Literature DB >> 27064786

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

Ibrahim Zaganjor1, Ahlia Sekkarie1, Becky L Tsang1, Jennifer Williams1, Hilda Razzaghi1,2, Joseph Mulinare1,2, Joseph E Sniezek1, Michael J Cannon1, Jorge Rosenthal1.   

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.

Entities:  

Mesh:

Year:  2016        PMID: 27064786      PMCID: PMC4827875          DOI: 10.1371/journal.pone.0151586

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


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 [13-15]. 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.

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) [19-124]. 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*.

CountryWorld Bank ClassificationLocationAuthorYear(s) IncludedPrevalence Rate per 10,000 Births
AnencephalySpina bifidaEncephaloceleSum of Reported NTDs¥
Prevalence95% CIPrevalence95% CIPrevalence95% CIPrevalence95% CI
AFRICA
AlgeriaUpper-middleSetifHoucher, et al.[19]2004–200632.2(25.6, 38.8)42.8[f](35.2, 50.4)0.3(0.0, 2.0)75.4(65.4, 85.4)
CameroonLower-middleYaoundeNjamnshi AK, et al.[20]January 1997- December 200618.6(14.9, 22.3)
Democratic Republic of CongoLowNyankunde, Oriental ProvinceAhuka OL, et al.[21]January 1993–August 20011.1(0.0, 6.3)6.8(2.5, 14.8)2.3(0.3, 8.2)10.2(4.7, 19.4)
GhanaLower-middleAccraAnyebuno M, et al.[22]January 1991–December 19928.4(4.8, 13.6)3.1(1.2, 6.8)11.5(7.2, 17.4)
MalawiLowBlantyreMsamati BC, et al.[23]1998–19996.3(3.6, 10.2)6.3(3.6, 10.2)
NigeriaLower-middleCross River and Akwa Ibom StatesEkanem TB, et al.[24]1980–20031.6(1.0, 2.4)3.7(2.7, 4.8)5.2(4.0, 6.5)
NigeriaLower-middleJosAirede KI [25]June 1987–June 19903.3(0.4, 12.1)41.8(27.1, 61.7)13.4(5.8, 26.4)58.6[a](39.3, 78.0)
South AfricaUpper-middleEastern Cape, Kwazulu Natal, Mpumalanga, and Free State ProvincesSayed AR, et al.[26]October 2004–June 20053.7(2.2, 5.9)5.4(3.5, 8.0)9.8(6.9, 12.7)
South AfricaUpper-middleSovenga, Northern TransvaalVenter PA, et al.[27]June 1989–December 199217.1(9.1, 29.2)15.8(8.1, 27.5)2.6(0.3, 9.5)35.4(23.4, 51.6)
South AfricaUpper-middleCape TownViljoen DL, et al. [28]1973–199211.7(10.8, 12.6)
TanzaniaLowDar es SalaamKinasha AD and Manji K [29]2000–20021.2(0.3, 3.0)26.1(20.7, 31.5)2.9(1.4, 5.4)30.2(24.4, 36.0)
EASTERN MEDITERRANEAN
EgyptLower-middleUpper EgyptMohammed YA, et al.[30]March 2007–October 20072.0(0.1, 11.1)10.0(3.3, 23.3)4.0(0.5, 14.5)16.0[b](6.9, 31.5)
IranUpper-middleYasuj, South West IranEbrahimi S, et al.[31]March 2008–February 201138.1(24.9, 51.3)
IranUpper-middleAhvazBehrooz AG and Gorjizadeh MH [32]March 2002–March 200424.9(16.4, 33.4)15.1(9.2, 23.3)2.3(0.5, 6.6)42.2(31.2, 53.3)
IranUpper-middleGorgan, GolestanAbdollahi Z, et al.[33]December 2007–December 200821.9N/A
IranUpper-middleTehranDelshad S, et al.[34]March 2005-March 20078.5(6.2, 10.8)1.6(0.8, 3.0)10.1(7.6, 12.7)
IranUpper-middleBirjandAfshar M, et al.[35]April 1997–December 200115.5(10.1, 22.7)8.9(5.0, 14.7)1.8(0.4, 5.2)29.8(21.6, 38.0)
IranUpper-middleUrmiaRad IA, et al.[36]January 2001–June 200555.2(43.0, 67.5)24.8(16.6, 33.0)2.8(0.8, 7.3)82.9(67.9, 97.8)
IranUpper-middleHamadan ProvinceFarhud DD, et al.[37]1991–199715.6(8.1, 25.9)7.0(2.6, 15.2)50.1(35.2, 65.0)
IranUpper-middleTabrizICBDSR 2011 Report [38]20094.7(2.4, 8.5)0.9(0.1, 3.1)0.9(0.1, 3.1)6.5(3.6, 10.7)
IraqUpper-middleAl-Ramadi, Al-Anbar GovernateAl-Ani ZR, et al.[39]October 2010 –October 20113.5(0.4, 12.6)15.7(7.2, 29.8)8.7(2.8, 20.3)27.9[a](15.9, 45.2)
IraqUpper-middleBasrahAl-Sadoon I, et al.[40]19902.5(0.5, 7.2)7.4(3.4, 14.1)9.9(5.1, 17.2)
JordanUpper-middleNorth JordanAmarin ZO and Obeidat AZ [41]2005–20069.5(5.5, 15.5)
JordanUpper-middleAmmanAqrabawi HE [42]April 2002 –April 20030.0(0.0, 7.3)59.0(37.9, 80.0)3.9(0.5, 14.2)62.9[a](41.2, 84.6)
JordanUpper-middleAmmanMasri AT [43]1993–20023.5[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)
JordanUpper-middleIrbid ProvinceDaoud AS, et al.[44]January 1991–December 19933.7(2.4, 5.0)10.0(7.9, 12.1)2.6(1.7, 4.0)16.4(13.7, 19.1)
KuwaitUpper-middleAl-Jahara RegionMadi SA, et al.[45]January 2000–December 20013.9(0.8, 11.3)2.6(0.3, 9.3)6.5(2.1, 15.1)
LibyaUpper-middleBenghaziSingh R and Al-Sudani O [46]19957.4(3.8, 13.0)0.6(0.0, 3.4)8.0(4.3, 13.7)
OmanHighNationalAlasfoor D and ElSayed MK [47]20106.8N/A23.2N/A
PakistanLower-middleSwatKhattak ST, et al.[48]Januray 2007–December 2007113.3(85.5, 141.1)7.2(2.0, 18.4)124.1[d](95.0, 153.2)
PakistanLower-middlePeshawarQazi G [49]Januray 2009–December 200947.2(30.3, 70.2)21.6(10.8, 38.7)68.8(46.1, 91.6)
PakistanLower-middleKarachiPerveen F and Tyyab S [50]January 2000–October 200529.4(17.2, 47.1)15.6(7.1, 29.6)5.2(1.1, 15.2)50.2(33.6, 72.1)
PakistanLower-middleLahoreNajmi RS [51]November 1994–October 1996; August 1997–March 199829.6(19.5, 39.7)17.0(10.3, 26.6)2.7(0.6, 7.9)49.3(36.3, 62.3)
PakistanLower-middleKarachiJooma R [52]200219.8(11.6, 30.0)15.7(8.5, 25.0)3.1(0.6, 8.9)38.6(26.4, 50.9)
QatarHighDohaBener A, et al.[53]January 1985–December 20093.6(2.9, 4.3)7.3(6.4, 8.4)10.9(9.7, 12.2)
Saudi ArabiaHighAl-KhobarAl-Jama F, et al.[54]January 1992–December 199722.4(14.8, 30.0)25.7(17.5, 33.9)5.4(2.3, 10.7)53.5(41.7, 65.3)
Saudi ArabiaHighAsir RegionAsindi A and Al-Shehri A.[55]January 1995–December 19980.4(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 ArabiaHighJeddahSafdar OY, et al.[56]2001–20057.6N/A
Saudi ArabiaHighAl-Madinah Al-MunawarahMurshid WR [57]April 1996–March 199710.9(6.5, 17.2)10.9(6.5, 17.2)
Saudi ArabiaHighRiyadhHakami WS and Majeed-Saidan MA [58]January 2001–December 20104.5(3.2, 5.9)
SudanLower-middleOmdurmanElsheikh GEA and Ibrahim SA [59]February 2003–January 200412.5(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 EmiratesHighNationalAl Hosani H, et al.[60]January 1999–December 20012.1[f](1.4, 2.8)
EUROPE
AustriaHighStyriaEUROCAT [61]2003–20091.7(0.9, 2.9)4.6(3.1, 6.4)1.5(0.8, 2.7)7.7(5.8, 10.0)
BelgiumHighAntwerpEUROCAT [61]2003–20122.6(2.0, 3.5)4.5(3.6, 5.5)0.8(0.5, 1.4)8.0(6.8, 9.3)
BelgiumHighHainautEUROCAT [61]2003–20123.2(2.3, 4.4)4.1(3.1, 5.4)1.2(0.7, 2.0)8.5(7.0, 10.3)
BulgariaUpper-middlePlevin RegionKovacheva K, et al.[62]1988–200620.2(16.2, 24.2)
CroatiaHighZagrebEUROCAT [61]2003–20122.0(1.1, 3.3)1.4(0.7, 2.6)1.1(0.5, 2.2)4.5(3.1, 6.4)
Czech RepublicHighNationalEUROCAT [61]2003–20102.4(2.1, 2.8)3.9(3.5, 4.3)1.3(1.0, 1.5)7.6(7.0, 8.2)
