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Copyright © 2005, BMJ Publishing Group Ltd. International retrospective cohort study of neural tube defects in relation to folic acid recommendations: are the recommendations working? 1 National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA 2 International Centre on Birth Defects, Rome 00195, Italy 3 Institut Européen des Génomutations, 69005 Lyon, France 4 Section for Epidemiology and Medical Statistics, University of Bergen, NO-5018 Bergen, Norway 5 Medical Birth Registry, Norwegian Institute of Public Health, NO-5018 Bergen 6 Office for National Statistics, London SW1V 2QQ 7 Department of Neonatalogy and Preventive Paediatrics, University of Bologna, 40138 Bologna, Italy 8 Northern Netherlands Registry of Birth Defects, Department of Medical Genetics, University of Groningen, 9713 AW Groningen, Netherlands 9 Portuguese Birth Defects Registry (CERAC), National Institute of Health, 1649-016 Lisbon, Portugal 10 Dublin EUROCAT Registry of Congenital Anomalies, Department of Public Health, Eastern Regional Health Authority, Dublin 8, Republic of Ireland 11 Department of Neonatology, Rabin Medical Center, Petah Tikva 49100, Israel 12 Finnish Register of Congenital Malformations, National Research and Development Centre for Welfare and Health (STAKES), FIN-00531 Helsinki, Finland 13 Department of Genetics, AO “G Rummo,” Benevento, Italy 14 Hungarian Congenital Abnormality Registry, Department of Human Genetics and Teratology, National Center for Epidemiology, H-1966 Budapest, Hungary 15 Strasbourg Birth Defects Registry, Faculty of Medicine, University of Strasbourg, 67085 Strasbourg Cedex, France 16 University of Leeds, Leeds 17 Paris Birth Defects Registry, INSERM U149, 94807 Villejuif Cedex, France Correspondence to: L D Botto icbd/at/icbd.org Accepted December 9, 2004. This article has been cited by other articles in PMC.Abstract Objectives To evaluate the effectiveness of policies and recommendations on folic acid aimed at reducing the occurrence of neural tube defects. Design Retrospective cohort study of births monitored by birth defect registries. Setting 13 birth defects registries monitoring rates of neural tube defects from 1988 to 1998 in Norway, Finland, Northern Netherlands, England and Wales, Ireland, France (Paris, Strasbourg, and Central East), Hungary, Italy (Emilia Romagna and Campania), Portugal, and Israel. Cases of neural tube defects were ascertained among liveborn infants, stillbirths, and pregnancy terminations (where legal). Policies and recommendations were ascertained by interview and literature review. Main outcome measures Incidences and trends in rates of neural tube defects before and after 1992 (the year of the first recommendations) and before and after the year of local recommendations (when applicable). Results The issuing of recommendations on folic acid was followed by no detectable improvement in the trends of incidence of neural tube defects. Conclusions Recommendations alone did not seem to influence trends in neural tube defects up to six years after the confirmation of the effectiveness of folic acid in clinical trials. New cases of neural tube defects preventable by folic acid continue to accumulate. A reasonable strategy would be to quickly integrate food fortification with fuller implementation of recommendations on supplements. Introduction Improving children's survival and health worldwide requires effective primary prevention of birth defects. In many developed countries, birth defects already account for one in every four infant deaths and for an unknown number of fetal deaths and pregnancy terminations.1,2 However, because of their large birth population and the few resources available for treatment and rehabilitation, developing countries bear most of the global burden of birth defects.1 Primary prevention of certain serious birth defects is now feasible globally. The groundbreaking studies of Smithells and colleagues,3-5 confirmed by many other studies and randomised clinical trials by the early 1990s,6-9 showed that supplements containing folic acid, a B vitamin, when consumed from before conception, can reduce spina bifida and other neural tube defects by an estimated 80% or more. Neural tube defects, which also include anencephaly, are severe and often lethal conditions that annually affect at least 300 000 newborns worldwide.1,7,10 Accumulating data indicate additional benefits of folic acid on other major birth defects.11 Because folic acid is inexpensive, safe, and easy to use, many professional organisations and some governmental agencies promote the use of folic acid supplements to prevent neural tube defects. The format of such recommendations varies, but they typically include statements that women should eat a healthy diet and take folic acid supplements when planning a pregnancy or throughout childbearing age. In a few countries, including the United States, Canada, Chile, and South Africa, recommendations to consume folic acid are integrated with a policy of wide-spread fortification of flour to ensure that the entire population receives at least a small additional amount of folic acid regardless of access to supplements. This population-wide approach is effective,12-14 but it is used in only a few countries. A crucial question is how effective are recommendations alone, in the absence of fortification. We examined this question by evaluating rates of neural tube defects and their temporal relation with recommendations on folic acid. Methods The study included selected registries from the International Clearinghouse for Birth Defects Monitoring Systems. Major criteria for inclusion were a structure for population based ascertainment; relatively large size; and ability to provide detailed case information for central clinical review, ascertain affected pregnancy terminations (where such a procedure was legal), and conduct an assessment of local folic acid policy development. The nature of the funding sources, primarily from Europe, led to the preferential inclusion of European registries. Although initially included, US registries were later excluded because of the introduction of fortification of flour. We gathered information on folic acid recommendations from interviews, publications listed on Medline, reports of workshops and committees, and documents issued by governmental agencies and professional bodies. Thirteen registries provided listings of cases of anencephaly or spina bifida among liveborn infants, stillbirths, and pregnancy terminations that occurred between 1988 and 1998. Case information also included birth outcome, birth date, gestational age, and associated malformations. Registries also provided appropriate