Background: Neural tube defects (NTDs) are a group of disorders that arise from the failure of the neural tube close between 21 and 28 days after conception. About 90% of neural tube defects and 95% of death due to these defects occurs in low-income countries. Since these NTDs cause considerable morbidity and mortality, this study aimed to determine the prevalence and associated factors of NTDs in Africa. Methods: The protocol of this study was registered in the International Prospective Register of Systematic Reviews (PROSPERO number: CRD42020149356). All major databases such as PubMed/MEDLINE, EMBASE, CINAHL, Web of Science, African Journals Online (AJOL), and Google Scholar search engine were systematically searched. A random-effect model was used to estimate the pooled prevalence of NTDs in Africa, and Cochran’s Q-statistics and I2 tests were used to assess heterogeneity between included studies. Publication bias was assessed using Begg ’s tests, and the association between determinant factors and NTDs was estimated using a random-effect model. Results: Of the total 2679 articles, 37 articles fulfilled the inclusion criteria and were included in this systematic review and meta-analysis. The pooled prevalence of NTDs in Africa was 50.71 per 10,000 births (95% CI: 48.03, 53.44). Folic acid supplementation (AOR: 0.40; 95% CI: 0.19–0.85), maternal exposure to pesticide (AOR: 3.29; 95% CI: 1.04–10.39), mothers with a previous history of stillbirth (AOR: 3.35, 95% CI: 1.99–5.65) and maternal exposure to x-ray radiation (AOR 2.34; 95% CI: 1.27–4.31) were found to be determinants of NTDs. Conclusions: The pooled prevalence of NTDs in Africa was found to be high. Maternal exposure to pesticides and x-ray radiation were significantly associated with NTDs. Folic acid supplementation before and within the first month of pregnancy was found to be a protective factor for NTDs.
The protocol of this study was registered in the International Prospective Register of Systematic Reviews (PROSPERO), the University of York Centre for Reviews and Dissemination (ID number: CRD42020149356) [14]. This review and meta-analysis were conducted according to the guideline of Preferred Reporting Items for Systematic reviews and Meta-Analysis (PRISMA) (additional file 1) [15]. A systematic review and meta-analysis were conducted using published and unpublished articles on the prevalence and associated factors of NTDs in Africa. The databases used to search for studies were PubMed, EMBASE, Google Scholar, CINAHL, POPLINE, and African Journals Online (AJOL), and grey literature was searched on Google and Research Gate. The following vital terms neural AND tube AND defect AND “determinant factors” OR “associated factors” OR “protective factors” OR “risk factors” AND “Africa countries” were used separately or in combination with the Boolean operator’s terms “AND” and “OR.” The search was also done by combining the above search terms with the names of all countries included in Africa and the sub-region of Africa (additional file 2). The reference lists of the retrieved studies were also scanned to access additional articles and screened against our eligibility criteria. Any study in Africa that reported magnitude and determinant factors for NTDs and fulfilled the following criteria were recruited into the analysis: All studies conducted in African countries. Epidemiological studies had reported prevalence and risk factors of NTDs as an outcome. All observational studies (cross-sectional, case-control, and cohort) reporting the prevalence and determinants of NTDs were eligible for this systematic review and meta-analysis. Articles published in English were considered. Both published and unpublished articles were considered. No restriction of the period applied to this review. Important articles identified from the databases mentioned above and websites were imported into an Endnote X8, and duplicates were removed. Screening retrieved articles titles, abstracts, and full-text quality was conducted independently by two review authors (DA & KS) based on the eligibility criteria. The disagreement between the two reviewers was resolved by reaching a consensus through discussion. The study risk of bias was assessed using the Joana bridge institute (JBI) critical appraisal tool [16]. Two authors (DA & KS) evaluated the quality of the full text considered to be included in the meta-analysis. The tool consists of ten items for case-control and eight for cross-sectional studies (additional files 3 and 4). Each item for each study was judged as Yes (1) and No (0). When the information provided was not adequate to make a judgment for a specific item, we agreed to grade that item with a ‘No’ (0). Each study was graded depending on the number of items judged ‘Yes’ (1) as low risk (≥ 7), medium risk (5 to 6) or high risk (≤ 4) for cross-sectional studies and low risk (≥8), medium risk (7 to 6) and high risk (< 5) for case-control studies (additional files 3 and 4). The selected papers were thoroughly reviewed, and the required information for the systematic review was extracted and summarized using an extraction table in Microsoft Office Excel software (additional files 5 and 6). The data extraction tool consists of the name of the author (s), country and sub-region, study design, setting, year of publication, sample size, and number of NTDs (additional file 5). Data were extracted in two-by-two tables for determinants of NTDs, pooled odds ratio with their corresponding 95% confidence interval (CI) was calculated based on the original studies report (additional file 6). The extracted data were imported into STATA/SE version 14 software for all statistical analysis. The heterogeneity among all included studies was assessed by using the I2 statistics and Cochran Q test. In this meta-analysis, the tests indicate significant heterogeneity among included studies (I2 = 100, P-value <.001). For this reason, we used a random-effects model as a method of analysis. The publication bias was assessed using begg ‘s test statistics. Pooled prevalence and odds ratios along their corresponding 95% CI were presented using a forest plot. Subgroup analyses for the prevalence of NTDs were performed by sub-regions of Africa. To determine factors associated with NTDs, data were entered into Review Manager Version 5, and pooled odds ratios (ORs) with 95% confidence interval (CI) were used. Neural tube defects all newborns having one of the following defects are considered as having NTD. Spina bifida (meningocele and myelomeningocele), anencephaly, and encephalocele. Prevalence of NTDs = number of a newborn with NTDs/total number of newborns *100