
Employed | 0.72 [0.33–1.54] | 0.93 [0.45–1.91] | 1.25 [1.05–1.49] | 1.22 [1.04–1.43] | 1.22 [1.01–1.47] | 1.18 [0.99–1.40] |
Fruit & Veg servings/ day | ||||||
≥ 5 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
1–4 | 0.69 [0.32–1.47] | 0.85 [0.38–1.91] | 0.92 [0.75–1.13] | 0.94 [0.77–1.15] | 0.90 [0.73–1.12] | 0.93 [0.75–1.15] |
Met WHO recommendation for physical activity | ||||||
Yes | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
No | 1.76 [0.28–10.92] | 1.55 [0.37–6.42] | 1.03 [0.66–1.61] | 0.92 [0.59–1.45] | 1.05 [0.70–1.59] | 0.90 [0.59–1.35] |
Alcohol use in standard drinks per occasion | ||||||
Never | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
Ever or ≤ 6 | 1.44 [0.74–2.78] | 0.89 [0.45–1.75] | 1.00 [0.84–1.19] | 0.97 [0.82–1.16] | 1.01 [0.85–1.21] | 0.99 [0.83–1.17] |
> 6 | 1.53 [0.61–3.85] | 1.07 [0.47–2.45] | 1.15 [0.81–1.64] | 1.12 [0.79–1.59] | 1.19 [0.85–1.65] | 1.20 [0.87–1.66] |
Hypertensive | ||||||
No | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
Yes | 8.85 [4.19–18.71] | 10.15 [4.78–21.53] | 1.59 [1.33–1.99] | 1.60 [1.36–1.89] | 1.79 [1.52–2.12] | 1.83 [1.57–2.14] |
FPG (mmol/L) | ||||||
< 6.1 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 | 1.0 |
6.1–6.9 | 3.98 [1.14–13.91] | 2.52 [0.80–8.00] | 0.98 [0.55–1.78] | 0.99 [0.56–1.78] | 1.18 [0.72–1.95] | 1.22 [0.74–2.01] |
> 7.0, or on DM Rx | 2.24 [1.05–4.76] | 2.45 [1.32–4.54] | 1.14 [0.88–1.48] | 1.13 [0.88–1.45] | 1.22 [0.94–1.59] | 1.24 [0.96–1.60] |
aPrevalence Rate Ratio
*Adjusted for blood pressure and FPG
**Adjusted for marital status, level of education, urban/rural residence, employment status and blood pressure
***Adjusted for sex, marital status, level of education, urban/rural residence and blood pressure
Discussion
The survey estimated that 11.8% of adults in Uganda are abdominally obese with men and women having a mean waist circumference of 77.4 cm and 80.7 cm respectively. Sociologically, the high prevalence of abdominal obesity in Uganda has been attributed to a society in which plumpness is associated with wealth, respect, dignity, confidence and beauty [27, 28].
Compared with Uganda, the mean waist circumference reported in Botswana was higher among both men (82.5 cm) and women (88.4 cm) [29]. Similarly, the mean waist circumference reported in Tanzania was higher among both men (80.6 cm) and women (84.9 cm) [30] compared to the results of this study. In Kenya however, although the mean waist circumference was higher (78.6 cm) among men compared with Uganda, the women in Kenya had a lower mean waist circumference (79.1 cm) [31].
All the surveys consistently reported higher mean waist circumference among women compared with men. In the association analysis, sex was also found to be a significant predictor of abdominal obesity. This difference in the extent of abdominal fat deposition between women and men is no surprise finding and has been documented elsewhere [32–34]. It has been attributed to the difference in sex steroid hormones that drive the divergence in body structure and composition particularly during adolescence. In fact, even among men, the amount of free and total testosterone is inversely associated with the degree of abdominal obesity [35]. Some researchers however have further attributed this difference to the dissimilarities in the environment and genetic susceptibility of fat accumulation [36] between men and women. Biologically though, the increased waist circumference in females could also be related to increasing parity [37] as pregnancy leads to an increase in visceral and abdominal fat postpartum [20] and a post-menopausal redistribution of body fat to the abdominal area [38]. Interventions for the control and prevention of unhealthy abdominal weight gain should bear in mind the biological differences between men and women and address the socio-cultural perceptions surrounding abdominal obesity in Uganda.
We also found that participants who were married, separated or divorced were more likely to be abdominally obese. The literature on the association between marital status and abdominal obesity is inconsistent. Some researchers have reported similar positive associations between being married or formerly married and weight gain [39] while others have reported different patterns among married people, between women and men [40]. The likelihood of married people being more abdominally obese has been attributed to a change of dietary patterns after marriage and increased social support. Married people are more likely to have a more stable eating pattern and the social support that comes from the responsibility of eating together [41].
The analysis also revealed a consistent association between high blood pressure and abdominal obesity. Similar associations have been reported in cross-sectional studies [42] and longitudinal studies [43]. After following up participants for 13 years, Larsson and colleagues posited that it was because the adipocytes around the abdomen are unique in such a way that they deposit their free fatty acids directly into the portal vein which increases the amount of fatty acids in the liver. The elevated free fatty acid concentration results in an increase in the contents of the portal blood vessels leading to high blood pressure [44]. Strategies aimed at the control and prevention of abdominal obesity should entail screening to identify persons with elevated blood pressure for early detection, management and treatment.
The analysis also revealed significant associations between urban or rural residence, level of education and abdominal obesity. Urban residence has previously been associated with obesity [11] and has been attributed to the rapid globalization and trends towards unhealthy diets and sedentary lifestyles [45] in urban areas. Higher level of education might explain abdominal obesity because it is a proxy indicator of higher socio-economic status. In Uganda, overweight, raised blood pressure and raised cholesterol are common among people with higher socio-economic status [46] which can also be reflected in the level of education [47]. Higher education and wealth have also been shown to correlate with higher weight status among people in Uganda [3]. Strategies for economic development should also promote active lifestyles and healthy food choices so that the socio-economic gains are not diluted by the individual and health system costs of treating abdominal obesity related complications.
Strengths and limitations
The findings of this study are subject to a number of limitations. First, because mean waist circumference can depend on ethnic group and gender, and yet the cut-offs for abdominal obesity that were used were based on reports from European populations [20], it is likely that there was misclassification of those at risk. However the few studies that have reported the cut-offs for abdominal obesity and risk of metabolic complications in African populations have quoted more conservative cut-offs [48, 49]. This means that the misclassification led to under-estimation and not over-estimation of the prevalence consequently biasing the associations towards the null. Secondly because of the cross-sectional nature of the study design, we cannot make inferences on causality. Also, information on socio-demographic characteristics and some risk factors were assessed using self-reporting which is a source of information bias. However the main outcome measure was assessed using a standard protocol. In addition, findings from the survey are representative of the Uganda adult population and can be compared with findings from other countries that used the same protocol.
Conclusions
There is a high prevalence of abdominal obesity among adults in Uganda which puts many at risk of developing associated metabolic complications. These data provide useful information for developing interventions and formulation of policies for the control and prevention of abdominal obesity in Uganda.
Acknowledgements
The authors are grateful to the people who volunteered to participate in the survey; and for the technical and administrative support provided by Uganda’s Ministry of Health, the Uganda Bureau of Statistics. The authors also acknowledge the technical support provided by the Department of Prevention of Non-communicable Diseases, Non-communicable Diseases and Mental Health Cluster, World Health Organization, Geneva, Switzerland.
Funding
The conduct of the survey was supported by funding from the Uganda government, the World Health Organization, the World Diabetes Foundation, and the United Nations Development Program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
The data that were used in this analysis can be accessed by writing an email to the first author.
Abbreviations
- APRR
Adjusted Prevalence Rate Ratio
- BMI
Body Mass Index
- NCD
Non Communicable Diseases
- PRR
Prevalence Rate Ratio
- STEPS
Stepwise Approach to Surveillance
- UDHS
Uganda Demographic Health Survey
- WHO
World Health Organization
Authors’ contributions
GM, SKB, RW and DG designed and implemented the study. SNK and BK performed statistical analysis. SKB, RW, SNK, BK and DG were involved in the review and interpretation of results. DG, SNK and BK were responsible for the final content of the paper. All authors approved the final version of the article.
Ethics approval and consent to participate
Written informed consent was sought from each participant prior to conducting any study procedures. The study was also reviewed and approved by the Institutional Review Committee of Nsambya Hospital, Kampala, Uganda, and registered with the Uganda National Council for Science and Technology.
Consent for publication
Not applicable.
Competing interests
All authors declare that they have no competing interests.
Publisher’s Note
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Steven Ndugwa Kabwama, Email: skabwama@musph.ac.ug.
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Associated Data
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Data Availability Statement
The data that were used in this analysis can be accessed by writing an email to the first author.