denominator information. To adjust for temporal and geographical variations in the timing of pregnancy terminations, we assigned affected pregnancy terminations to the calendar year in which they would have been delivered had they reached the mean gestational age of liveborn cases in the database (adjusted by registry and birth year). We use the term “incidence” for the reported rates, although the true population at risk for neural tube defects (all conceptuses) cannot be ascertained. We plotted incidences by year, programme, and type of neural tube defect (anencephaly and spina bifida). We used Poisson regression to assess trends. From the Poisson regression, we derived for each programme an incidence rate ratio, which estimates the average relative change in rate per year. For example, an incidence rate ratio of 1.00 indicates no change (a flat regression line), whereas a ratio of 0.80 indicates a 20% average decrease and a ratio of 1.20 indicates a 20% average increase from one year to the next. We calculated incidence rate ratios for the entire study period as well as for before and after 1992 and before and after the year of introduction of national recommendations (where these had been issued). We chose 1992 because of the timing of the publication of the randomised trials (1991 and 1992) and of the recommendations in the United States and the United Kingdom (in 1992), which were internationally known and available to all interested parties. We used the incidence by year and by programme, derived from Poisson regression, diminished by the appropriate prevented fraction (30% to 90%), to estimate the number of cases that might have been prevented in the study area since 1992 at different levels of folic acid effectiveness. Results The study included 8636 cases of anencephaly or spina bifida among over 13 million births in 13 areas in Europe and Israel (table 1). Relative to other study areas, rates of neural tube defects tended to be higher in Ireland, Northern Netherlands, and France (Paris) (fig 1
Folic acid policies during the study period varied from no recommendations (Italy and Israel) or dietary recommendations only (Norway until 1998) to dietary recommendations plus use of supplements among selected women (Finland) or use of supplements for women planning pregnancy or all women of childbearing age (table 2). The timing of the recommendations also varied, with some programmes—such as those in the United Kingdom and Ireland—issuing recommendations as early as 1992.
In most areas rates were stable, as indicated by incidence rate ratios statistically undistinguishable from one (table 3). Four areas showed an overall decreasing trend (table 3). Trends after 1992 were similar to trends before 1992 (table 4). In Italy (Campania), trends seemed to vary across the two periods, but these variations were within statistical fluctuations. In Hungary, reported rates seemed to decrease then increase towards the end of the study period. A retrospective assessment identified underascertainment of affected pregnancy terminations in the mid-1990s due to organisational changes in the reporting system in Hungary, and for this reason we excluded pregnancy terminations from Hungarian data in the tables 4 and 5 and figures figures11
We also saw no material change in trends after the issuing of local recommendations (table 5). Findings were similar for anencephaly and spina bifida separately and combined. The number of cases that might have been prevented in the study area beginning in 1993 ranged from 1287 (assuming 30% effectiveness), through 2574 (for 60% effectiveness), to 3861 (for 90% effectiveness) (fig 2 Discussion In this study covering more than 13 million births, rates of neural tube defects showed no detectable change associated with recommendations to consume more folic acid. Either rates were unchanged or the decline was similar to that observed during the period before the recommendations. From these data, we estimate that thousands of pregnancies that would otherwise have been healthy were affected by neural tube defects in the study area alone since 1992 (fig 2 Limitations and strengths The study has some potential limitations. Firstly, case ascertainment may have varied by registry and thus probably contributed to the geographical variation in reported rates (table 1). Incomplete ascertainment does not necessarily invalidate monitoring if it remains constant over time. Constant ascertainment is difficult to prove, and variations may have occurred, particularly among pregnancy terminations. In Hungary (fig 1 A second limitation is that the use of ecological data may have led to real effects going undetected. Rates may have decreased locally, for example, in areas in the Netherlands and Ireland that conducted extensive educational campaigns,16,17 but we may have been unable to observe them, because of the nature of the data and limited sample size. A third limitation is the study's limited geographical scope. The focus on European areas was related partly to the funding source and partly to the availability of data from relatively large and established registries with information on pregnancy terminations. A more comprehensive view would be desirable and useful. However, the study findings in Europe, where birth defects are a major contributor to infant death, are likely to be relevant to a more global discussion on missed opportunities for prevention of neural tube defects. Finally, we had incomplete information on the extent of implementation of recommendations. Such information is crucial if we are to understand why recommendations did not reduce the incidence of disease. The study also had several strengths. We included areas with a range of reported rates and recommendations, from none at all (Italy) to early adoption of recommendations in association with educational campaigns (for example, Ireland). The registries used multiple sources of ascertainment, including pregnancy terminations. Finally, the findings were not confounded by fortification of flour. Possible explanations and implications Why did recommendations have no detectable effect on rates, despite the proved effectiveness of folic acid? The most likely possibility is that recommendations were not implemented to the point of inducing a sustained change in behaviour in a sufficiently large proportion of women to cause measurable effects. Folic acid use increased in the Netherlands and the United Kingdom in conjunction with government sponsored education campaigns,17,18 but the long term persistence and effects are unknown. Otherwise, folic acid use in Europe is generally very low—approximately 10% in Norway in 1998,19,20 and 6% in Italy in 2002 (Botto and Bianchi, unpublished data).
