Oncotarget

Research Papers:

The recurrence risk of neural tube defects (NTDs) in a population with high prevalence of NTDs in northern China

PDF |  HTML  |  Supplementary Files  |  How to cite

Oncotarget. 2017; 8:72577-72583. https://doi.org/10.18632/oncotarget.19890

Metrics: PDF 1459 views  |   HTML 2674 views  |   ?  

Jufen Liu, Zhiwen Li _, Nicholas D.E. Greene, Hongtian Li and Aiguo Ren

Abstract

Jufen Liu1,2, Zhiwen Li1,2, Nicholas D.E. Greene3, Hongtian Li1,2 and Aiguo Ren1,2

1Institute of Reproductive and Child Health/Key Laboratory of Reproductive Health, National Health and Family Planning Commission of the People’s Republic of China, Peking University, Beijing, P. R. China

2Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, P. R. China

3UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom

Correspondence to:

Zhiwen Li, email: [email protected]

Keywords: recurrence, neural tube defects, folic acid, supplementation, China

Abbreviations: NTDs: neural tube defects, FA: folic acid

Received: May 24, 2017    Accepted: July 13, 2017    Published: August 03, 2017

ABSTRACT

Background: Although a number of studies have reported the recurrence risk of NTDs in developed countries, there is little data on the rate of recurrence of NTDs in northern China, a region of high prevalence of NTDs.

Methods: Based on the population-based birth defects surveillance system of five counties, we identified women who had an NTD affected pregnancy from 2004-2015 and a retrospective survey was conducted. The rate of recurrence of NTDs was calculated by the number of recurrent NTDs divided by the first NTDs. Maternal age, body mass index (BMI), gestational weeks, education, and occupation were collected. Information on folic acid (FA) supplements, time and dosage were also recorded.

Results: Among 851 women who had a previous NTD-affected pregnancy, there were 578 subsequent pregnancies, with 10 recurrent NTDs, a 1.7% recurrence rate. The recurrence rate was 1.5% and 2.6% for those taking FA supplements and without FA supplementation respectively. Women with recurrent NTDs had higher BMI before pregnancy compared to those who had a second pregnancy without NTDs. Among the recurrent NTDs, the majority were spina bifida.

Conclusions: The recurrence rate of NTDs was approximately five times higher than the overall prevalence in the same region of northern China. Risk of recurrence appeared lower among women who took FA supplements. These findings are consistent with the reduction in NTD frequency in the population since introduction of the nationwide FA supplement program. Data on recurrence rates in northern China will inform power calculations for future intervention studies.


INTRODUCTION

Neural tube defects (NTDs), such as anencephaly and spina bifida are common and severe malformations of the developing central nervous system. Women who have had a pregnancy affected by an NTD have an elevated risk of a subsequent NTD-affected pregnancy [1]. Several studies report the recurrence risk of NTDs in developed countries [2-4]. The recurrence rate was 3.0% (95% confidence limits: 2.0-4.3%) in the United States in the late 1970s [5], 2.9% in Belgium [4] and 1.2-1.7% in England [2, 3]. However, these studies have limited sample size, typically less than around one or two hundred [2-4], with only one study including around 1000 cases [6].

The prevalence of NTDs in China is among the highest worldwide [7], but studies reporting prevalence have not categorized the risk of occurrence and recurrence [8-10]. For example, the prevalence of total NTDs was 1.2% in 2004 and 0.79% in 2009, declining to 0.32% in 2014 [10]. Hence, prevalence is approximately 10 times higher than rates in the USA and Europe [11, 12]. Only one study reported an estimate of recurrence risk of NTDs, based on a retrospective survey in the early 1990s. The overall recurrence was 6.9%, with differing rates in low, average and high prevalence areas of 3.7%, 4.5% and 8.3%, respectively [13]. Because the recurrence rate of NTDs was related to the incidence of NTDs in the general population [5, 14], and the prevalence of NTDs has declined dramatically in recent years, the recurrence risk of NTDs may be quite different from two decades ago, in particular since the introduction of a folic acid supplementation programme.

Maternal supplementation with folic acid (FA) in the periconceptional period significantly reduces the risk of NTDs, both occurrent and recurrent [6, 15-17]. A meta-analysis of the randomized trials indicated a 69%-87% reduction with use of FA for the prevention of recurrent NTDs and a 85–100% reduction in observational studies [1]. However, some of those studies were conducted prior to the widespread use of folic acid supplements and fortification of enriched cereal grain products [5], and some compared a specific vitamin supplement, for example, Pregnavite Forte F [2]. The prevention effect of population-based supplementation of folic acid has not been studied in Chinese people.

Using a population-based birth-defect surveillance system and a retrospective survey, the current study aimed to examine the recurrence of NTDs in 5 counties of Shanxi province, China, and to gain information on the impact of the FA supplement program since 2009. The study addressed three main issues, with the major aim being to determine the risk of NTD recurrence in a population with a high prevalence of NTDs. Our second aim was to evaluate, in a population with a first affected pregnancy, the use of FA supplements in a subsequent pregnancy, to determine whether FA supplementation had any protective effects. The third aim was to obtain information on the dietary characteristics of women who suffer recurrent NTDs.

RESULTS

In all, 1547 NTD cases were identified from 2004 to 2015 in the five counties, and 851 cases were followed up in this survey, a follow-up rate of 55%. There were no apparent significant differences between mothers who participated in the follow-up study and cases in which the mother did not participate. There were 578 subsequent pregnancies following 851 first NTDs, with 10 recurrent NTDs, corresponding to an overall recurrence rate of 1.7% (10/578). The recurrence rate was 1.5% (7/456) in those taking FA supplements and 2.6% (3/117) in those who were not taking such supplements ( P=0.434).

There were no significant differences in age, occupation, or education between women with recurrent NTD pregnancies and those with unaffected pregnancies. However, women who suffered a recurrent NTD had a higher BMI before pregnancy than those who did not (P<0.05) (Table 1).

Table 1: Characteristics of the subjects [M (SD) or n (%)]

Characteristics

Women with first NTDs (N=851)

Women with second pregnancy after occurrent NTD (N=578)

Women with recurrent NTDs (N=10)

Women without recurrent NTDs (N=568)

P*

Age

28.0(5.6)

26.5(4.8)

26.4(4.6)

26.5(4.8)

0.955

BMI

23.5(3.3)

23.4(3.2)

27.5(5.2)

23.3(3.2)

<0.001

Gestational weeks

25.3(8.0)

24.7(7.5)

22.1(4.5)

39.2(3.5)

<0.001

Occupation

Farmers

636(74.7)

423(73.2)

8(80.0)

415(73.1)

0.855

Others

205(24.1)

148(25.6)

2(20.0)

146(25.7)

Missing

10(1.2)

7(1.2)

0

7(1.2)

Education

Primary school

104(12.2)

60(10.4)

2(20.0)

58(10.2)

0.754

Junior high school

613(72.0)

423(73.2)

7(70.0)

416(73.2)

Senior high school and above

126(14.8)

92(15.9)

1(10.0)

91(16.0)

Missing

8(0.9)

3(0.5)

0

3(0.5)

* Compared between recurrent NTDs and the second pregnancy without NTDs

The proportion of women who took FA supplements in their second pregnancy was lower among women who suffered recurrent NTDs than those who did not (P<0.05) (Table 2). Among the first NTD pregnancies, 73% of women reported taking FA supplements after they knew they were pregnant which was too late to prevent NTDs. In a recurrent NTD, 30% of women took FA after pregnancy (Table 3). The majority of women in each group took FA at a dose of 0.4 mg per day and only one individual took more than 5 mg per day.

Table 2: Characteristics of NTDs in first and recurrent pregnancy [n(%)]

Characteristics

First NTDs (N=851)

Second pregnancy (N=578)

Recurrent NTDs (N=10)

Second pregnancy without NTDs (N=568)

P*

Types of defects

Anencephaly

379(44.5)

3(0.5)

3(30.0)

Spina bifida

398(46.8)

6(1.0)

6(60.0)

Encephalocele

74(8)

1(0.2)

1(10.0)

Other type

19(3.3)

0

No BD

542(93.8)

Male

383(45.0)

309(53.5)

5(50.0)

304(53.5)

<0.001

Sex

Female

372(43.7)

258(44.6)

3(30.0)

255(44.9)

Bisexual

1(0.1)

0

Unknown

95(11.2)

11(1.9)

2(20.0)

9(1.6)

FA supplements

Yes

233(27.4)

455(78.7)

7(70.0)

449(79.0)

0.012

No

586(68.9)

117(20.2)

3(30.0)

114(20.1)

Missing

32(3.8)

6(1.0)

5(0.9)

FA supplements before pregnancy

Yes

63(7.4)

276(47.8)

3(30.0)

273(48.1)*

*Compared between recurrent NTDs and the second pregnancy without NTDs

Table 3: Description of folic acid supplement for the first and second pregnancy (among those taking folic acid)

Folic acid (FA) supplement

First NTDs (N=233)

Second pregnancy (N=455)

Recurrent NTDs (N=7)

Second pregnancy without NTDs (N=449)

P*

Period of FA supplementation

0.770

 3 months before pregnancy

31(13.3)

218(37.7)

3(43.0)

215(37.9)

 2 months before pregnancy

7(3.0)

27(4.7)

0

27(4.8)

 1 month before pregnancy

25(10.7)

31(5.4)

0

31(5.5)

 After pregnancy

170(73.0)

179(31.0)

4(57.0)

175(30.8)

 Missing

0

123(21.3)

0

120(21.1)

FA supplements dose

0.722

 0.4 mg

331(57.3)

4(57.0)

327(57.6)

 0.8 mg

36(6.2)

1(14.0)

35(6.2)

 1-3 mg

6(1.0)

0

6(1.1)

 ≥4 mg

69(11.9)

1(14.0)

68(12.0)

 Missing

136(23.5)

1(14.0)

132(23.2)

*Compared between recurrent NTDs and the second pregnancy without NTDs

The majority of first NTDs were anencephaly or spina bifida, which accounted for 80% of all NTDs. The types of NTDs affecting successive pregnancies for each mother were not necessarily the same in each case. Three pregnancies affected by anencephaly were followed by spina bifida in the second pregnancy, two spina bifida-affected pregnancies were followed by anencephaly, and one anencephaly was followed by an encephalocele (Table 4). Male and female babies were both represented among recurrent NTDs. In addition to NTDs, a number of other malformations or abnormal post-natal outcomes were also reported among women who had previously suffered an NTD-affected pregnancy (Table 4).

Table 4: Characteristics of two pregnancies with birth defects by types [n(%)]

First pregnancy

Second pregnancy

Frequency

Anencephaly

Spina bifida

3

Anencephaly

Cleft palate

1

Anencephaly

Encephalocele

1

Anencephaly

Miscarriage

1

Anencephaly

Cardiac defect

1

Anencephaly

Embryo arrest

1

Anencephaly

Autism

1

Anencephaly

Others BD, but don’t know the type

2

Spina bifida

Spina bifida

3

Spina bifida

Anencephaly

3

Spina bifida

Cerebral palsy

2

Spina bifida

Embryo arrest

2

Spina bifida

Hypospadias

1

Spina bifida

Others BD, but don’t know the type

5

Encephalocele

Ear malformation

1

The average interval between NTD pregnancies in our sample was 44.5 ± 32.0 months. The shortest interval was 9 months and the longest was 9 years, with 40% of second pregnancies occurring within 2 years of the first pregnancy and 60% occurring after 2 years or more (Table 5). There were no significant differences in reported dietary frequency except for tea consumption (Supplementary Table 1) between women who had a recurrent NTD and those who did not.

