RESUMEN
OBJECTIVE: To review the research progress on etiology and pathogenesis of spina bifida. METHODS: By consulting relevant domestic and foreign research literature on spina bifida, the classification, epidemic trend, pathogenesis, etiology, prevention and treatment of it were analyzed and summarized. RESULTS: Spina bifida, a common phenotype of neural tube defects, is classified based on the degree and pattern of malformation associated with neuroectodermal involvement and is due to the disturbance of neural tube closure 28 days before embryonic development. The prevalence of spina bifida varies greatly among different ethnic groups and regions, and its etiology is complex. Currently, some spina bifida patients can be prevented by folic acid supplements, and with the improvement of treatment technology, the short-term and long-term survival rate of children with spina bifida has improved. CONCLUSION: The research on the pathogenesis of spina bifida will be based on the refined individual information on exposure, genetics, and complex phenotype, and will provide a theoretical basis for improving prevention and treatment strategies through multidisciplinary cooperation.
Asunto(s)
Defectos del Tubo Neural , Disrafia Espinal , Femenino , Ácido Fólico , Humanos , Embarazo , Prevalencia , Disrafia Espinal/epidemiología , Disrafia Espinal/etiologíaRESUMEN
The International Clearinghouse for Birth Defects, Surveillance and Research reports a rise in the prevalence rate of spina bifida in Japan. We determined first-trimester folate status of Hokkaido women and identified potential predictors. Participants were 15 266 pregnant women of the Hokkaido Study on Environment and Children's Health Cohort. Data were extracted from self-reported questionnaires and biochemical assay results. Demographic determinants of low folate status were younger maternal age (adjusted OR (AOR) 1·48; 95 % CI 1·32, 1·66), lower educational level (AOR 1·27; 95 % CI 1·17, 1·39) and lower annual income (AOR 1·11; 95 % CI 1·01, 1·22). Plasma cotinine concentrations of 1·19-65·21 nmol/l increased the risk of low folate status (AOR 1·20; 95 % CI 1·10, 1·31) and concentrations >65·21 nmol/l further increased the risk (AOR 1·91; 95 % CI 1·70, 2·14). The most favourable predictor was use of folic acid (FA) supplements (AOR 0·19; 95 % CI 0·17, 0·22). Certain socio-demographic factors influence folate status among pregnant Japanese women. Modifiable negative and positive predictors were active and passive tobacco smoking and use of FA supplements. Avoiding both active and passive tobacco smoking and using FA supplements could improve the folate status of Japanese women.
Asunto(s)
Deficiencia de Ácido Fólico/etiología , Ácido Fólico/sangre , Estado Nutricional , Complicaciones del Embarazo/etiología , Disrafia Espinal/sangre , Complejo Vitamínico B/sangre , Adolescente , Adulto , Cotinina/sangre , Suplementos Dietéticos , Femenino , Ácido Fólico/uso terapéutico , Deficiencia de Ácido Fólico/sangre , Deficiencia de Ácido Fólico/prevención & control , Humanos , Japón , Embarazo , Complicaciones del Embarazo/sangre , Primer Trimestre del Embarazo , Atención Prenatal , Factores de Riesgo , Autoinforme , Fumar/efectos adversos , Factores Socioeconómicos , Disrafia Espinal/etiología , Encuestas y Cuestionarios , Contaminación por Humo de Tabaco/efectos adversos , Complejo Vitamínico B/uso terapéutico , Adulto JovenRESUMEN
This study was conducted to assess the association between the risks of spina bifida (SB) in relation to cigarette, alcohol, and caffeine consumption by women during the first month of pregnancy. Between 1988-2012, this multi-center case-control study interviewed mothers of 776 SB cases and 8,756 controls about pregnancy events and exposures. We evaluated cigarette smoking, frequency of alcohol drinking, and caffeine intake during the first lunar month of pregnancy in relation to SB risk. Logistic regression models were used to calculate adjusted odds ratios and 95% confidence intervals. Levels of cigarette smoking (1-9 and ≥10/day), alcohol intake (average ≥4 drinks/day) and caffeine intake (<1, 1, and ≥2 cups/day) were not likely to be associated with increased risk of SB. Further, results were similar among women who ingested less than the recommended amount of folic acid (400 µg/day).
Asunto(s)
Consumo de Bebidas Alcohólicas/efectos adversos , Cafeína/efectos adversos , Ácido Fólico/administración & dosificación , Fumar/efectos adversos , Disrafia Espinal/epidemiología , Disrafia Espinal/etiología , Adolescente , Adulto , Estudios de Casos y Controles , Café/efectos adversos , Femenino , