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. 2016 Apr 11;11(4):e0151586. doi: 10.1371/journal.pone.0151586

Describing the Prevalence of Neural Tube Defects Worldwide: A Systematic Literature Review

Ibrahim Zaganjor 1,‡,*, Ahlia Sekkarie 1,, Becky L Tsang 1, Jennifer Williams 1, Hilda Razzaghi 1,2, Joseph Mulinare 1,2, Joseph E Sniezek 1, Michael J Cannon 1, Jorge Rosenthal 1
Editor: Rogelio Cruz-Martinez3
PMCID: PMC4827875  PMID: 27064786

Abstract

Background

Folate-sensitive neural tube defects (NTDs) are an important, preventable cause of morbidity and mortality worldwide. There is a need to describe the current global burden of NTDs and identify gaps in available NTD data.

Methods and Findings

We conducted a systematic review and searched multiple databases for NTD prevalence estimates and abstracted data from peer-reviewed literature, birth defects surveillance registries, and reports published between January 1990 and July 2014 that had greater than 5,000 births and were not solely based on mortality data. We classified countries according to World Health Organization (WHO) regions and World Bank income classifications. The initial search yielded 11,614 results; after systematic review we identified 160 full text manuscripts and reports that met the inclusion criteria. Data came from 75 countries. Coverage by WHO region varied in completeness (i.e., % of countries reporting) as follows: African (17%), Eastern Mediterranean (57%), European (49%), Americas (43%), South-East Asian (36%), and Western Pacific (33%). The reported NTD prevalence ranges and medians for each region were: African (5.2–75.4; 11.7 per 10,000 births), Eastern Mediterranean (2.1–124.1; 21.9 per 10,000 births), European (1.3–35.9; 9.0 per 10,000 births), Americas (3.3–27.9; 11.5 per 10,000 births), South-East Asian (1.9–66.2; 15.8 per 10,000 births), and Western Pacific (0.3–199.4; 6.9 per 10,000 births). The presence of a registry or surveillance system for NTDs increased with country income level: low income (0%), lower-middle income (25%), upper-middle income (70%), and high income (91%).

Conclusions

Many WHO member states (120/194) did not have any data on NTD prevalence. Where data are collected, prevalence estimates vary widely. These findings highlight the need for greater NTD surveillance efforts, especially in lower-income countries. NTDs are an important public health problem that can be prevented with folic acid supplementation and fortification of staple foods.

Introduction

Neural tube defects (NTDs), serious birth defects of the brain and spine, are a major, preventable public health burden. Globally, it is estimated that approximately 300,000 babies are born each year with NTDs [1], resulting in approximately 88,000 deaths and 8.6 million disability-adjusted life years (DALYs) [2, 3]. In low income countries, NTDs may account for 29% of neonatal deaths due to observable birth defects [4]. As morbidity and mortality from infectious diseases are decreasing worldwide, the contribution of birth defects to under-5 morbidity and mortality will continue to increase proportionally [5].

Conclusive evidence from clinical trials has led to recommendations for adequate periconceptional folic acid intake to reduce the occurrence of a NTD-affected pregnancy [6]; as a result, mandatory folic acid fortification (FAF) of staple cereal grains has been legislated in many countries as recently reviewed [7, 8]. Long-term surveillance of NTDs in countries that have successfully implemented fortification, such as the United States, Canada, Costa Rica, South Africa, and Chile, and data from a supplementation program in China suggest that folic acid interventions can reduce NTD prevalence to as low as 5–6 per 10,000 pregnancies [8, 9].

Because birth defects are a major cause of under-5 mortality, adequate surveillance data are needed for prevention and evaluation purposes. This is particularly important for birth defects that have well-established interventions. For example, depending on the baseline prevalence, it is estimated that the majority of NTDs can be prevented with folic acid [4, 10]. However, national surveillance of NTDs and other birth defects remains limited worldwide. To promote global birth defects surveillance efforts, in 2010 the World Health Assembly issued a resolution urging member states “to develop and strengthen registration and surveillance systems for birth defects” [11].

There have been recent efforts to model and estimate the worldwide burden of NTDs and other major birth defects [1, 12]. Some data are also available from systematic reviews, but most of the reviews are specific to certain regions or income levels [1315]. However, an accurate estimate of the prevalence of NTDs in most countries is still unknown primarily due to insufficient and fragmented data collection. To complement previous efforts, the goal of our review is to describe the most current prevalence estimates of NTDs worldwide, while highlighting key methodological differences and gaps in available data.

Methods

Search Strategy

We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (S1 Document) [16]. We searched the following bibliographic databases for English and Spanish language literature published between January 1990 and July 2014: the Cochrane Collaboration, CINAHL, Embase, POPLINE, PubMed, Global Health (CDC resource), Web of Science, and several World Health Organization (WHO) library resources (African Index Medicus, Index Medicus for the Eastern Mediterranean Region, Spanish Health Sciences Bibliographic Index, Index Medicus for the South-East Asian Region, Latin American and Caribbean Health Sciences Literature, and the World Health Organization Library Information System). We adapted the search terms to each database and included keywords for neural tube defects, congenital anomalies, epidemiology, registries, and hospitals. We also identified international birth defect registries and searched the databases/reports of the European Surveillance of Congenital Anomalies (EUROCAT), the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR), and other reports. Finally, we included additional studies and reports from hand searching reference lists of systematic reviews.

Inclusion/Exclusion Criteria and Algorithm Review

We included case-control and cross-sectional studies and reports with either a reported prevalence of NTDs (defined as anencephaly/spina bifida/encephalocele), or numerator (number of reported NTD cases) and denominator data (number of births in the study population). Many studies reported on NTDs without explaining how they defined them; we included these studies in order to increase coverage.

We excluded the following: 1) case reports and supplementation trials; 2) studies that only included anencephaly and/or encephalocele; 3) studies that only counted non-NTDs per our definition, such as amniotic band sequence, chromosomal abnormalities, or spina bifida occulta; 4) studies with a denominator of fewer than 5,000 total births given the high degree of uncertainty of NTD prevalence in such a small sample size; 5) studies that reported prevalence in graphs without point estimates; 6) studies that only used mortality data; 7) studies with data based only on prenatal diagnosis; 8) and studies whose data were collected prior to 1990. We also excluded studies that reported data after a contamination event that may have caused an increase in NTD prevalence estimates.

We developed an algorithm to ensure that the most current and relevant data for each country were included in our review. If multiple studies were available for the same region or country but at different time periods, we included the study with the most recent data. In instances where multiple studies existed for one country from different geographic locations, all studies from that country were included, except if nationally representative data were available. In these cases, only the nationally representative study was used. However, if one study reported nationwide data that were not nationally representative, we still included studies from individual regions.

Data Abstraction and Risk-of-Bias (RoB) Assessment

We abstracted data on the number of cases (numerator), the birth cohort (denominator), and calculated prevalence into a standard table. Three authors reviewed the abstracted data from the original reports and corrected errors in both abstraction and the original reports. To verify the reported prevalence estimates and to exclude syndromes, chromosomal abnormalities, isolated hydrocephalus, and spina bifida occulta cases, we re-calculated the prevalence of anencephaly, spina bifida, and encephalocele. We also calculated a sum of reported NTDs, which included spina bifida and/or anencephaly and encephalocele, depending on what NTDs the authors of the original study assessed. In addition to prevalence, we also abstracted the following information for each study: years included, geographic location, inclusion/exclusion criteria, study design (population-based vs. hospital-based), and whether the data were gathered from a birth defects registry/surveillance system. We did not distinguish between registries and surveillance systems in this review.