Table 5: Interval between two pregnancies with NTDs

Case number

First pregnancy

Second pregnancy

Interval(month)

1

Anencephaly

Encephalocele

46

2

Anencephaly

Spina bifida

108

3

Spina bifida

Spina bifida

19

4

Spina bifida

Spina bifida

42

5

Spina bifida

Spina bifida

9

6

Anencephaly

Spina bifida

18

7

Anencephaly

Spina bifida

71

8

Spina bifida

Anencephaly

31

9

Spina bifida

Anencephaly

79

10

Spina bifida

Anencephaly

22

Mean (SD)

44.5(32.0)

DISCUSSION

We investigated the recurrence rate of NTDs in a region of historically high prevalence of NTDs in China. Among 578 pregnancies following a previous NTD-affected pregnancy, the total recurrence risk was 1.7%. Among recurrent NTDs, the prevalence among women who did not take folic acid supplements was almost double that of those who take folic acid supplements (2.6% vs 1.5%). The prevalence of NTDs in the study area was 0.32% in 2014, which was approximately ten times higher than in the USA [10] and 2.5 times higher than another northern province Liaoning (0.13%) [18] at same time. The rate of recurrent NTDs was 5 times higher than the prevalence of NTDs in the same area of China.

The recurrence rate in our study was similar to that reported in England, 1.2-1.7% in early 1990s [3, 2], and was much lower than the previously reported recurrence risk of NTDs in China in the early 1990s [13]. This difference in recurrence rate occurred in parallel with a reduction in the overall prevalence of NTDs which may be attributable to the nationwide folic acid supplementation program initiated in 2009. The same trend was found in Liaoning [18]. The program provides free folic acid tablets to all women who have a rural registration and who plan to become pregnant [10, 19, 20].

Clinical trials and the outcome of fortification campaigns show that folic acid supplementation can prevent first occurrence of NTDs and recurrent NTDs. Our study suggests that a lower proportion of women with recurrent NTDs took FA supplements than women who did not have a recurrent NTDs. Among women who had a previous affected pregnancy, less than 50% took FA in the period before their next pregnancy, suggesting that health education initiatives should emphasize the optimal period of supplementation as well as dosage of FA supplement that is protective. As formation of the neural tube occurs during weeks 3-4 of pregnancy, it is too late for women to take folic acid after they know they are pregnant. To obtain optimal blood folate levels to prevent NTDs, it recommended to supplement FA in the periconceptional period (28 days before through 28 days after the last menstrual period) [21]. Moreover, to prevent NTD recurrence, a dose of 4-5 mg FA per day is recommended, as compared with 0.4 mg, based on the findings of the MRC Vitamin study in which the risk of recurrent NTDs was reduced by 72% [6].

Although folic acid supplementation may not be able to prevent all NTDs, it is clear that it has a protective effect. NTDs still arise in regions that have mandated FA fortification of enriched cereal grain products. For example, the rate of NTDs in South Carolina, USA, remained at 0.66 NTDs per 1,000 live births and fetal deaths after 20 years of extensive promotion of periconceptional FA use and 14 years of fortification of cereal grain flour [23]. In contrast to the food fortification approach of the USA and other countries, China implemented a public health campaign to provide FA tablets (0.4 mg per day) to women who may become pregnant. Although the tablets are provided free of charge, the compliance is not satisfactory; our previous study showed that the percentage of FA supplementation before the last menstrual period is around 40% [20]. Folic acid fortification of staple foods could be recommended to further prevent NTDs in China [10].

Our study found that the BMI of women who had a second NTD-affected pregnancy was higher than that of women who did not. It is possible that this contributed to NTD risk, as a higher BMI has been found to be an independent risk factor for NTDs [24, 25]. A population-based case-control study revealed that pre-pregnancy maternal overweight/obese women were more likely than average-weight women to have an infant with spina bifida, heart defects and multiple anomalies [25]. A meta-analysis reported that the odds ratio of NTDs in offspring was 1.04 (95% CI 1.027–1.051) for every 1 kg/m2 BMI increase in mothers, and indicated that maternal obesity is an important risk factor for NTDs in offspring [24]. Maternal obesity is a risk factor for adverse pregnancy outcome, suggesting that obesity prevention efforts are needed to increase the number of women who are of healthy weight before pregnancy.

Our study had several strengths. First, it was based on a population-based surveillance system, and the surveillance covered 95.6% of births [7], which ensures quality data. Second, the NTDs were double checked by local doctors and pediatricians from Peking University, which ensures the accuracy of diagnosis. However, several limitations prohibited further analysis. One limitation of the present study was that it may have underestimated the recurrent risk of NTDs because almost half of the participants were not followed up. The second limitation was that it included only five counties, and the results may not be generalizable to the entire province or country. The third limitation was that few risk factors were evaluated, which hindered our ability to explore the risk factors for recurrent NTDs. Future studies should use a larger sample size and collect more information.

In conclusion, the prevalence of recurrent NTDs remains high in the research area, although implementation of the FA supplementation program has been associated with lower overall prevalence of NTDs. Improving the compliance of FA supplementation as a public health campaign could lead to further reduction of the prevalence of NTDs. Some recurrent NTDs arose despite the use of FA supplements, suggesting that further investigations of other NTD risk factors and/or preventive measures are warranted.

MATERIALS AND METHODS

Subjects

The study was based on the population-based birth defects surveillance system of five counties (Pingding, Xiyang, Taigu, Zezhou and Shouyang) in northern China [7, 10].

Followed the model of a public health campaign which was to evaluate the effect periconceptional folic acid supplementation to prevent NTDs [26], the surveillance system covers more than 20,000 births in the above five counties each year. Any infant suspected of having a major structural external birth defect by prenatal diagnosis or at delivery is reported by local health care providers. Information of preliminary diagnosis of birth defects and basic demographic information, including birth date, sex, birth order and a detailed clinical description (including measurements where applicable) of the birth defect(s) were collected and a photograph of affected infants was taken within the first 24 h after delivery. Definitive diagnosis, classification and coding of structural birth defects were conducted by a clinical geneticist from Peking University. These data can be used for descriptive epidemiology of birth defects [26]. Details of the surveillance system are available elsewhere [10]. Briefly, all live births (births of 28 or more complete gestational weeks), all stillbirths of at least 20 weeks gestational age, and pregnancy terminations at any gestational age following the prenatal diagnosis of NTDs were included. We identified women who had an NTD-affected pregnancy in the period 2004–2015, and conducted a retrospective survey. We hypothesized that the NTD identified in the surveillance system was the first NTD pregnancy for the woman. If women appeared in the surveillance system a second time or more, we checked the date of the end of the pregnancy to determine which was the first NTD and then further pregnancies were identified as recurrent NTD pregnancies. NTDs included anencephaly (International Classification of Diseases, Tenth Revision, Clinical Modification, ICD-10-CM: 740.0), spina bifida (741.90), and encephalocele (742.0). A structured interview was administrated by a local health care provider, including the birth information of NTDs and recurrent NTDs, and dietary frequency and life style factors. The dietary frequency has been used in our previous study [27] and included the frequency of taking meat, sea food, eggs, milk, fresh vegetables, fresh fruits, legume and local pickled vegetable per week; life style factors included the frequency of tea drinking and passive smoking. An annual work meeting was held for staff who collected and reported data of surveillance system of every county, and the staffs were trained every year. The study protocol was reviewed and approved by the Institutional Review Board of Peking University.

Statistical analysis

NTDs were classified as “recurrent” if they affected the pregnancy of a mother with a prior NTD-affected pregnancy. NTDs included three major subtypes, namely, anencephaly, spina bifida, and encephalocele.

