Screening results
The initial electronic bibliographic database searches yielded 11 803 potentially eligible articles (Supplementary Appendix No. 1 Table 4). Following title screening, 10 918 articles were excluded, and 885 met the eligibility criteria (Figure 1) and were exported to the EndNote X9 (version 19.1.0.12691) virtual library explicitly created for this study. Hand-searching yielded 19 articles that could not be captured by the search strategy, which were also exported to EndNote X9 virtual library. A total of 105 duplicates was removed from the library, leaving 799 articles eligible for abstract screening. Following abstract screening, 93 articles were considered suitable for thorough assessment in full-article screening, during which 71 of them were excluded. Full-article screening yielded 22, which were selected for inclusion in data extraction and were included in the current systematic review. Nineteen articles were included in the meta-analysis. All articles were included in the narrative synthesis. See Figure 1 for the PRISMA flow chart detailing the study selection and exclusion process.
After the full-article screening, we measured the degree of the agreement (see Table 6 in the Supplementary Appendix No. 1). The results showed that there was a 92.5 per cent agreement versus 62.2 per cent expected by chance, which constitutes a considerably high agreement between screeners (Kappa statistic = - 0.80 and p-value <0.05). Also, the McNemar’s chi-square statistic suggests that there is no statistically significant difference in the proportions of yes/no answers by reviewers with p-value > 0.05.
Risk of bias assessment
All 22 primary studies eligible for inclusion, were subjected to a methodological quality assessment utilizing the Mixed Methods Appraisal Tool (MMAT) – Version 2018.17 The studies were evaluated using all the considered domains. Once all the studies were assessed, three were rated 100 per cent, six as 86 per cent, twelve as 71 per cent, and one as 57 per cent (see Table 5 in the Supplementary Appendix No. 1). Nine of the 22 included studies were therefore deemed high quality (75–100% score). We could not explore publication bias by examining the funnel plots for asymmetry, because, in the presence of high heterogeneity, there is no reason to expect a plot of estimates against their SEs to have a funnel shape.
Characteristics of Included Studies
In total, 22 studies were retained for analysis, 20 studies contributed data for children (00-14 years), youths (15-24 years) and adults (25-64 years), and only 2 studies contributed data for seniors (≥ 65 years). The baseline characteristics and significant findings of the included studies are presented in Table 3.
a) Study participants and geographical setting
All twenty-two included studies were cross-sectional by design, and each of the studies focused on the different geographic settings, distributed across four regions of the sub-Saharan Africa (see Figure 2). A large proportion of the studies (n = 10 studies) was conducted in urban settings,24-33 and four studies were conducted in rural settings only.34-37 One study was conducted in a peri-urban38 and one study in a semi-rural setting.39 The remaining six studies recruited participants from both rural and urban settings.40-45
Overall, the studies selected for inclusion (n = 22 studies) involved a total of 26 609 participants, 12 453 (46.8%) participants were males, and one study recruited only women of reproductive age living in informal settlements in Accra, Ghana 29. The distribution of the rest of the studies by countries was as follows: 4 from Ethiopia,25, 27, 40, 41; 1 Nigeria,24; 1 Madagascar,26; 3 Ghana,29, 38, 39; 1 Zambia,37; 2 Tanzania,28, 35; 1 Malawi,34; 1 Cameroon,33; 2 Sudan,30, 31; 1 Burkina Faso,42; 1 Kenya,32; 1 Botswana,45 and 3 studies from South Africa36, 43, 44. Figure 2 shows the study distribution from the four regions of sub-Saharan Africa, with only 1 study from Central Africa33 and 12 from Eastern Africa.
b) Food Insecurity
In assessing food insecurity exposure in the original publication, across the twenty-two included studies, this was generally measured either at a household level or at an individual level and indicated categorically. In this group of studies, a subset (n = 3 studies) involved designs where researchers measured food insecurity at the household level using the food insecurity access scale criterion.32, 37, 40 Another subset (n = 9 studies) measured food insecurity at an individual level using the Minimum Adequate Diet criterion, 24, 25, 27, 31, 33, 36, 37, 42, 43 the Minimum Dietary Diversity criterion (n = 5 studies),28, 29, 38, 39, 45 and the last subset (n = 4 studies) used more than one tool to gauge food insecurity.30, 37, 44, 45 While studies on children ≤ 5 years used the Minimum Meal Frequency criterion,30 the Weight-for-height criterion,34 and the Quetelet index26 to ascertain food insecurity. See Table 1 in the Supplementary Appendix No. 1 for a detailed list of reported tools/ methods definitions and theoretical minimum risk exposure level/ scales used to ascertain food insecurity for each study.
c) Metabolic Risk Factors
Collectively, the included studies presented prevalence data on a variety of metabolic risk factors, using a total of nine international diagnostic criteria to diagnose metabolic risk factors (see Table 2 in the Supplementary Appendix No. 1). In the current review, the WHO STEPwise approach to chronic disease risk factor surveillance diagnostic criteria was found to be the most used diagnostic tool (n = 8 studies);24, 25, 27-29, 36, 37, 42 while self-reported pretested questionnaire followed by a physical examination to confirm condition was the second most used diagnostic tool (n = 5 studies).30, 33, 38, 40, 41 One study on seniors ≥ 60 years used the WHO Global Aging and Adult Health (SAGE) criteria to diagnose for metabolic risk factors.43
Results of Individual Studies
a) Evidence on the associations between food insecurity and metabolic risk factors
In summary, all twenty-two included studies contributed strong evidence on the association between food insecurity and key metabolic risk factors on the causal pathway to diet-sensitive NCDs in children (00-14 years), youths (15-24 years), adults (25-64 years), and senior (≥ 65 years) participants pooled across sub-Saharan African countries (n = 9 studies of high quality 75-100%, n = 13 of average quality 51 – 75%) (Table 3).
Twenty of the included studies (n = 8 studies of high quality 75-100%, and n = 12 of average quality 51 – 75%) consistently suggested an adverse association between reported key metabolic risk factors and exposure to food insecurity, that is, seven studies on children (00-14 years), four studies on the youth (15-24 years), seven studies on adults (25-64 years), and two studies on the senior (≥ 65 years) participants, as shown in Table 3.
Of the two remaining studies, Gebremichael et al.41 (n = 1 of high quality, 86%) reported that the was no statistically significant association between hypertension and food insecurity exposure in adults-only study participants. In contrast, Omech et al.45 (n = 1 of average quality, 71%) in adults-only study participants, found that although consumption of vegetables, fruit, and berries showed a protective effect on dyslipidaemia and obesity, it was not statistically significant; thus the association between dyslipidemia, obesity, and exposure to food insecurity was inconclusive.
b) Prevalence of metabolic risk factors among the pooled study participants
Furthermore, all twenty-two included studies contributed prevalence estimates data on the spectrum of crucial metabolic risk factors, i.e., obesity, hypertension, underweight, dyslipidaemia and overweight patterned by food insecurity exposure, across four regions of sub-Saharan Africa, including variability in incidence by age, gender, and region. The prevalence estimates of the spectrum of metabolic risk factors pooled from the 22 included studies, varied considerably within gender and geographical regions, as Figure 3 illustrates.
The frequency table (see Table 4) shows the pooled number of participants diagnosed with the various metabolic risk factors relative to the total number diagnosed for males and females. The percentage with respects to these totals is shown in parenthesis. A total of 11 545 (43,4%) out of 26 609 food-insecure participants were diagnosed with different metabolic risk factors.
The prevalence estimates of key metabolic risk factors reported ranged from the lowest in Western Africa, Ghana (63/1165; 5.4%)39 to the highest in Southern Africa, South Africa (1172/1403; 83.5%)36 (see Table 6 in Supplementary Appendix No. 1). For hypertension (males 28.8%, females 42.5%) and obesity (males 6.2%, females 14.2%) there were 12 studies conducted in all four regions of sub-Saharan Africa with data that could be pooled.
Dyslipidaemia was reported in four studies (males 7.5%, females 3.7%) conducted in Western Africa, Southern Africa, and Eastern Africa. Status as overweight was reported in eight studies (males 7.1%, females 8.9%) conducted in all four regions of the sub-Saharan Africa, while status as underweight was reported in six studies (males 11.3%, females 3.49%) among adults’ participants in Central Africa, Western Africa, and Eastern Africa. Lastly, the prevalence for stunting (males 38%, females 25%), Acute Respiratory Infections (ARI) (males 0.86%, females 0.38%), and Left Ventricular Mass (males 0.97%, females 1.16%) was reported in four studies conducted in Eastern Africa only, among participants age ≤ six years.
There appears to be a slight difference between female participants (44.6%) who were diagnosed with the different key metabolic risk factors and their male counterparts (42.1%) who were also diagnosed. The derived prevalence estimates in males ranged from the lowest (134/501; 26.75%) in Central Africa to the highest in (3001/7006; 42.83%) Eastern Africa. Notably, the prevalence estimates of obesity, hypertension, and status as overweight were considerably more frequent in females than males. While dyslipidemia, being underweight and stunting were more prevalent in males (see Figure 3).
Results of Meta-analysis
Only 19 studies were of sufficient quality for inclusion for meta-analysis. The prevalence estimates were combined across studies using the random-effect model for meta-analysis. The results are summarised and presented in the forest plots (Figure 4 and Figure 5). Due to the low number of studies that reported stunting, acute respiratory infection, and left ventricular mass types of metabolic risk factors (less than 3), a meta-analysis could not be undertaken for those studies.
a) Meta-weighted prevalence of underweight and overweight
The pooled prevalence of being underweight, derived from six studies, was 12.2 per cent (95% CI: 7.0% to 18.5%), irrespective of diagnostic criteria (Figure 4a). Substantial heterogeneity was detected by I2 statistic (I2 = 97.14% p-value < 0.00) between each of the six studies. The pooled prevalence of being overweight, derived from seven studies, was 15.8 per cent (95% CI: 10.6% to 21.7%) and the observed heterogeneity detected at I2 = 96.89 per cent p-value < 0.00 respectively (Figure 4b).
b) Meta-weighted prevalence of hypertension, obesity, and dyslipidaemia
The pooled prevalence of hypertension and obesity, derived from 12 studies was 24.7 per cent (95% CI: 15.6% to 35.1%, I2 = 99.4% p-value < 0.00) (Figure 5c), and 12.8 per cent (95% CI: 7.4% to 19.5%, I2 = 98.85% p-value < 0.00) respectively (Figure 5d). The pooled prevalence of dyslipidaemia, derived from 3 studies was 27.6 per cent (95% CI: 6.5% to 54.9%), heterogeneity was detected by I2 statistic at I2 = 99.18% p-value < 0.00 (Figure 5e).
c) Exploration of heterogeneity
The overall pooled prevalence estimate of key metabolic risk factors was 41.8 per cent (95% CI: 33.2% to 50.8%), and a high degree of heterogeneity between the 19 studies was detected at I2 = 99.5 per cent p-value < 0.00. Sensitivity analyses, an exploration of the possible cause of significant heterogeneity, were not formally conducted, due to the low number of the group of studies reporting on these outcomes, i.e., obesity, hypertension, being underweight, dyslipidaemia and being overweight, providing scant ability to detect them. Hence, there were not enough variations observed in the following study-level characteristics: study quality score, study geographical region, and diagnostic criteria to justify different groupings.