DenmarkHighNationalPasternak B, et al.[63]1997–20115.5(4.1, 6.8)
DenmarkHighOdenseEUROCAT [61]2003–20124.1(2.5, 6.2)5.8(3.9, 8.3)1.5(0.7, 3.1)11.4(8.7, 14.7)
FinlandHighNationalEUROCAT [61]2003–20113.2(2.7, 3.7)4.0(3.5, 4.6)1.9(1.5, 2.3)9.0(8.3, 9.9)
FranceHighBas-RhinStoll C, et al.[64]1979–20084.3[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)
FranceHighAuvergneEUROCAT [61]20022.2(0.4, 6.6)3.0(0.8, 7.7)3.0(0.8, 7.7)8.2(4.1, 14.7)
FranceHighFrench West IndiesEUROCAT [61]2009–20123.3(1.8, 5.6)4.0(2.3, 6.5)1.2(0.4, 2.8)8.5(6.0, 11.8)
FranceHighIle de la ReunionEUROCAT [61]2003–20127.3(6.0, 8.8)9.1(7.6, 10.8)2.0(1.3, 2.9)18.4(16.3, 20.7)
FranceHighParisEUROCAT [61]2003–20124.7(3.9, 5.6)5.1(4.3, 6.1)1.8(1.3, 2.4)11.6(10.3, 13.0)
GermanyHighNorthern Rhine RegionKlusmann A, et al.[65]January 1996 -December 20031.9(1.6, 2.2)4.4(3.9, 4.9)0.8(0.6, 1.0)7.1(6.5, 7.7)
GermanyHighMainzEUROCAT [61]2003–20113.8(1.9, 6.9)6.6(4.0, 10.4)3.5(1.7, 6.4)14.0(10.0, 19.0)
GermanyHighSaxony-AnhaltEUROCAT [61]2003–20122.0(1.4, 2.8)5.6(4.6, 6.9)1.4(0.9, 2.1)9.0(7.6, 10.5)
HungaryUpper-middleNationalICBDSR 2011 Report [38]2005–20092.0(1.6, 2.4)4.4(3.8, 5.0)0.6(0.4, 0.9)7.0(6.3, 7.7)
IrelandHighNationalMcDonnell R, et al.[66]2009–20114.7(3.8, 5.6)5.1(4.2, 6.0)0.7(0.4, 1.1)10.4(9.1, 11.8)
IrelandHighCork & KerryEUROCAT [61]2003–20124.9(3.6, 6.5)5.4(4.0, 7.0)1.0(0.5, 1.9)11.3(9.2, 13.6)
IrelandHighDublinEUROCAT [61]2003–20122.2(1.7, 2.9)3.0(2.4, 3.8)0.7(0.4, 1.1)5.9(5.0, 7.0)
IrelandHighSouth East IrelandEUROCAT [61]2003–20123.3(2.1, 4.9)5.0(3.6, 6.9)0.3(0.0, 1.0)8.6(6.6, 11.0)
IsraelHighNationalZlotogora J, et al.[67]2002–2004
Jews4.9N/A2.7N/A8.1N/A
Arabs and Druze8.2N/A6.2N/A16.7N/A
IsraelHighMulti-RegionalICBDSR 2011 Report [38]2005–20091.3(0.8, 1.8)2.9(2.2, 3.6)0.5(0.2, 0.9)4.6(3.7, 5.5)
ItalyHighEmilia RomagnaEUROCAT [61]2003–20122.2(1.7, 2.7)2.7(2.2, 3.3)0.7(0.5, 1.0)5.6(4.9, 6.4)
ItalyHighSicilyEUROCAT [61]2003–20040.5(0.1, 1.8)1.5(0.5, 3.3)0.0(0.0, 0.9)2.0(0.9, 3.9)
ItalyHighTuscanyEUROCAT [61]2003–20121.9(1.5, 2.5)3.1(2.5, 3.8)0.7(0.4, 1.1)5.7(4.9, 6.6)
ItalyHighCampaniaICBDSR 2011 Report [38]2005–20093.6(2.9, 4.2)3.1(2.5, 3.8)1.0(0.6, 1.3)7.7(6.7, 8.7)
ItalyHighLombardyICBDSR 2011 Report [38]20092.0(0.2, 7.1)2.0(0.2, 7.1)1.0(0.0, 5.5)4.9(1.6, 11.5)
ItalyHighNorth East ItalyICBDSR 2011 Report [38]2005–20091.5(1.0, 2.0)2.5(1.9, 3.1)0.5(0.2, 0.8)4.5(3.7, 5.3)
MaltaHighNationalEUROCAT [61]2003–20112.2(0.9, 4.3)6.3(4.0, 9.5)1.6(0.6, 3.6)10.2(7.2, 14.0)
NetherlandsHighNorthern NetherlandsEUROCAT [61]2003–20122.6(1.9, 3.5)4.6(3.7, 5.7)0.6(0.3, 1.0)7.7(6.5, 9.1)
NorwayHighNationalEUROCAT [61]2003–20123.5(3.0, 4.0)4.7(4.1, 5.2)0.9(0.7, 1.2)9.1(8.4, 9.9)
PolandHighNationalEUROCAT [61]2003–20100.8(0.7, 0.9)4.5(4.3, 4.8)0.6(0.5, 0.7)5.9(5.7, 6.2)
PolandHighWielkopolskaEUROCAT [61]2003–20101.2(0.8, 1.7)6.3(5.5, 7.3)1.0(0.7, 1.4)8.5(7.5, 9.6)
PortugalHighSouth PortugalEUROCAT [61]2003–20111.2(0.8, 1.9)1.8(1.2, 2.5)0.2(0.1, 0.6)3.2(2.4, 4.2)
RussiaHighArkhangelskaja OblastPetrova JG and Vaktskjold A [68]1995–200410.7(9.0, 12.4)10.4(8.7, 12.1)21.1(18.7, 23.5)
RussiaHighMoscowICBDSR 2011 Report [38]2005–20092.9(2.3, 3.5)3.7(3.0, 4.4)1.1(0.7, 1.4)7.6(6.6, 8.6)
Slovak RepublicHighMulti-RegionalICBDSR 2011 Report [38]2005–20090.9(0.6, 1.3)2.2(1.7, 2.8)0.7(0.4, 1.0)3.8(3.1, 4.5)
SpainHighBarcelonaEUROCAT [61]2003–20074.9(3.4, 6.8)3.3(2.1, 4.9)0.8(0.3, 1.8)9.0(7.0, 11.4)
SpainHighBasque CountryEUROCAT [61]2003–20115.2(4.2, 6.3)4.1(3.2, 5.2)0.7(0.4, 1.2)10.0(8.6, 11.5)
SpainHighNationalEUROCAT [61]2003–20120.3(0.2, 0.5)0.9(0.6, 1.1)0.2(0.1, 0.3)1.3(1.0, 1.6)
SpainHighValencia RegionEUROCAT [61]2007–20112.4(1.9, 3.1)2.4(1.9, 3.1)1.5(1.1, 2.1)6.4(5.5, 7.4)
SwedenHighNationalEUROCAT [61]2007–20112.8(2.4, 3.3)3.8(3.3, 4.3)1.0(0.7, 1.3)7.5(6.8, 8.3)
SwitzerlandHighNationalPoretti A, et al.[69]January 2001–December 20071.8[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)
SwitzerlandHighVaudEUROCAT [61]2003–20123.5(2.3, 5.2)4.5(3.1, 6.2)2.4(1.4, 3.7)10.4(8.2, 12.9)
TurkeyUpper-middleAfyonkarahisarOnrat ST, et al.[70]July 2003–December 200413.9(7.2, 24.3)19.7(11.5, 31.5)2.3(0.3, 8.4)35.9(23.3, 48.5)
TurkeyUpper-middleIzmirMandiracioglu A, et al.[71]January 2000–December 200014.3[a, b](10.4, 18.2)
TurkeyUpper-middleMulti-RegionalTuncbilek E, et al.[72]July 1993–June 199411.0(7.0, 16.3)13.2(8.4, 18.0)5.9(3.2, 10.2)30.1(22.9, 37.4)
TurkeyUpper-middleAnkaraHimmetoglu O, et al.[73]1988–199534.9(22.6, 46.6)
UkraineLower-middleRivne and Khmelnytsky Provinces[g]EUROCAT [61]2005–20117.0(5.9, 8.2)9.0(7.8, 10.4)1.7(1.2, 2.4)17.7(16.0, 19.6)
United KingdomHighEast Midlands and South YorkshireEUROCAT [61]2003–20124.9(4.4, 5.5)5.3(4.8, 5.9)1.0(0.8, 1.3)11.3(10.5, 12.1)
United KingdomHighGlasgowEUROCAT [61]1990–20006.8(5.4, 8.4)7.8(6.3, 9.6)2.4(1.6, 3.4)16.9(14.7, 19.4)
United KingdomHighMerseyside and ChesireEUROCAT [61]1995–19995.4(4.2, 6.7)6.5(5.2, 8.0)1.1(0.6, 1.8)12.9(11.1, 15.0)
United KingdomHighNorth West ThamesEUROCAT [61]2003–20045.0(3.7, 6.6)4.7(3.4, 6.3)1.2(0.6, 2.1)10.9(8.9, 13.2)
United KingdomHighNorthern EnglandEUROCAT [61]2003–20125.8(5.0, 6.6)6.5(5.6, 7.4)1.6(1.2, 2.1)13.8(12.6, 15.1)
United KingdomHighSouth West EnglandEUROCAT [61]2005–20124.2(3.6, 4.9)5.2(4.5, 6.0)1.2(0.9, 1.6)10.7(9.7, 11.7)
United KingdomHighThames ValleyEUROCAT [61]2003–20124.9(4.1, 5.8)4.8(4.0, 5.8)1.1(0.7, 1.6)10.8(9.6, 12.1)
United KingdomHighWalesEUROCAT [61]2003–20125.1(4.4, 5.9)6.4(5.6, 7.3)2.0(1.5, 2.5)13.5(12.3, 14.8)
United KingdomHighWessexEUROCAT [61]2003–20125.9(5.1, 6.9)4.8(4.0, 5.7)1.0(0.6, 1.4)11.7(10.5, 13.0)
AMERICAS
ArgentinaUpper-middleNationalGroisman B, et al.[74]November 2009–June 20123.6(2.9, 4.3)6.4(5.5, 7.7)1.9(1.5, 2.5)11.9(10.7, 13.2)
ArgentinaUpper-middleMulti-RegionalLopez-Camelo JS, et al.[75]2005–20073.7(2.7, 4.6)6.6(5.3, 7.9)2.0(1.3, 2.8)12.2(10.5, 14.0)
BrazilUpper-middleNationalOrioli IM, et al.[76]20061.4(1.3, 1.5)1.4(1.3, 1.5)
BrazilUpper-middleMulti-RegionalLopez-Camelo JS, et al. [75]July 2005–December 20076.9(5.2, 8.6)14.2(11.8, 16.6)3.2(2.1, 4.4)24.3(21.2, 27.5)
CanadaHighNationalICBDSR 2011 Report [38]2005–20091.0(0.9, 1.2)3.0(2.7, 3.2)0.7(0.6, 0.8)4.6(4.3, 5.0)
ChileHighBio Bio, Los Lagos, Los Rios, Maule, Santiago Metropolitan, O'Higgins, Tarapaca, and Valparaiso RegionsNazer J and Cifuentes L [77]2001–20103.7(3.0, 4.4)4.5(3.7, 5.3)1.7(1.2, 2.1)9.6(8.5, 10.7)
ChileHighMulti-RegionalLopez-Camelo JS, et al.[75]2001–20073.7(2.9, 4.4)4.6(3.8, 5.5)1.8(1.3, 2.3)10.1(8.8, 11.3)
ColombiaUpper-middleCaliPachajoa H, et al.[78]March 2004–October 20086.4(3.9, 9.7)7.3(4.7, 10.8)3.0(1.5, 5.6)16.7(12.3, 21.1)
ColombiaUpper-middleBogota, Ubate, and ManizalesZarante I, et al.[79]April 2001–January 200811.0(8.2, 13.8)
ColombiaUpper-middleBogotaICBDSR 2011 Report [38]20091.6(0.5, 3.8)2.0(0.7, 4.3)0.0(0.0, 1.2)3.6(1.8, 6.5)
ColombiaUpper-middleBaraya, Garzon, Neiva, and PalermoOstos H, et al.[80]19989.6(3.9, 19.8)9.6(3.9, 19.8)1.4(0.0, 7.7)20.6(11.5, 34.0)
Costa RicaUpper-middleNationalde la Paz Barboza-Arguello M, et al.[81]2003–20124.8(4.3, 5.3)
CubaUpper-middleNationalICBDSR 2011 Report [38]2005–20093.8(3.3, 4.3)4.4(3.9, 5.0)1.7(1.4, 2.1)10.0(9.2, 10.8)
EcuadorUpper-middleMulti-RegionalGonzalez-Andrade F and Lopez-Pulles R [82]2001–20070.3(0.3, 0.4)2.5(2.3, 2.7)0.5(0.4, 0.6)3.3(3.1, 3.5)
GuatemalaLower-middleNationalAcevedo CR, et al.[83]2001–20032.3(1.7, 2.9)22.7(20.8, 24.6)3.0(2.3, 3.7)27.9(25.8, 30.0)
HondurasLower-middleTegucigalpaHernandez R and Alvarenga R [84]July 1998–September 200011.9(8.2, 15.5)
MexicoUpper-middleMonterrey, Nuevo LeonHernandez-Herrera RJ, et al.[85]1995–19996.5(5.1, 7.9)8.2(6.6, 9.7)1.3(0.8, 2.1)16.0(13.9, 18.2)
MexicoUpper-middleGuadalajaraAlfaro N, et al.[86]1988–19999.5(8.0, 10.9)10.3(8.8, 11.8)19.7(17.6, 21.8)
MexicoUpper-middleNationalNavarrete Hernandez E, et al.[87]2009–20102.1(1.9, 2.2)1.2(1.1, 1.3)3.3(3.1, 3.5)
MexicoUpper-middleNationalICBDSR 2011 Report [38]2005–20094.6(3.3, 5.9)5.8(4.3, 7.2)1.6(0.9, 2.5)11.9(9.8, 14.1)
PeruUpper-middleLimaSanabria Rojas HA, et al.[88]2006–20101.9(1.1, 3.1)6.1[a](4.5, 7.8)0.1(0, 0.6)8.2[a](6.3, 10.0)
UruguayUpper-middleMontevideoCastilla EE, et al.[89]1999–200117.5(11.9, 23.1)
United StatesHighNationalCanfield MA, et al.[90]1999–20071.3(1.2, 1.4)3.2(3.1, 3.3)0.8(0.7, 0.8)5.3(5.1, 5.4)
VenezuelaUpper-middleMaracaibo, Coro, and Ciudad BolivarCastilla EE, et al.[89]2000–200114.9(11.0, 18.8)
SOUTH-EAST ASIA
BangladeshLowDhakaDey AC, et al.[91]August 2006–July 200713.8(9.2, 20.0)
IndiaLower-middleKolkataSarkar S, et al.[92]September 2011–August 20121.6(0.2, 5.6)14.0(8.3, 22.1)2.3(0.5, 6.8)17.8(11.3, 26.8)
IndiaLower-middleDelhiSood M, et al.[93]January 1988–August 199039.0(26.3, 51.8)26.0(16.7, 38.7)1.1(0.0, 6.0)66.2(49.7, 82.8)
IndiaLower-middleLucknowSharma AK, et al.[94]1982–199119.2(16.8, 21.6)19.6[e](17.2, 22.0)38.8[d](35.4, 42.2)
IndiaLower-middlePondicherryMahadevan B and Bhat BV [95]July 1998–June 200418.0(14.5, 21.6)31.0(26.3, 35.7)7.0(4.8, 9.2)55.5[a](49.3, 61.8)
IndiaLower-middleDuragpurDuttachoudhury A and Pal SK [96]January 1991 -December 19935.5(1.5, 14.1)5.5(1.5, 14.1)11.0(4.8, 21.8)
IndiaLower-middleErodePonne S and Lakshmi UK [97]2000–200410.7(6.6, 12.7)14.7(12.3, 17.2)1.9(1.1, 2.8)27.4(24.1, 30.7)
IndiaLower-middleHimachal Pradesh ShimlaGrover N [98]January 1991–December 199520.8(12.9, 31.8)16.8(9.8, 27.0)6.9(2.8, 14.3)44.6(31.6, 57.5)
IndiaLower-middleMulti-RegionalICBDSR 2011 Report [38]2005–200912.3(11.4, 13.1)11.0(10.2, 11.8)3.6(3.1, 4.0)26.8(25.6, 28.1)
IndiaLower-middleSevagram, WardhaTaksande A, et al.[99]January 2005–July 20075.3(1.7, 12.4)2.1(0.3, 7.7)7.5(3.0, 15.4)
NepalLowThapathaliMalla BK [100]20045.3(2.4, 10.1)4.7(2.0, 9.3)1.8(0.4, 5.2)11.8(7.2, 18.2)
ThailandUpper-middleSongkhla, Phatthalung, and Trang ProvincesJaruratanasirikul S, et al.[101]January 2001–December 20120.8(0.4, 1.4)0.7(0.4, 1.3)0.3(0.1, 0.8)1.9(1.3, 2.7)
ThailandUpper-middleChiang MaiKitisomprayoonkul N and Tongsong T [102]June 1989–May 20005.6(3.9, 7.4)0.6(0.2, 1.5)0.4(0.1, 1.3)6.6(4.7, 8.6)
ThailandUpper-middleBangkokWasant P and Sathienkijkanchai A [103]1990–19992.6(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
AustraliaHighSouth AustraliaFlood L, et al.[104]201019.5(13.4, 25.6)
AustraliaHighVictoria, West Australia, South Australia, New South Wales, Queensland StatesMacaldowie A and Hilder L [105]2006–20088.8(8.2, 9.4)
ChinaUpper-middleHainan ProvinceFan L, et al.[106]20105.8(3.9, 7.7)
ChinaUpper-middleShenzhen CityYang M, et al.[107]2003–20095.7(4.6, 6.8)
ChinaUpper-middleNationalLi X, et al.[108]2006–20085.9(5.6, 6.2)6.0(5.7, 6.3)2.2(2.0, 2.3)14.0(13.4, 14.5)
Northern China6.8(6.4, 7.3)9.2(8.6, 9.8)2.7(2.4, 3.0)18.7(17.9, 19.5)
Southern China5.0(4.6, 5.4)3.1(2.8, 3.4)1.7(1.5, 1.9)9.7(9.1, 10.3)
ChinaUpper-middleInner MongoliaZhang X, et al.[109]2005–20086.9(4.8, 9.0)10.6(8.1, 13.2)2.7(1.4, 4.0)20.3[f](16.8, 23.8)
ChinaUpper-middleNationalDai L, et al. [110]20096.5(6.1, 6.9)
ChinaUpper-middleZhejiang ProvinceZhang XH, et al.[111]2007–20096.3(5.7, 7.0)3.6(3.1, 4.1)1.4(1.1, 1.7)11.3(10.4, 12.2)
ChinaUpper-middleLuliang Prefecture, Shanxi ProvinceChen G, et al.[112]2004–200582.6(60.5, 104.7)38.9(25.2, 57.5)26.5(15.4, 42.4)199.4[d](165.2, 233.6)
ChinaUpper-middleBeijingLi Y, et al.[113]January 2003–March 20090.0(0.0, 0.6)0.3(0.0, 1.2)0.3(0.0, 1.2)
ChinaUpper-middleGuizhou ProvinceLiu J, et al. [114]Januray 1996–December 20044.2(2.9, 5.5)5.9(4.4, 7.4)0.7(0.3, 1.4)12.2[d](10.0, 14.4)
ChinaUpper-middleGansu ProvinceCheng N, et al.[115]January 2001–January 200266.5(46.9, 86.1)
ChinaHighTaiwanChen BY, et al.[116]20021.1(0.7, 1.6)1.1(0.7, 1.6)0.4(0.2, 0.7)2.5(1.9, 3.1)
JapanHighOsaka CityImaizumi Y, et al.[117]1981–19907.1(4.2, 11.4)1.3(0.3, 3.7)8.4(5.1, 12.9)
JapanHighIshikawa PrefectureSeto T, et al.[118]1981–20000.8(0.2, 1.3)0.9(0.3, 1.5)1.0(0.3, 1.6)2.6(1.7, 3.9)
JapanHighNationalICBDSR 2011 Report [38]2005–20090.9(0.6, 1.2)5.2(4.5, 5.9)0.8(0.5, 1.1)6.9(6.1, 7.7)
South KoreaHighNationalKim MA, et al.[119]2005–20060.2(0.1, 0.3)2.6(2.2, 2.9)0.3(0.2, 0.4)3.1(2.7, 3.5)
MalaysiaUpper-middleNationalBoo NY, et al.[120]20092.1(1.5, 2.6)1.6(1.1, 2.1)0.8(0.5, 1.2)5.4(4.5, 6.2)
New ZealandHighNationalICBDSR 2011 Report [38]2005–20090.4(0.2, 0.6)2.1(1.6, 2.6)0.5(0.3, 0.8)3.0(2.4, 3.6)
Papua New GuineaLower-middlePort MoresbyDryden R [121]1985–19863.0(0.6, 8.8)4.0(1.1, 10.2)7.0(2.6, 14.4)
SingaporeHighNationalShi LM, et al.[122]1994–19980.5[b](0.3, 0.9)0.7(0.4, 1.1)1.2[b](0.8, 1.8)
VietnamLower-middleBinh Thuan ProvinceHoang T, et al.[123]20103.6(1.2, 8.4)0.0(0.0, 2.6)0.7(0.0, 4.0)4.3(1.6, 9.4)
UNCLASSIFIED
PalestineEast Jerusalem and Southern West BankDudin A [124]1986–199354.9[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].

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 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.

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].

Bars Indicate the Median Prevalence for Each Condition.

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.

Bars Indicate the Median Percent for Each Condition.

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

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).

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.

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

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 [48-52].
Fig 6

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

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 Neural Tube Defects Prevalence Estimates (Location, Number of Hospitals).

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).

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.

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

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).

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.

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

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).

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.

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

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).

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.

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

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.

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

Data Source: Surveillance/Registry Coverage by Geographic Level.

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 13

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

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 [127-129]. 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].

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  97 in total

1.  [Frequencies of congenital malformations: assessment and prognosis of 52,744 births in three cities of Colombia].

Authors:  Ignacio Zarante; Liliana Franco; Catalina López; Nicolás Fernández
Journal:  Biomedica       Date:  2010 Jan-Mar       Impact factor: 0.935

2.  Neural tube defects in the middle belt of Nigeria.

Authors:  K I Airede
Journal:  J Trop Pediatr       Date:  1992-02       Impact factor: 1.165

3.  A decreasing rate of neural tube defects following the recommendations for periconceptional folic acid supplementation.

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Journal:  Acta Paediatr       Date:  2005-11       Impact factor: 2.299

4.  Incidence, types, geographical distribution, and risk factors of congenital anomalies in Al-Ramadi Maternity and Children's Teaching Hospital, Western Iraq.