We developed and pre-piloted a risk-of-bias (RoB) tool to assess the quality of each study’s methodology. A study’s RoB score was based on the following components: study design, case ascertainment methods, case definition, representativeness, and limitations. The lower the RoB score, the less the study was considered to be prone to bias. Two authors reviewed each study independently and their scores were averaged for a single RoB score (possible score range: 0.0–18.0). We placed final RoB scores into quartiles: low (0.0–5.4), moderately low (5.5–7.9), moderately high (8.0–10.9), or high (11.0–18.0). We assigned the lowest RoB scores to studies that: were based on surveillance systems or registries; were population-based; were representative (as defined by the original authors to accurately describe their population of interest); included an NTD case definition; defined inclusion and exclusion criteria (e.g., gestational age, birth weight, birth outcome); and had case reporting from multiple sources.

Analysis

As part of our analyses, we stratified countries by WHO regions, World Bank income levels (low, lower-middle, upper-middle, high), presence of a surveillance system/registry, and RoB quartiles [17, 18]. For publications that did not provide NTD prevalence, we calculated the sum of reported NTDs and individual NTD type-specific prevalence estimates. In addition, if it was not provided by the reference, we calculated the 95% confidence interval for each prevalence using the Poisson distribution if the number of cases was below 30, and using the binomial distribution if the number of cases was greater than or equal to 30. We calculated the range and median reported NTD prevalence for each WHO region.

We used ArcGIS 10.2.1 (ESRI, Redlands, California) to create maps illustrating NTD prevalence distributions and registry/surveillance coverage. On the maps, NTD prevalence was classified into quintiles based on all reported prevalence estimates. If there were national data, the entire country was filled-in. In Europe, if regional data were available, this geographical level was also filled-in. In instances where multiple prevalence estimates were available at the national level, the prevalence reported by the study/report with the least RoB was selected. Graphical representations of data were created using SigmaPlot 12.5 (Systat Software, San Jose, California).

Results

PRISMA

The literature search yielded 11,614 results, of which 3,948 were duplicates. Two authors reviewed and screened the 7,666 unique titles and abstracts for inclusion and exclusion criteria. After this initial screening, we excluded 6,549 abstracts and conducted the first wave of full-text review for the remaining 1,117 citations, in which 600 more were excluded. We then evaluated the remaining 517 citations and an additional 66 hand-searched sources from reports such as ICBDSR and author contacts to ensure the most relevant sources (i.e., most up-to-date data) were included. We identified 160 unique studies and reports published between January 1990 and July 2014 that met our inclusion criteria in the final stage of review (Fig 1).

Fig 1. PRISMA Flowchart.

Fig 1

The results represent data from 75 countries. Among the 194 WHO member states, the percent reporting within each region is as follows: African (8/47; 17%), Eastern Mediterranean (12/21; 57%), European (26/53; 49%), Americas (15/35; 43%), South-East Asian (4/11; 36%) and Western Pacific (9/27; 33%). Of the countries in our review, 46% have high, 31% have upper-middle, 16% have lower-middle, and 7% have low income status as defined by the World Bank.

Of the 160 studies, 2% reported spina bifida alone, 10% spina bifida and anencephaly, 1% spina bifida and encephalocele, and 81% reported all 3 conditions (either stratified or not). Six percent of studies did not provide a clear definition of how they defined NTDs.

Prevalence of Neural Tube Defects

This systematic review demonstrates great variability in reported NTD prevalence estimates globally (range: 0.3–199.4 per 10,000 births) (Table 1) [19124]. Of note, both the lowest and highest point estimates in this global range came from studies conducted in different regions of China; Beijing [113] and Luliang [112], respectively. However, even after excluding these estimates, the global range is still quite variable (range: 1.2–124.1 per 10,000 births) (Table 1) [122, 48]. Fig 2 also illustrates that NTD prevalence estimates throughout the world are high, with approximately 80% of reported prevalence estimates above 6.0 per 10,000 births (i.e., the approximate rate that should be attainable through adequate periconceptional folic acid intake) [8].

Table 1. Neural Tube Defect (NTD) Prevalence Estimates by World Health Organization (WHO) Region*.

Country World Bank Classification Location Author Year(s) Included Prevalence Rate per 10,000 Births
Anencephaly Spina bifida Encephalocele Sum of Reported NTDs¥
Prevalence 95% CI Prevalence 95% CI Prevalence 95% CI Prevalence 95% CI
AFRICA
Algeria Upper-middle Setif Houcher, et al.[19] 2004–2006 32.2 (25.6, 38.8) 42.8[f] (35.2, 50.4) 0.3 (0.0, 2.0) 75.4 (65.4, 85.4)
Cameroon Lower-middle Yaounde Njamnshi AK, et al.[20] January 1997- December 2006 18.6 (14.9, 22.3)
Democratic Republic of Congo Low Nyankunde, Oriental Province Ahuka OL, et al.[21] January 1993–August 2001 1.1 (0.0, 6.3) 6.8 (2.5, 14.8) 2.3 (0.3, 8.2) 10.2 (4.7, 19.4)
Ghana Lower-middle Accra Anyebuno M, et al.[22] January 1991–December 1992 8.4 (4.8, 13.6) 3.1 (1.2, 6.8) 11.5 (7.2, 17.4)
Malawi Low Blantyre Msamati BC, et al.[23] 1998–1999 6.3 (3.6, 10.2) 6.3 (3.6, 10.2)
Nigeria Lower-middle Cross River and Akwa Ibom States Ekanem TB, et al.[24] 1980–2003 1.6 (1.0, 2.4) 3.7 (2.7, 4.8) 5.2 (4.0, 6.5)
Nigeria Lower-middle Jos Airede KI [25] June 1987–June 1990 3.3 (0.4, 12.1) 41.8 (27.1, 61.7) 13.4 (5.8, 26.4) 58.6[a] (39.3, 78.0)
South Africa Upper-middle Eastern Cape, Kwazulu Natal, Mpumalanga, and Free State Provinces Sayed AR, et al.[26] October 2004–June 2005 3.7 (2.2, 5.9) 5.4 (3.5, 8.0) 9.8 (6.9, 12.7)
South Africa Upper-middle Sovenga, Northern Transvaal Venter PA, et al.[27] June 1989–December 1992 17.1 (9.1, 29.2) 15.8 (8.1, 27.5) 2.6 (0.3, 9.5) 35.4 (23.4, 51.6)
South Africa Upper-middle Cape Town Viljoen DL, et al. [28] 1973–1992 11.7 (10.8, 12.6)
Tanzania Low Dar es Salaam Kinasha AD and Manji K [29] 2000–2002 1.2 (0.3, 3.0) 26.1 (20.7, 31.5) 2.9 (1.4, 5.4) 30.2 (24.4, 36.0)
EASTERN MEDITERRANEAN
Egypt Lower-middle Upper Egypt Mohammed YA, et al.[30] March 2007–October 2007 2.0 (0.1, 11.1) 10.0 (3.3, 23.3) 4.0 (0.5, 14.5) 16.0[b] (6.9, 31.5)
Iran Upper-middle Yasuj, South West Iran Ebrahimi S, et al.[31] March 2008–February 2011 38.1 (24.9, 51.3)
Iran Upper-middle Ahvaz Behrooz AG and Gorjizadeh MH [32] March 2002–March 2004 24.9 (16.4, 33.4) 15.1 (9.2, 23.3) 2.3 (0.5, 6.6) 42.2 (31.2, 53.3)
Iran Upper-middle Gorgan, Golestan Abdollahi Z, et al.[33] December 2007–December 2008 21.9 N/A
Iran Upper-middle Tehran Delshad S, et al.[34] March 2005-March 2007 8.5 (6.2, 10.8) 1.6 (0.8, 3.0) 10.1 (7.6, 12.7)
Iran Upper-middle Birjand Afshar M, et al.[35] April 1997–December 2001 15.5 (10.1, 22.7) 8.9 (5.0, 14.7) 1.8 (0.4, 5.2) 29.8 (21.6, 38.0)
Iran Upper-middle Urmia Rad IA, et al.[36] January 2001–June 2005 55.2 (43.0, 67.5) 24.8 (16.6, 33.0) 2.8 (0.8, 7.3) 82.9 (67.9, 97.8)
Iran Upper-middle Hamadan Province Farhud DD, et al.[37] 1991–1997 15.6 (8.1, 25.9) 7.0 (2.6, 15.2) 50.1 (35.2, 65.0)
Iran Upper-middle Tabriz ICBDSR 2011 Report [38] 2009 4.7 (2.4, 8.5) 0.9 (0.1, 3.1) 0.9 (0.1, 3.1) 6.5 (3.6, 10.7)
Iraq Upper-middle Al-Ramadi, Al-Anbar Governate Al-Ani ZR, et al.[39] October 2010 –October 2011 3.5 (0.4, 12.6) 15.7 (7.2, 29.8) 8.7 (2.8, 20.3) 27.9[a] (15.9, 45.2)
Iraq Upper-middle Basrah Al-Sadoon I, et al.[40] 1990 2.5 (0.5, 7.2) 7.4 (3.4, 14.1) 9.9 (5.1, 17.2)
Jordan Upper-middle North Jordan Amarin ZO and Obeidat AZ [41] 2005–2006 9.5 (5.5, 15.5)
Jordan Upper-middle Amman Aqrabawi HE [42] April 2002 –April 2003 0.0 (0.0, 7.3) 59.0 (37.9, 80.0) 3.9 (0.5, 14.2) 62.9[a] (41.2, 84.6)
Jordan Upper-middle Amman Masri AT [43] 1993–2002 3.5[c] (1.7, 6.5) 7.1[c] (4.3, 10.9) 0.4[c] (0.0, 2.0) 11.0[c] (7.1, 14.8)
Jordan Upper-middle Irbid Province Daoud AS, et al.[44] January 1991–December 1993 3.7 (2.4, 5.0) 10.0 (7.9, 12.1) 2.6 (1.7, 4.0) 16.4 (13.7, 19.1)
Kuwait Upper-middle Al-Jahara Region Madi SA, et al.[45] January 2000–December 2001 3.9 (0.8, 11.3) 2.6 (0.3, 9.3) 6.5 (2.1, 15.1)
Libya Upper-middle Benghazi Singh R and Al-Sudani O [46] 1995 7.4 (3.8, 13.0) 0.6 (0.0, 3.4) 8.0 (4.3, 13.7)
Oman High National Alasfoor D and ElSayed MK [47] 2010 6.8 N/A 23.2 N/A
Pakistan Lower-middle Swat Khattak ST, et al.[48] Januray 2007–December 2007 113.3 (85.5, 141.1) 7.2 (2.0, 18.4) 124.1[d] (95.0, 153.2)
Pakistan Lower-middle Peshawar Qazi G [49] Januray 2009–December 2009 47.2 (30.3, 70.2) 21.6 (10.8, 38.7) 68.8 (46.1, 91.6)
Pakistan Lower-middle Karachi Perveen F and Tyyab S [50] January 2000–October 2005 29.4 (17.2, 47.1) 15.6 (7.1, 29.6) 5.2 (1.1, 15.2) 50.2 (33.6, 72.1)
Pakistan Lower-middle Lahore Najmi RS [51] November 1994–October 1996; August 1997–March 1998 29.6 (19.5, 39.7) 17.0 (10.3, 26.6) 2.7 (0.6, 7.9) 49.3 (36.3, 62.3)
Pakistan Lower-middle Karachi Jooma R [52] 2002 19.8 (11.6, 30.0) 15.7 (8.5, 25.0) 3.1 (0.6, 8.9) 38.6 (26.4, 50.9)
Qatar High Doha Bener A, et al.[53] January 1985–December 2009 3.6 (2.9, 4.3) 7.3 (6.4, 8.4) 10.9 (9.7, 12.2)
Saudi Arabia High Al-Khobar Al-Jama F, et al.[54] January 1992–December 1997 22.4 (14.8, 30.0) 25.7 (17.5, 33.9) 5.4 (2.3, 10.7) 53.5 (41.7, 65.3)
Saudi Arabia High Asir Region Asindi A and Al-Shehri A.[55] January 1995–December 1998 0.4 (0.1, 1.1) 5.6 (4.0, 7.2) 1.6[a] (0.8, 2.7) 7.5[a] (5.6, 9.4)
Saudi Arabia High Jeddah Safdar OY, et al.[56] 2001–2005 7.6 N/A