The prevalence of recurrent NTDs was calculated as the number of recurrent NTDs divided by the number of occurrent NTDs. Data on maternal age, body mass index (BMI) of women before the pregnancy, gestational weeks, education, and the occupation at the time the first NTDs occurred were collected, as were details about NTD types, sex, interval between the two NTDs, FA supplementation, and duration and dosage of FA. Dietary information was compared between affected women and controls. Statistical analyses were conducted using a t-test for comparison of maternal age, BMI, gestational weeks in groups; a Chi-square test were used for comparison of the categorical data, including maternal education, occupation, sex of offspring, FA supplementation information, et al. A two-tailed P ≤ 0.05 was considered statistically significant. All statistical analyses were performed using the SPSS package version 20.0 (SPSS Inc.).

Author contributions

Zhiwen Li designed research, Jufen Liu and Zhiwen Li conducted research, Jufen Liu analyzed the data and wrote the first draft of the manuscript, Hongtian Li and Aiguo Ren wrote and revised the draft, Nicholas D.E. Greene revised the draft and provided critical suggestions on the study plan. All authors read, reviewed and approved the final manuscript.

ACKNOWLEDGMENTS

This study was supported by grants from the National Natural Science Foundation of China (No. 81373014, No. 81511130088 and No. 81202265) and Medical Research Council (United Kingdom, N003713). NG is supported by the MRC and Great Ormond Street Hospital Children’s Charity.

CONFLICTS OF INTEREST

None declared.

REFERENCES

1. Grosse SD, Collins JS. Folic acid supplementation and neural tube defect recurrence prevention. Birth Defects Res A Clin Mol Teratol. 2007; 79:737-742.

2. Holmes-Siedle M, Lindenbaum RH, Galliard A. Recurrence of neural tube defect in a group of at risk women: a 10 year study of Pregnavite Forte F. J Med Genet. 1992; 29:134-135.

3. Sheppard S, Nevin NC, Seller MJ, Wild J, Smithells RW, Read AP, Harris R, Fielding DW, Schorah CJ. Neural tube defect recurrence after ‘partial’ vitamin supplementation. J Med Genet. 1989; 26:326-329.

4. Swerts A, Evers-Kiebooms G, Van den Berghe H. Pregnancies of mothers with a neural tube defect child: outcomes and recurrence risks. J Genet Hum. 1987; 35:339-349.

5. Cowchock S, Ainbender E, Prescott G, Crandall B, Lau L, Heller R, Muir WA, Kloza E, Feigelson M, Mennuti M, Cederquist L. The recurrence risk for neural tube defects in the United States: a collaborative study. Am J Med Genet. 1980; 5:309-314.

6. MRC Vitamin Study Research Group. Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group. Lancet. 1991; 338:131-137.

7. Li Z, Ren A, Zhang L, Ye R, Li S, Zheng J, Hong S, Wang T, Li Z. Extremely high prevalence of neural tube defects in a 4-county area in Shanxi Province, China. Birth Defects Res A Clin Mol Teratol. 2006; 76:237-240.

8. Moore CA, Li S, Li Z, Hong SX, Gu HQ, Berry RJ, Mulinare J, Erickson JD. Elevated rates of severe neural tube defects in a high-prevalence area in northern China. Am J Med Genet. 1997; 73:113-118.

9. Chen G, Pei LJ, Huang J, Song XM, Lin LM, Gu X, Wu JX, Wang F, Wu JL, Chen JP, Liu JF, Xin RL, Zhang T, Zheng XY. Unusual patterns of neural tube defects in a high risk region of northern China. Biomed Environ Sci. 2009; 22:340-344.

10. Liu J, Zhang L, Li Z, Jin L, Zhang Y, Ye R, Liu J, Ren A. Prevalence and trend of neural tube defects in five counties in Shanxi province of Northern China, 2000 to 2014. Birth Defects Res A Clin Mol Teratol. 2016; 106:267-274.

11. Morris JK, Wald NJ. Prevalence of neural tube defect pregnancies in England and Wales from 1964 to 2004. J Med Screen. 2007; 14:55-59.

12. Williams J, Mai CT, Mulinare J, Isenburg J, Flood TJ, Ethen M, Frohnert B, Kirby RS. Updated estimates of neural tube defects prevented by mandatory folic Acid fortification - United States, 1995-2011. MMWR Morb Mortal Wkly Rep. 2015; 64:1-5.

13. Wang Y, Wu Y, Zhou G, Xu C, Xiao K. An estimate of recurrence risk for neural tube defects in China. [Article in Chinese]. Hua Xi Yi Ke Da Xue Bao. 1996; 27:196-198.

14. Yen S, MacMahon B. Genetics of anencephaly and spina bifida? Lancet. 1968; 2:623-626.

15. Viswanathan M, Treiman KA, Kish-Doto J, Middleton JC, Coker-Schwimmer EJ, Nicholson WK. Folic acid supplementation for the prevention of neural tube defects: an updated evidence report and systematic review for the US preventive services task force. JAMA. 2017; 317:190-203.

16. Czeizel AE, Dudas I. Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med. 1992; 327:1832-1835.

17. Berry RJ, Li Z, Erickson JD, Li S, Moore CA, Wang H, Mulinare J, Zhao P, Wong LY, Gindler J, Hong SX, Correa A. 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; 341:1485-1490.

18. Zhang TN, Gong TT, Chen YL, Wu QJ, Zhang Y, Jiang CZ, Li J, Li LL, Zhou C, Huang YH. Time trends in the prevalence and epidemiological characteristics of neural tube defects in Liaoning Province, China, 2006-2015: a population-based study. Oncotarget. 2017; 8:17092-17104. https://doi.org/10.18632/oncotarget.15060.

19. Ren AG. Prevention of neural tube defects with folic acid: the Chinese experience. World J Clin Pediatr. 2015; 4:41-44.

20. Liu JF, Jin L, Meng QQ, Gao LL, Zhang L, Li ZW, Ren AG. Changes in folic acid supplementation behaviour among women of reproductive age after the implementation of a massive supplementation programme in China. Public Health Nutr. 2015; 18:582-588.

21. Werler MM, Shapiro S, Mitchell AA. Periconceptional folic acid exposure and risk of occurrent neural tube defects. JAMA. 1993; 269:1257-1261.

22. Smithells RW, Seller MJ, Harris R, Fielding DW, Schorah CJ, Nevin NC, Sheppard S, Read AP, Walker S, Wild J. Further experience of vitamin supplementation for prevention of neural-tube defect recurrences. Lancet. 1983; 1:1027-1031.

23. Bupp CP, Sarasua SM, Dean JH, Stevenson RE. When folic acid fails: Insights from 20 years of neural tube defect surveillance in South Carolina. Am J Med Genet A. 2015; 167a:2244-2250.

24. Huang HY, Chen HL, Feng LP. Maternal obesity and the risk of neural tube defects in offspring: a meta-analysis. Obes Res Clin Pract. 2017; 11:188-197.

25. Watkins ML, Rasmussen SA, Honein MA, Botto LD, Moore CA. Maternal obesity and risk for birth defects. Pediatrics. 2003; 111:1152-1158.

26. Li S, Moore CA, Li Z, Berry RJ, Gindler J, Hong SX, Liu Y, Mulinare J, Wong LY, Gu HQ, Erickson JD. A population-based birth defects surveillance system in the People’s Republic of China. Paediatr Perinat Epidemiol. 2003; 17:287-293.

27. Li ZW, Ren AG, Zhang L, Guo ZY, Jin YS, Li Z. [Dietary factors and the risk of neural tube defects: a case-control study in Shanxi province, China]. [Article in Chinese]. Zhonghua Liu Xing Bing Xue Za Zhi. 2006; 27:831-835.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 19890