Authors:  Zaid R Al-Ani; Shaker A Al-Haj; Muhammad M Al-Ani; Khamees M Al-Dulaimy; Ayad Kh Al-Maraie; Belal Kh Al-Ubaidi
Journal:  Saudi Med J       Date:  2012-09       Impact factor: 1.484

5.  Neural tube defects: a different pattern in northern Thai population.

Authors:  N Kitisomprayoonkul; T Tongsong
Journal:  J Med Assoc Thai       Date:  2001-04

6.  Effect of folic acid fortification on the incidence of neural tube defects.

Authors:  Zouhair O Amarin; Ahmed Z Obeidat
Journal:  Paediatr Perinat Epidemiol       Date:  2010-07-01       Impact factor: 3.980

7.  Associated malformations among infants with neural tube defects.

Authors:  Claude Stoll; Beatrice Dott; Yves Alembik; Marie-Paule Roth
Journal:  Am J Med Genet A       Date:  2011-02-18       Impact factor: 2.802

8.  Prevalence of neural tube defects in economically and socially deprived area of China.

Authors:  Jie Liu; Guo Z Yang; Jin L Zhou; Shi P Cao; David H W Chau; Hsiang-Fu Kung; Marie C Lin
Journal:  Childs Nerv Syst       Date:  2007-04-21       Impact factor: 1.475

9.  Neural tube defects in Switzerland from 2001 to 2007: are periconceptual folic acid recommendations being followed?

Authors:  Andrea Poretti; Tanja Anheier; Roland Zimmermann; Eugen Boltshauser
Journal:  Swiss Med Wkly       Date:  2008-10-18       Impact factor: 2.193

10.  Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies.

Authors:  Lifeng Yan; Lin Zhao; Yan Long; Peng Zou; Guixiang Ji; Aihua Gu; Peng Zhao
Journal:  PLoS One       Date:  2012-10-03       Impact factor: 3.240

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  90 in total

1.  Folate Deficiency Is Prevalent in Women of Childbearing Age in Belize and Is Negatively Affected by Coexisting Vitamin B-12 Deficiency: Belize National Micronutrient Survey 2011.

Authors:  Jorge Rosenthal; Natalia Largaespada; Lynn B Bailey; Michael Cannon; C J Alverson; Dayrin Ortiz; Gail Pa Kauwell; Joe Sniezek; Ramon Figueroa; Robyn Daly; Peter Allen
Journal:  J Nutr       Date:  2017-04-12       Impact factor: 4.798

2.  Fortifying food with folic acid to prevent neural tube defects: are we now where we ought to be?

Authors:  Anne M Molloy; James L Mills
Journal:  Am J Clin Nutr       Date:  2018-06-01       Impact factor: 7.045

3.  Perinatal mortality associated with congenital defects of the central nervous system in Colombia, 2005-2014.

Authors:  M Sierra; J Rumbo; A Salazar; K Sarmiento; F Suarez; I Zarante
Journal:  J Community Genet       Date:  2019-03-29

4.  The Effect of Religious Belief on the Attitudes of Pregnant's Toward the Fetal Health.

Authors:  Emre Demir; Engin Yıldırım
Journal:  J Relig Health       Date:  2019-12

5.  Folate of pregnant women after a nationwide folic acid supplementation in China.

Authors:  Xuejuan Zhang; Jufen Liu; Yongsheng Jin; Shuang Yang; Zhijiao Song; Lei Jin; Linlin Wang; Aiguo Ren
Journal:  Matern Child Nutr       Date:  2019-05-23       Impact factor: 3.092

Review 6.  Finding the genetic mechanisms of folate deficiency and neural tube defects-Leaving no stone unturned.

Authors:  Kit Sing Au; Tina O Findley; Hope Northrup
Journal:  Am J Med Genet A       Date:  2017-09-25       Impact factor: 2.802

7.  Formate rescues neural tube defects caused by mutations in Slc25a32.

Authors:  Jimi Kim; Yunping Lei; Jin Guo; Sung-Eun Kim; Bogdan J Wlodarczyk; Robert M Cabrera; Ying Linda Lin; Torbjorn K Nilsson; Ting Zhang; Aiguo Ren; Linlin Wang; Zhengwei Yuan; Yu-Fang Zheng; Hong-Yan Wang; Richard H Finnell
Journal:  Proc Natl Acad Sci U S A       Date:  2018-04-16       Impact factor: 11.205

8.  Posterior Fontanelle Encephalomeningocele in a Neonate: A Case Report.

Authors:  Abdurrahman Raeiq
Journal:  Cureus       Date:  2018-03-13

9.  Snx3 is important for mammalian neural tube closure via its role in canonical and non-canonical WNT signaling.

Authors:  Heather Mary Brown; Stephen A Murray; Hope Northrup; Kit Sing Au; Lee A Niswander
Journal:  Development       Date:  2020-11-19       Impact factor: 6.868

10.  Oxidative stress response associates with the teratogenic effects of benzyl butyl phthalate (BBP).

Authors:  Ge Song; Rui Wang; Yi Cui; Chan Juan Hao; Hong-Fei Xia; Xu Ma
Journal:  Toxicol Res (Camb)       Date:  2020-05-08       Impact factor: 3.524

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