Whereas any improvement in primary prevention is desirable and should be promoted, a detectable change in the population requires a major shift in the proportion of women consuming adequate amounts of folic acid. It is unclear how successful recommendations alone will be in achieving this goal, given the influence of cultural, social, and economic factors such as the acceptability, availability, and cost of daily supplements. Intensive educational efforts and a very high proportion of planned pregnancies seem to have been crucial factors in the high effectiveness of a public health campaign to promote use of folic acid supplements in areas of China.7 In general, use of supplements tends to follow economic and educational lines,17-19 so targeting the entire population through recommendations on supplementation alone may not be practical. In this context, fortification of flour represents an additional opportunity to deliver some folic acid to nearly the entire population, across social and economic barriers. Where dietary and food processing conditions are favourable, fortification can be effective quickly and at low cost. In countries that have fortified flour, blood folate concentrations have risen quickly,14,21,22 and although the reductions in incidence were not as large as that achievable through supplementation, such reduction occurred soon after fortification was implemented.12-14 This element of timeliness is crucial. As figure 2 Notes The study was conducted under the auspices of the French National Institute of Health and Medical Research (INSERM). A Rosano and T Dukic provided technical assistance in the initial phases of the study. The lateRichard (Dick) Smithells was one the leaders of this study, from its conception through planning and initial report writing. We were immensely privileged to work with Professor Smithells, who sadly could not see this study to completion. Contributors: LDB, ER-G, SEV, PM, JDE, and JG developed the protocol and coordinated the study. JG secured the initial funding, and JG and LDB directed the study. LDB, JG, and SEV developed the analysis, and AL and LDB carried it out. LDB and JG wrote the original draft, worked to secure funding, and directed the study. BB, CdV GC, HdW, MF, LMI, BMcD, PM, AR, GS, CS, JM, and CS generated and provided the data, participated in study development, and contributed to writing the report. LDB is the guarantor. Funding: European Community (BIOMED Concerted Action PL 96 393 63), US Centers for Disease Control and Prevention (U50/CCU207141). Competing interests: None declared. Ethical approval: Participating registries operate under approval of local institutional review boards (IRB), and the joint analysis was done on anonymous data from monitoring systems exempt from IRB approval. References 1. Shibuya K, Murray CJL. Congenital anomalies. In: Murray CJL, Lopez AD, eds. Health dimensions of sex and reproduction. Boston: Harvard University Press, 1998: 455-512. 2. Centers for Disease Control and Prevention. Trends in infant mortality attributable to birth defects—United States, 1980-1995. MMWR Morb Mortal Wkly Rep
1998;47: 773-8. [PubMed] 3. Smithells RW, Sheppard S, Schorah CJ. Vitamin deficiencies and neural tube defects. Arch Dis Child
1976;51: 944-50. [PubMed] 4. Smithells RW, Sheppard S, Schorah CJ, Seller MJ, Nevin NC, Harris R, et al. Possible prevention of neural-tube defects by periconceptional vitamin supplementation. Lancet
1980;i: 339-40. 5. Smithells RW, Nevin NC, Seller MJ, Sheppard S, Harris R, Read AP, et al. Further experience of vitamin supplementation for prevention of neural tube defect recurrences. Lancet
1983;i: 1027-31. 6. Botto LD, Moore CA, Khoury MJ, Erickson JD. Neural-tube defects. N Engl J Med