Saudi Arabia High Al-Madinah Al-Munawarah Murshid WR [57] April 1996–March 1997 10.9 (6.5, 17.2) 10.9 (6.5, 17.2)
Saudi Arabia High Riyadh Hakami WS and Majeed-Saidan MA [58] January 2001–December 2010 4.5 (3.2, 5.9)
Sudan Lower-middle Omdurman Elsheikh GEA and Ibrahim SA [59] February 2003–January 2004 12.5 (7.4, 17.6) 16.3 (10.5, 22.1) 4.9 (2.2, 9.3) 33.7[a] (25.3, 42.1)
United Arab Emirates High National Al Hosani H, et al.[60] January 1999–December 2001 2.1[f] (1.4, 2.8)
EUROPE
Austria High Styria EUROCAT [61] 2003–2009 1.7 (0.9, 2.9) 4.6 (3.1, 6.4) 1.5 (0.8, 2.7) 7.7 (5.8, 10.0)
Belgium High Antwerp EUROCAT [61] 2003–2012 2.6 (2.0, 3.5) 4.5 (3.6, 5.5) 0.8 (0.5, 1.4) 8.0 (6.8, 9.3)
Belgium High Hainaut EUROCAT [61] 2003–2012 3.2 (2.3, 4.4) 4.1 (3.1, 5.4) 1.2 (0.7, 2.0) 8.5 (7.0, 10.3)
Bulgaria Upper-middle Plevin Region Kovacheva K, et al.[62] 1988–2006 20.2 (16.2, 24.2)
Croatia High Zagreb EUROCAT [61] 2003–2012 2.0 (1.1, 3.3) 1.4 (0.7, 2.6) 1.1 (0.5, 2.2) 4.5 (3.1, 6.4)
Czech Republic High National EUROCAT [61] 2003–2010 2.4 (2.1, 2.8) 3.9 (3.5, 4.3) 1.3 (1.0, 1.5) 7.6 (7.0, 8.2)
Denmark High National Pasternak B, et al.[63] 1997–2011 5.5 (4.1, 6.8)
Denmark High Odense EUROCAT [61] 2003–2012 4.1 (2.5, 6.2) 5.8 (3.9, 8.3) 1.5 (0.7, 3.1) 11.4 (8.7, 14.7)
Finland High National EUROCAT [61] 2003–2011 3.2 (2.7, 3.7) 4.0 (3.5, 4.6) 1.9 (1.5, 2.3) 9.0 (8.3, 9.9)
France High Bas-Rhin Stoll C, et al.[64] 1979–2008 4.3[a] (3.7, 4.9) 4.8[a] (4.1, 5.5) 1.2[a] (0.9, 1.5) 10.3[a] (9.3, 11.3)
France High Auvergne EUROCAT [61] 2002 2.2 (0.4, 6.6) 3.0 (0.8, 7.7) 3.0 (0.8, 7.7) 8.2 (4.1, 14.7)
France High French West Indies EUROCAT [61] 2009–2012 3.3 (1.8, 5.6) 4.0 (2.3, 6.5) 1.2 (0.4, 2.8) 8.5 (6.0, 11.8)
France High Ile de la Reunion EUROCAT [61] 2003–2012 7.3 (6.0, 8.8) 9.1 (7.6, 10.8) 2.0 (1.3, 2.9) 18.4 (16.3, 20.7)
France High Paris EUROCAT [61] 2003–2012 4.7 (3.9, 5.6) 5.1 (4.3, 6.1) 1.8 (1.3, 2.4) 11.6 (10.3, 13.0)
Germany High Northern Rhine Region Klusmann A, et al.[65] January 1996 -December 2003 1.9 (1.6, 2.2) 4.4 (3.9, 4.9) 0.8 (0.6, 1.0) 7.1 (6.5, 7.7)
Germany High Mainz EUROCAT [61] 2003–2011 3.8 (1.9, 6.9) 6.6 (4.0, 10.4) 3.5 (1.7, 6.4) 14.0 (10.0, 19.0)
Germany High Saxony-Anhalt EUROCAT [61] 2003–2012 2.0 (1.4, 2.8) 5.6 (4.6, 6.9) 1.4 (0.9, 2.1) 9.0 (7.6, 10.5)
Hungary Upper-middle National ICBDSR 2011 Report [38] 2005–2009 2.0 (1.6, 2.4) 4.4 (3.8, 5.0) 0.6 (0.4, 0.9) 7.0 (6.3, 7.7)
Ireland High National McDonnell R, et al.[66] 2009–2011 4.7 (3.8, 5.6) 5.1 (4.2, 6.0) 0.7 (0.4, 1.1) 10.4 (9.1, 11.8)
Ireland High Cork & Kerry EUROCAT [61] 2003–2012 4.9 (3.6, 6.5) 5.4 (4.0, 7.0) 1.0 (0.5, 1.9) 11.3 (9.2, 13.6)
Ireland High Dublin EUROCAT [61] 2003–2012 2.2 (1.7, 2.9) 3.0 (2.4, 3.8) 0.7 (0.4, 1.1) 5.9 (5.0, 7.0)
Ireland High South East Ireland EUROCAT [61] 2003–2012 3.3 (2.1, 4.9) 5.0 (3.6, 6.9) 0.3 (0.0, 1.0) 8.6 (6.6, 11.0)
Israel High National Zlotogora J, et al.[67] 2002–2004
Jews 4.9 N/A 2.7 N/A 8.1 N/A
Arabs and Druze 8.2 N/A 6.2 N/A 16.7 N/A
Israel High Multi-Regional ICBDSR 2011 Report [38] 2005–2009 1.3 (0.8, 1.8) 2.9 (2.2, 3.6) 0.5 (0.2, 0.9) 4.6 (3.7, 5.5)
Italy High Emilia Romagna EUROCAT [61] 2003–2012 2.2 (1.7, 2.7) 2.7 (2.2, 3.3) 0.7 (0.5, 1.0) 5.6 (4.9, 6.4)
Italy High Sicily EUROCAT [61] 2003–2004 0.5 (0.1, 1.8) 1.5 (0.5, 3.3) 0.0 (0.0, 0.9) 2.0 (0.9, 3.9)
Italy High Tuscany EUROCAT [61] 2003–2012 1.9 (1.5, 2.5) 3.1 (2.5, 3.8) 0.7 (0.4, 1.1) 5.7 (4.9, 6.6)
Italy High Campania ICBDSR 2011 Report [38] 2005–2009 3.6 (2.9, 4.2) 3.1 (2.5, 3.8) 1.0 (0.6, 1.3) 7.7 (6.7, 8.7)
Italy High Lombardy ICBDSR 2011 Report [38] 2009 2.0 (0.2, 7.1) 2.0 (0.2, 7.1) 1.0 (0.0, 5.5) 4.9 (1.6, 11.5)
Italy High North East Italy ICBDSR 2011 Report [38] 2005–2009 1.5 (1.0, 2.0) 2.5 (1.9, 3.1) 0.5 (0.2, 0.8) 4.5 (3.7, 5.3)
Malta High National EUROCAT [61] 2003–2011 2.2 (0.9, 4.3) 6.3 (4.0, 9.5) 1.6 (0.6, 3.6) 10.2 (7.2, 14.0)
Netherlands High Northern Netherlands EUROCAT [61] 2003–2012 2.6 (1.9, 3.5) 4.6 (3.7, 5.7) 0.6 (0.3, 1.0) 7.7 (6.5, 9.1)
Norway High National EUROCAT [61] 2003–2012 3.5 (3.0, 4.0) 4.7 (4.1, 5.2) 0.9 (0.7, 1.2) 9.1 (8.4, 9.9)
Poland High National EUROCAT [61] 2003–2010 0.8 (0.7, 0.9) 4.5 (4.3, 4.8) 0.6 (0.5, 0.7) 5.9 (5.7, 6.2)
Poland High Wielkopolska EUROCAT [61] 2003–2010 1.2 (0.8, 1.7) 6.3 (5.5, 7.3) 1.0 (0.7, 1.4) 8.5 (7.5, 9.6)
Portugal High South Portugal EUROCAT [61] 2003–2011 1.2 (0.8, 1.9) 1.8 (1.2, 2.5) 0.2 (0.1, 0.6) 3.2 (2.4, 4.2)
Russia High Arkhangelskaja Oblast Petrova JG and Vaktskjold A [68] 1995–2004 10.7 (9.0, 12.4) 10.4 (8.7, 12.1) 21.1 (18.7, 23.5)
Russia High Moscow ICBDSR 2011 Report [38] 2005–2009 2.9 (2.3, 3.5) 3.7 (3.0, 4.4) 1.1 (0.7, 1.4) 7.6 (6.6, 8.6)
Slovak Republic High Multi-Regional ICBDSR 2011 Report [38] 2005–2009 0.9 (0.6, 1.3) 2.2 (1.7, 2.8) 0.7 (0.4, 1.0) 3.8 (3.1, 4.5)
Spain High Barcelona EUROCAT [61] 2003–2007 4.9 (3.4, 6.8) 3.3 (2.1, 4.9) 0.8 (0.3, 1.8) 9.0 (7.0, 11.4)
Spain High Basque Country EUROCAT [61] 2003–2011 5.2 (4.2, 6.3) 4.1 (3.2, 5.2) 0.7 (0.4, 1.2) 10.0 (8.6, 11.5)
Spain High National EUROCAT [61] 2003–2012 0.3 (0.2, 0.5) 0.9 (0.6, 1.1) 0.2 (0.1, 0.3) 1.3 (1.0, 1.6)
Spain High Valencia Region EUROCAT [61] 2007–2011 2.4 (1.9, 3.1) 2.4 (1.9, 3.1) 1.5 (1.1, 2.1) 6.4 (5.5, 7.4)
Sweden High National EUROCAT [61] 2007–2011 2.8 (2.4, 3.3) 3.8 (3.3, 4.3) 1.0 (0.7, 1.3) 7.5 (6.8, 8.3)
Switzerland High National Poretti A, et al.[69] January 2001–December 2007 1.8[a, b] (1.0, 2.6) 7.8[a] (6.1, 9.5) 1.1[a] (0.6, 2.0) 10.7[a] (8.7, 12.6)
Switzerland High Vaud EUROCAT [61] 2003–2012 3.5 (2.3, 5.2) 4.5 (3.1, 6.2) 2.4 (1.4, 3.7) 10.4 (8.2, 12.9)
Turkey Upper-middle Afyonkarahisar Onrat ST, et al.[70] July 2003–December 2004 13.9 (7.2, 24.3) 19.7 (11.5, 31.5) 2.3 (0.3, 8.4) 35.9 (23.3, 48.5)
Turkey Upper-middle Izmir Mandiracioglu A, et al.[71] January 2000–December 2000 14.3[a, b] (10.4, 18.2)
Turkey Upper-middle Multi-Regional Tuncbilek E, et al.[72] July 1993–June 1994 11.0 (7.0, 16.3) 13.2 (8.4, 18.0) 5.9 (3.2, 10.2) 30.1 (22.9, 37.4)
Turkey Upper-middle Ankara Himmetoglu O, et al.[73] 1988–1995 34.9 (22.6, 46.6)
Ukraine Lower-middle Rivne and Khmelnytsky Provinces[g] EUROCAT [61] 2005–2011 7.0 (5.9, 8.2) 9.0 (7.8, 10.4) 1.7 (1.2, 2.4) 17.7 (16.0, 19.6)
United Kingdom High East Midlands and South Yorkshire EUROCAT [61] 2003–2012 4.9 (4.4, 5.5) 5.3 (4.8, 5.9) 1.0 (0.8, 1.3) 11.3 (10.5, 12.1)
United Kingdom High Glasgow EUROCAT [61] 1990–2000 6.8 (5.4, 8.4) 7.8 (6.3, 9.6) 2.4 (1.6, 3.4) 16.9 (14.7, 19.4)
United Kingdom High Merseyside and Chesire EUROCAT [61] 1995–1999 5.4 (4.2, 6.7) 6.5 (5.2, 8.0) 1.1 (0.6, 1.8) 12.9 (11.1, 15.0)
United Kingdom High North West Thames EUROCAT [61] 2003–2004 5.0 (3.7, 6.6) 4.7 (3.4, 6.3) 1.2 (0.6, 2.1) 10.9 (8.9, 13.2)
United Kingdom High Northern England EUROCAT [61] 2003–2012 5.8 (5.0, 6.6) 6.5 (5.6, 7.4) 1.6 (1.2, 2.1) 13.8 (12.6, 15.1)
United Kingdom High South West England EUROCAT [61] 2005–2012 4.2 (3.6, 4.9) 5.2 (4.5, 6.0) 1.2 (0.9, 1.6) 10.7 (9.7, 11.7)
United Kingdom High Thames Valley EUROCAT [61] 2003–2012 4.9 (4.1, 5.8) 4.8 (4.0, 5.8) 1.1 (0.7, 1.6) 10.8 (9.6, 12.1)
United Kingdom High Wales EUROCAT [61] 2003–2012 5.1 (4.4, 5.9) 6.4 (5.6, 7.3) 2.0 (1.5, 2.5) 13.5 (12.3, 14.8)
United Kingdom High Wessex EUROCAT [61] 2003–2012 5.9 (5.1, 6.9) 4.8 (4.0, 5.7) 1.0 (0.6, 1.4) 11.7 (10.5, 13.0)
AMERICAS
Argentina Upper-middle National Groisman B, et al.[74] November 2009–June 2012 3.6 (2.9, 4.3) 6.4 (5.5, 7.7) 1.9 (1.5, 2.5) 11.9 (10.7, 13.2)
Argentina Upper-middle Multi-Regional Lopez-Camelo JS, et al.[75] 2005–2007 3.7 (2.7, 4.6) 6.6 (5.3, 7.9) 2.0 (1.3, 2.8) 12.2 (10.5, 14.0)
Brazil Upper-middle National Orioli IM, et al.[76] 2006 1.4 (1.3, 1.5) 1.4 (1.3, 1.5)
Brazil Upper-middle Multi-Regional Lopez-Camelo JS, et al. [75] July 2005–December 2007 6.9 (5.2, 8.6) 14.2 (11.8, 16.6) 3.2 (2.1, 4.4) 24.3 (21.2, 27.5)
Canada High National ICBDSR 2011 Report [38] 2005–2009 1.0 (0.9, 1.2) 3.0 (2.7, 3.2) 0.7 (0.6, 0.8) 4.6 (4.3, 5.0)
Chile High Bio Bio, Los Lagos, Los Rios, Maule, Santiago Metropolitan, O'Higgins, Tarapaca, and Valparaiso Regions Nazer J and Cifuentes L [77] 2001–2010 3.7 (3.0, 4.4) 4.5 (3.7, 5.3) 1.7 (1.2, 2.1) 9.6 (8.5, 10.7)
Chile High Multi-Regional Lopez-Camelo JS, et al.[75] 2001–2007 3.7 (2.9, 4.4) 4.6 (3.8, 5.5) 1.8 (1.3, 2.3) 10.1 (8.8, 11.3)
Colombia Upper-middle Cali Pachajoa H, et al.[78] March 2004–October 2008 6.4 (3.9, 9.7) 7.3 (4.7, 10.8) 3.0 (1.5, 5.6) 16.7 (12.3, 21.1)
Colombia Upper-middle Bogota, Ubate, and Manizales Zarante I, et al.[79] April 2001–January 2008 11.0 (8.2, 13.8)
Colombia Upper-middle Bogota ICBDSR 2011 Report [38] 2009 1.6 (0.5, 3.8) 2.0 (0.7, 4.3) 0.0 (0.0, 1.2) 3.6 (1.8, 6.5)
Colombia Upper-middle Baraya, Garzon, Neiva, and Palermo Ostos H, et al.[80] 1998 9.6 (3.9, 19.8) 9.6 (3.9, 19.8) 1.4 (0.0, 7.7) 20.6 (11.5, 34.0)
Costa Rica Upper-middle National de la Paz Barboza-Arguello M, et al.[81] 2003–2012 4.8 (4.3, 5.3)
Cuba Upper-middle National ICBDSR 2011 Report [38] 2005–2009 3.8 (3.3, 4.3) 4.4 (3.9, 5.0) 1.7 (1.4, 2.1) 10.0 (9.2, 10.8)
Ecuador Upper-middle Multi-Regional Gonzalez-Andrade F and Lopez-Pulles R [82] 2001–2007 0.3 (0.3, 0.4) 2.5 (2.3, 2.7) 0.5 (0.4, 0.6) 3.3 (3.1, 3.5)
Guatemala Lower-middle National Acevedo CR, et al.[83] 2001–2003 2.3 (1.7, 2.9) 22.7 (20.8, 24.6) 3.0 (2.3, 3.7) 27.9 (25.8, 30.0)
Honduras Lower-middle Tegucigalpa Hernandez R and Alvarenga R [84] July 1998–September 2000 11.9 (8.2, 15.5)
Mexico Upper-middle Monterrey, Nuevo Leon Hernandez-Herrera RJ, et al.[85] 1995–1999 6.5 (5.1, 7.9) 8.2 (6.6, 9.7) 1.3 (0.8, 2.1) 16.0 (13.9, 18.2)
Mexico Upper-middle Guadalajara Alfaro N, et al.[86] 1988–1999 9.5 (8.0, 10.9) 10.3 (8.8, 11.8) 19.7 (17.6, 21.8)
Mexico Upper-middle National Navarrete Hernandez E, et al.[87] 2009–2010 2.1 (1.9, 2.2) 1.2 (1.1, 1.3) 3.3 (3.1, 3.5)
Mexico Upper-middle National ICBDSR 2011 Report [38] 2005–2009 4.6 (3.3, 5.9) 5.8 (4.3, 7.2) 1.6 (0.9, 2.5) 11.9 (9.8, 14.1)
Peru Upper-middle Lima Sanabria Rojas HA, et al.[88] 2006–2010 1.9 (1.1, 3.1) 6.1[a] (4.5, 7.8) 0.1 (0, 0.6) 8.2[a] (6.3, 10.0)
Uruguay Upper-middle Montevideo Castilla EE, et al.[89] 1999–2001 17.5 (11.9, 23.1)
United States High National Canfield MA, et al.[90] 1999–2007 1.3 (1.2, 1.4) 3.2 (3.1, 3.3) 0.8 (0.7, 0.8) 5.3 (5.1, 5.4)
Venezuela Upper-middle Maracaibo, Coro, and Ciudad Bolivar Castilla EE, et al.[89] 2000–2001 14.9 (11.0, 18.8)
SOUTH-EAST ASIA
Bangladesh Low Dhaka Dey AC, et al.[91] August 2006–July 2007 13.8 (9.2, 20.0)
India Lower-middle Kolkata Sarkar S, et al.[92] September 2011–August 2012 1.6 (0.2, 5.6) 14.0 (8.3, 22.1) 2.3 (0.5, 6.8) 17.8 (11.3, 26.8)
India Lower-middle Delhi Sood M, et al.[93] January 1988–August 1990 39.0 (26.3, 51.8) 26.0 (16.7, 38.7) 1.1 (0.0, 6.0) 66.2 (49.7, 82.8)
India Lower-middle Lucknow Sharma AK, et al.[94] 1982–1991 19.2 (16.8, 21.6) 19.6[e] (17.2, 22.0) 38.8[d] (35.4, 42.2)
India Lower-middle Pondicherry Mahadevan B and Bhat BV [95] July 1998–June 2004 18.0 (14.5, 21.6) 31.0 (26.3, 35.7) 7.0 (4.8, 9.2) 55.5[a] (49.3, 61.8)
India Lower-middle Duragpur Duttachoudhury A and Pal SK [96] January 1991 -December 1993 5.5 (1.5, 14.1) 5.5 (1.5, 14.1) 11.0 (4.8, 21.8)
India Lower-middle Erode Ponne S and Lakshmi UK [97] 2000–2004 10.7 (6.6, 12.7) 14.7 (12.3, 17.2) 1.9 (1.1, 2.8) 27.4 (24.1, 30.7)
India Lower-middle Himachal Pradesh Shimla Grover N [98] January 1991–December 1995 20.8 (12.9, 31.8) 16.8 (9.8, 27.0) 6.9 (2.8, 14.3) 44.6 (31.6, 57.5)
India Lower-middle Multi-Regional ICBDSR 2011 Report [38] 2005–2009 12.3 (11.4, 13.1) 11.0 (10.2, 11.8) 3.6 (3.1, 4.0) 26.8 (25.6, 28.1)
India Lower-middle Sevagram, Wardha Taksande A, et al.[99] January 2005–July 2007 5.3 (1.7, 12.4) 2.1 (0.3, 7.7) 7.5 (3.0, 15.4)
Nepal Low Thapathali Malla BK [100] 2004 5.3 (2.4, 10.1) 4.7 (2.0, 9.3) 1.8 (0.4, 5.2) 11.8 (7.2, 18.2)
Thailand Upper-middle Songkhla, Phatthalung, and Trang Provinces Jaruratanasirikul S, et al.[101] January 2001–December 2012 0.8 (0.4, 1.4) 0.7 (0.4, 1.3) 0.3 (0.1, 0.8) 1.9 (1.3, 2.7)
Thailand Upper-middle Chiang Mai Kitisomprayoonkul N and Tongsong T [102] June 1989–May 2000 5.6 (3.9, 7.4) 0.6 (0.2, 1.5) 0.4 (0.1, 1.3) 6.6 (4.7, 8.6)
Thailand Upper-middle Bangkok Wasant P and Sathienkijkanchai A [103] 1990–1999 2.6 (1.8, 3.4) 3.2 (2.4, 4.1) 0.8 (0.5, 1.4) 6.7[b, d] (5.5, 7.9)
WESTERN PACIFIC
Australia High South Australia Flood L, et al.[104] 2010 19.5 (13.4, 25.6)
Australia High Victoria, West Australia, South Australia, New South Wales, Queensland States Macaldowie A and Hilder L [105] 2006–2008 8.8 (8.2, 9.4)
China Upper-middle Hainan Province Fan L, et al.[106] 2010 5.8 (3.9, 7.7)
China Upper-middle Shenzhen City Yang M, et al.[107] 2003–2009 5.7 (4.6, 6.8)
China Upper-middle National Li X, et al.[108] 2006–2008 5.9 (5.6, 6.2) 6.0 (5.7, 6.3) 2.2 (2.0, 2.3) 14.0 (13.4, 14.5)
Northern China 6.8 (6.4, 7.3) 9.2 (8.6, 9.8) 2.7 (2.4, 3.0) 18.7 (17.9, 19.5)
Southern China 5.0 (4.6, 5.4) 3.1 (2.8, 3.4) 1.7 (1.5, 1.9) 9.7 (9.1, 10.3)
China Upper-middle Inner Mongolia Zhang X, et al.[109] 2005–2008 6.9 (4.8, 9.0) 10.6 (8.1, 13.2) 2.7 (1.4, 4.0) 20.3[f] (16.8, 23.8)
China Upper-middle National Dai L, et al. [110] 2009 6.5 (6.1, 6.9)
China Upper-middle Zhejiang Province Zhang XH, et al.[111] 2007–2009 6.3 (5.7, 7.0) 3.6 (3.1, 4.1) 1.4 (1.1, 1.7) 11.3 (10.4, 12.2)
China Upper-middle Luliang Prefecture, Shanxi Province Chen G, et al.[112] 2004–2005 82.6 (60.5, 104.7) 38.9 (25.2, 57.5) 26.5 (15.4, 42.4) 199.4[d] (165.2, 233.6)
China Upper-middle Beijing Li Y, et al.[113] January 2003–March 2009 0.0 (0.0, 0.6) 0.3 (0.0, 1.2) 0.3 (0.0, 1.2)
China Upper-middle Guizhou Province Liu J, et al. [114] Januray 1996–December 2004 4.2 (2.9, 5.5) 5.9 (4.4, 7.4) 0.7 (0.3, 1.4) 12.2[d] (10.0, 14.4)
China Upper-middle Gansu Province Cheng N, et al.[115] January 2001–January 2002 66.5 (46.9, 86.1)
China High Taiwan Chen BY, et al.[116] 2002 1.1 (0.7, 1.6) 1.1 (0.7, 1.6) 0.4 (0.2, 0.7) 2.5 (1.9, 3.1)
Japan High Osaka City Imaizumi Y, et al.[117] 1981–1990 7.1 (4.2, 11.4) 1.3 (0.3, 3.7) 8.4 (5.1, 12.9)
Japan High Ishikawa Prefecture Seto T, et al.[118] 1981–2000 0.8 (0.2, 1.3) 0.9 (0.3, 1.5) 1.0 (0.3, 1.6) 2.6 (1.7, 3.9)
Japan High National ICBDSR 2011 Report [38] 2005–2009 0.9 (0.6, 1.2) 5.2 (4.5, 5.9) 0.8 (0.5, 1.1) 6.9 (6.1, 7.7)
South Korea High National Kim MA, et al.[119] 2005–2006 0.2 (0.1, 0.3) 2.6 (2.2, 2.9) 0.3 (0.2, 0.4) 3.1 (2.7, 3.5)
Malaysia Upper-middle National Boo NY, et al.[120] 2009 2.1 (1.5, 2.6) 1.6 (1.1, 2.1) 0.8 (0.5, 1.2) 5.4 (4.5, 6.2)
New Zealand High National ICBDSR 2011 Report [38] 2005–2009 0.4 (0.2, 0.6) 2.1 (1.6, 2.6) 0.5 (0.3, 0.8) 3.0 (2.4, 3.6)
Papua New Guinea Lower-middle Port Moresby Dryden R [121] 1985–1986 3.0 (0.6, 8.8) 4.0 (1.1, 10.2) 7.0 (2.6, 14.4)
Singapore High National Shi LM, et al.[122] 1994–1998 0.5[b] (0.3, 0.9) 0.7 (0.4, 1.1) 1.2[b] (0.8, 1.8)
Vietnam Lower-middle Binh Thuan Province Hoang T, et al.[123] 2010 3.6 (1.2, 8.4) 0.0 (0.0, 2.6) 0.7 (0.0, 4.0) 4.3 (1.6, 9.4)
UNCLASSIFIED
Palestine East Jerusalem and Southern West Bank Dudin A [124] 1986–1993 54.9[a] (46.1, 63.7)

a Non-NTDs such as syndromes, chromosomal abnormalities, and spina bifida occulta were not included in our calculations

b May include non-NTDs, but could not stratify in our calculation

c Referred cases were not included in our calculation

d Individual NTDs do not sum to total NTDs (e.g., only isolated NTD counts were provided, but prevalence includes multiple NTDs)

e Spina bifida cases included encephalocele

f Recalculated NTD prevalence was inconsistent with the original authors’ published rate

g Regions may be impacted by Chernobyl disaster

N/A = Not applicable

* If prevalence cell is blank, data were either not reported, not stratified by specific type of NTD, or unclear

¥ Sum of all NTDs reported, which includes spina bifida and/or anencephaly and encephalocele, depending on what NTDs the authors of the original study assessed

Fig 2. Neural Tube Defects Prevalence and Confidence Intervals by World Bank Income Classifications (Log Scale)[18].

Fig 2

Furthermore, we observed that among studies that reported stratified data for all three types of NTDs, on average, spina bifida attributed the highest percentage to total NTD prevalence, followed by anencephaly and then encephalocele (Fig 3). When stratified by country income level, we noticed a general decrease in the median prevalence for each specific type of NTD from the lower-middle to high income countries (Fig 4). NTD prevalence estimates by WHO region are as follows:

Fig 3. Percent of all Neural Tube Defects (NTDs) Attributable to Each Condition for Studies that Reported all Three Types of NTDs: Anencephaly, Spina Bifida, and Encephalocele.

Fig 3

Bars Indicate the Median Percent for Each Condition.

Fig 4. Prevalence per 10,000 Births for Specific Types of Neural Tube Defects by World Bank Income Classifications [18].

Fig 4

Bars Indicate the Median Prevalence for Each Condition.

African Region: Data from eight of 47 WHO member countries, represented by 11 studies, met our inclusion criteria (Fig 5). The lowest reported NTD prevalence for the region was reported in Nigeria (5.2 per 10,000 births) [24] and the highest was reported in Algeria (75.4 per 10,000 births) [19]. The median NTD prevalence was 11.7 per 10,000 births. Data from this region were primarily gathered from hospital-based retrospective case reviews.

Fig 5. African Region Neural Tube Defects Prevalence Estimates (Location, Number of Hospitals).

Fig 5

If there were national data available for more than one NTD, the entire country was filled-in based on the prevalence per 10,000 births. In instances where multiple prevalence estimates were available at the national level, the prevalence reported by the study/report with the least risk-of-bias was selected. Countries colored in grey are not a part of the World Health Organization region. Shapefile reprinted from http://www.diva-gis.org under a CC BY license, with permission from DIVA-GIS and Dr. Robert Hijmans.

Eastern Mediterranean Region: Published data were available for 12 of the 21 countries in the region and were represented by 31 studies (Fig 6). This region exhibited variability in reported NTD prevalence as well, with estimates as low as 2.1 per 10,000 births in the United Arab Emirates [60] and as high as 124.1 per 10,000 births in Swat, Pakistan [48]. This region had the highest median prevalence (21.9 per 10,000 births). Elevated NTD prevalence estimates were consistently observed in Pakistan. All five studies in Pakistan reported estimates between 38.6 and 124.1 per 10,000 births [4852].

Fig 6. Eastern Mediterranean Region Neural Tube Defects Prevalence Estimates (Location, Number of Hospitals).

Fig 6

If there were national data available for more than one NTD, the entire country was filled-in based on the prevalence per 10,000 births. In instances where multiple prevalence estimates were available at the national level, the prevalence reported by the study/report with the least risk-of-bias was selected. Countries colored in grey are not a part of the World Health Organization region. Shapefile reprinted from http://www.diva-gis.org under a CC BY license, with permission from DIVA-GIS and Dr. Robert Hijmans.

European Region: We identified a total of 60 different studies/reports spanning a total of 26 countries of the 53 countries in the region (Fig 7). Ninety-five percent of NTD data from Europe came from regional or national registries/surveillance systems. The reported NTD prevalence estimates in this region were relatively less variable than other regions (range: 1.3–35.9 per 10,000 births) [61, 70]. The median for the European region was 9.0 per 10,000 births.

Fig 7. European Region Neural Tube Defects Prevalence Estimates (Location, Number of Hospitals).

Fig 7

The majority of data from the European region was population based. All data based on hospital studies from regions is indicated with the number of hospitals. If there were national or regional data available for more than one NTD, the entire country or region was filled-in based on the prevalence per 10,000 births. In instances where multiple prevalence estimates were available at the national level, the prevalence reported by the study/report with the least risk-of-bias was selected. Countries colored in grey are not a part of the World Health Organization region. A national study from Israel is not represented on this map since it only provided prevalence by ethnicity. Shapefile reprinted from http://www.gadm.org under a CC BY license, with permission from Global Administrative Areas and Dr. Robert Hijmans.

Americas Region: Data from 21 studies/reports representing 15 of the 35 countries were available (Fig 8). This region had the least variability in reported NTD prevalence estimates. Among studies that included spina bifida and at least one other NTD, the lowest prevalence was 3.3 per 10,000 births [82, 87]. A study from Brazil which only counted spina bifida reported a prevalence of 1.4 per 10,000 births [75]. In this region, the highest prevalence was reported in Guatemala (27.9 per 10,000 births) [83]. The median prevalence was 11.5 per 10,000 births.

Fig 8. American Region Neural Tube Defects Prevalence Estimates (Location, Number of Hospitals).

Fig 8

If there were national data available for more than one NTD, the entire country was filled-in based on the prevalence per 10,000 births. In instances where multiple prevalence estimates were available at the national level, the prevalence reported by the study/report with the least risk-of-bias was selected. Shapefile reprinted from http://www.diva-gis.org under a CC BY license, with permission from DIVA-GIS and Dr. Robert Hijmans.

South-East Asian Region: There were 14 studies representing four of the 11 countries in South-East Asia (Fig 9). The lowest prevalence estimate for the region was 1.9 per 10,000 births in Thailand [101] and the highest was 66.2 per 10,000 births in India [93]. Most of the data for this region came from either Thailand or India; three and nine studies, respectively. The median prevalence in this region was 15.8 per 10,000 births.

Fig 9. South-East Asian Region Neural Tube Defects Prevalence Estimates (Location, Number of Hospitals).

Fig 9

If there were national data available for more than one NTD, the entire country was filled-in based on the prevalence per 10,000 births. In instances where multiple prevalence estimates were available at the national level, the prevalence reported by the study/report with the least risk-of-bias was selected. North Korea had no reported data and was not shown in map due to scaling considerations. Shapefile reprinted from http://www.diva-gis.org under a CC BY license, with permission from DIVA-GIS and Dr. Robert Hijmans.

Western Pacific Region: Of the 27 countries, data were available for nine countries from 22 studies/reports (Fig 10). This region had the lowest median prevalence value (6.9 per 10,000 births). As stated previously, China exhibited the greatest variability in reported NTD prevalence estimates (range: 0.3–199.4 per 10,000 births) [113, 112]. As seen in Li et al., NTD estimates tend to be higher in northern China (18.7 per 10,000 births) than in the southern part of the country (9.7 per 10,000 births) [108]. When excluding data from China, reported NTD prevalence in this region ranged from as low as 1.2 per 10,000 births in Singapore [122] to as high as 19.5 per 10,000 births in Australia [104].

Fig 10. Western Pacific Region Neural Tube Defects Prevalence Estimates (Location, Number of Hospitals).

Fig 10

If there were national data available for more than one NTD, the entire country was filled-in based on the prevalence per 10,000 births. In instances where multiple prevalence estimates were available at the national level, the prevalence reported by the study/report with the least risk-of-bias was selected. Countries colored in grey are not a part of the World Health Organization region. Shapefile reprinted from http://www.diva-gis.org under a CC BY license, with permission from DIVA-GIS and Dr. Robert Hijmans.