1999;341: 1509-19. [PubMed] 7. Berry RJ, Li Z, Erickson JD, Li S, Moore CA, Wang H, et al. Prevention of neural-tube defects with folic acid in China: China-U.S. Collaborative Project for Neural Tube Defect Prevention. N Engl J Med
1999;341: 1485-90. [PubMed] 8. Czeizel AE, Dudas I. Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med
1992;327: 1832-5. [PubMed] 9. MRC Vitamin Study Research Group. Prevention of neural tube defects: results of the Medical Research Council vitamin study. Lancet
1991;338: 131-7. [PubMed] 10. Oakley GP. Delaying folic acid fortification of flour. BMJ
2002;324: 1348-9. [PubMed] 11. Botto LD, Olney RS, Erickson JD. Vitamin supplements and the risk for congenital anomalies other than neural tube defects. Am J Med Genet
2004;125C: 12-21. 12. Castilla EE, Orioli IM, Lopez-Camelo JS, Dutra Mda G, Nazer-Herrera J. Preliminary data on changes in neural tube defect prevalence rates after folic acid fortification in South America. Am J Med Genet
2003;123A: 123-8. 13. Honein MA, Paulozzi LJ, Mathews TJ, Erickson JD, Wong LY. Impact of folic acid fortification of the US food supply on the occurrence of neural tube defects. JAMA
2001;285: 2981-6. [PubMed] 14. Ray JG, Meier C, Vermeulen MJ, Boss S, Wyatt PR, Cole DE. Association of neural tube defects and folic acid food fortification in Canada. Lancet
2002;360: 2047-8. [PubMed] 15. Rosano A, Botto LD, Botting B, Mastroiacovo P. Infant mortality and congenital anomalies from 1950 to 1994: an international perspective [see comments]. J Epidemiol Community Health
2000;54: 660-6. [PubMed] 16. Oleary M, Donnell RM, Johnson H. Folic acid and prevention of neural tube defects in 2000 improved awareness—low peri-conceptional uptake. Ir Med J
2001;94: 180-1. [PubMed] 17. De Walle HE, Cornel MC, de Jong-van den Berg LT. Three years after the Dutch folic acid campaign: growing socioeconomic differences. Prev Med
2002;35: 65-9. [PubMed] 18. Landon J, Thorpe L. Changing preconceptions: the HEA folic acid campaign 1995-1998. Vol 1 London: Health Education Authority, 1998: 61-2. 19. Vollset SE, Lande B. Knowledge and attitudes of folate, and use of dietary supplements among women of reproductive age in Norway 1998. Acta Obstet Gynecol Scand
2000;79: 513-9. [PubMed] 20. Daltveit AK, Vollset SE, Lande B, Oien H. Changes in knowledge and attitudes of folate, and use of dietary supplements among women of reproductive age in Norway 1998-2000. Scand J Public Health
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2002;51: 808-10. [PubMed] 22. Hirsch S, de la Maza P, Barrera G, Gattas V, Petermann M, Bunout D. The Chilean flour folic acid fortification program reduces serum homocysteine levels and masks vitamin B-12 deficiency in elderly people. J Nutr
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[MMWR Morb Mortal Wkly Rep. 1998]Arch Dis Child. 1976 Dec; 51(12):944-50.
[Arch Dis Child. 1976]N Engl J Med. 1999 Nov 11; 341(20):1509-19.
[N Engl J Med. 1999]Lancet. 1991 Jul 20; 338(8760):131-7.
[Lancet. 1991]N Engl J Med. 1999 Nov 11; 341(20):1485-90.
[N Engl J Med. 1999]BMJ. 2002 Jun 8; 324(7350):1348-9.
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[Lancet. 2002]J Epidemiol Community Health. 2000 Sep; 54(9):660-6.
[J Epidemiol Community Health. 2000]Ir Med J. 2001 Jun; 94(6):180-1.
[Ir Med J. 2001]Prev Med. 2002 Jul; 35(1):65-9.
[Prev Med. 2002]Prev Med. 2002 Jul; 35(1):65-9.
[Prev Med. 2002]Acta Obstet Gynecol Scand. 2000 Jun; 79(6):513-9.
[Acta Obstet Gynecol Scand. 2000]Scand J Public Health. 2004; 32(4):264-71.
[Scand J Public Health. 2004]N Engl J Med. 1999 Nov 11; 341(20):1485-90.
[N Engl J Med. 1999]Prev Med. 2002 Jul; 35(1):65-9.
[Prev Med. 2002]Acta Obstet Gynecol Scand. 2000 Jun; 79(6):513-9.
[Acta Obstet Gynecol Scand. 2000]Lancet. 2002 Dec 21-28; 360(9350):2047-8.
[Lancet. 2002]MMWR Morb Mortal Wkly Rep. 2002 Sep 13; 51(36):808-10.
[MMWR Morb Mortal Wkly Rep. 2002]J Nutr. 2002 Feb; 132(2):289-91.
[J Nutr. 2002]