Surveillance System/Registry Coverage

Fig 11 shows the types of NTD data collection worldwide, categorized as national surveillance system/registry, regional surveillance system/registry, or other (i.e., no surveillance system/registry but has data collected using another methodology). The map illustrates that there are limited amounts of data derived from surveillance/registry programs in countries in the African (1/8) and South-East Asian (2/4) regions. In contrast, the Americas (11/15) and European (26/26) countries had higher utilization of surveillance/registries. Furthermore, the presence of a NTD surveillance system/registry increased with country income status: low income (0%), lower-middle (25%), upper-middle (70%), and high income (91%).

Fig 11. Data Source: Surveillance/Registry Coverage by Geographic Level.

Fig 11

Shapefile reprinted from http://www.diva-gis.org under a CC BY license, with permission from DIVA-GIS and Dr. Robert Hijmans.

Risk-of-Bias (RoB)

The RoB evaluation generated scores ranging from 0.0 to 14.0 (possible range 0.0 to 18.0), with lower scores indicating lower RoB. When average RoB scores were classified by WHO region, studies/reports from Europe had the lowest (5.0), while studies/reports from the Eastern Mediterranean (10.9), South-East Asian (11.3) and African (11.5) regions had the highest RoB scores (Fig 12). In addition, we observed an inverse relationship between RoB score and country income level. As the income level of countries increased, their average RoB scores decreased (Fig 13).

Fig 12. Average Study Risk-of-Bias by World Health Organization Region.

Fig 12

Fig 13. Average Study Risk-of-Bias by World Bank Income Classification [18].

Fig 13

Discussion

Our review provides a comprehensive global assessment of NTD prevalence as observed from 75 countries at the national, regional, or local levels, which represents about 40% of the total number of WHO member states (194) [125]. The African and South-East Asian regions have minimal data available, demonstrating the need to establish surveillance and other mechanisms that can provide countries with standardized data to better determine the burden of birth defects in general, and NTDs in particular. More complete ascertainment of data will be useful in determining country level needs for prevention of NTDs, monitoring trends through time, helping to evaluate the impact of prevention efforts, and developing services for those affected.

Overall, reported prevalence estimates varied greatly between, and also, within countries ranging from 0.3 to 199.4 NTDs per 10,000 births. Through the RoB assessment, we discovered this may be in part due to variation in data collection methodology among individual studies. For example, both studies from post-fortification Brazil had a 10-fold difference in spina bifida prevalence estimates: 1.4 per 10,000 live births (95% CI: 1.2, 1.5) in the Orioli et al. study [76] and 14.2 per 10,000 births (95% CI: 11.8, 16.6) in the Lopez-Camelo et al. study [75]. Orioli et al. assessed spina bifida prevalence in 2006 in a population-based cross-sectional study that included millions of live births from the Live Births Information System. The system used to estimate NTDs in the Orioli et al. paper had some limitations with case ascertainment, case definition, and lack of standardized diagnoses that may impact the validity and reliability of the estimates [76, 126]. The Lopez-Camelo et al. study used data from the Latin American Collaborative Study of Congenital Anomalies (ECLAMC) which is a hospital-based, voluntary birth defects surveillance network that includes 19 hospitals throughout Brazil. It is important to note that the NTD prevalence variability we found in our review could also be true differences, resulting from other factors including nutritional factors, genetics, routine folic acid supplementation, and the presence of folic acid fortification programs [127129].

By conducting our RoB assessment, we found that case ascertainment methods and data quality varied greatly among studies. Therefore, the prevalence estimates from different studies are not directly comparable nor can they be used to calculate a combined estimate [130]. For example, the scope of studies varied from single-hospital studies done over the span of one year to studies using established nationally representative surveillance systems. In addition, many studies did not clearly define NTDs or provide inclusion criteria (e.g., gestational age and birth outcome). While we attempted to re-calculate reported prevalence to match our definition (e.g., removing chromosomal NTDs and spina bifida occulta), many times this was not possible because data were not stratified by type of NTD. Standardized protocols (i.e., case definitions, inclusion criteria, variables collected, reporting) for birth defects surveillance would allow better comparison among studies. In addition, improved methodology can make prevalence estimates more accurate. For example, including cases among pregnancies terminated for fetal anomalies, especially in countries where this is legal, usually leads to higher and more accurate prevalence estimates due to better case ascertainment. Recently, standardized tools for birth defects surveillance have been developed through a collaborative effort of health organizations including WHO, CDC, and ICBDSR. The Birth Defects Surveillance Manual and Atlas of Selected Congenital Anomalies are available in three languages (English, Spanish, and French) and have been developed specifically for low and middle income countries [131, 132].

In our review, although some data were available from low and middle income countries, most of the data were not derived from surveillance systems or registries. Often data from these countries were collected in limited geographic areas (single hospital studies), were not population-based, and lacked well defined procedures for collecting birth defects data. NTD prevalence data from surveillance systems and registries, such as EUROCAT, that used standardized and more comprehensive case ascertainment protocols (e.g., reporting cases from termination of pregnancy where it is legal) and had greater geographic and population coverage are more likely to estimate the true burden of NTDs in those regions more accurately.

This review advances the state of knowledge in three ways: first, this is the most current systematic review on global NTD prevalence; second, this review was able to identify large gaps in data collection and highlight international differences; and third, through the RoB assessment this study was able to document the wide variation in the quality and methodology of current reports. Our review supports the findings of previously published literature and demonstrates there is a high burden of NTDs globally. However, our review purposefully does not model data to non-reporting regions in an effort to highlight the lack of data globally. Moreover, it expands the scope of previously published systematic reviews that only included studies/reports from countries in one region or select income levels.

Limitations

Beyond issues related to the abstracted data and study-specific methodologic issues, our review is also limited by factors related to our search criteria. Since this review only searched English and Spanish literature and excluded studies with small study populations, it may not have incorporated all relevant NTD prevalence information. In select studies, our review was unable to report prevalence estimates for each specific type of NTD since individual values were not always stratified. Lastly, presence of birth outcome data (i.e., live birth, stillbirth, and termination of pregnancy) was only used for the RoB analysis. Ideally, prevalence data should be stratified by birth outcome, however, many studies did not describe the birth outcome in sufficient detail (i.e., whether it was in the numerator, denominator, or both) or at all.

Conclusions

This review describes the available data on the current burden of NTDs throughout the world. Despite methodological variations and coverage gaps in data collection, high NTD prevalence estimates throughout the literature indicate that NTDs remain an important preventable public health problem. This review provides a snapshot of areas in need of greater coverage and quality of NTD monitoring and surveillance and identifies opportunities for development such as standard reporting of birth defects as recommended by the World Health Assembly resolution. More importantly, regions that include large portions of the global population (e.g., South-East Asia) are lacking surveillance/registry data and case ascertainment methods that include all birth outcomes which provide the most reliable and valid estimates. In response to this need, CDC’s Birth Defects COUNT global initiative is working with partners in South-East Asia, East and Central Africa, and Latin America to implement and improve surveillance of NTDs as well as other birth defects [133].

Supporting Information

S1 Document. PRISMA Checklist.

(DOC)

S2 Document. Permission to publish map shapefiles.

(DOCX)

Acknowledgments

We would like to thank Barbara Landreth, CDC librarian, for her assistance with the literature search. We would also like to thank Csaba Siffel, Cho-Hee Schrader, and Chelsey Brack for their assistance in abstract review. Finally, we would like to thank Diana Valencia for her assistance in abstracting data recorded in Spanish.

Disclaimer: The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

Data Availability

All relevant data are within the paper and its Supporting Information files.

Funding Statement

AS, IZ, and BLT were supported in part by an appointment to the Research Participation Program at the CDC administered by the Oak Ridge Institute for Science and Education (ORISE). The commercial company, Carter Consulting Inc., provided support in the form of salaries for authors [HR, JM]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Associated Data

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Supplementary Materials

S1 Document. PRISMA Checklist.

(DOC)

S2 Document. Permission to publish map shapefiles.

(DOCX)

Data Availability Statement

All relevant data are within the paper and its Supporting Information files.


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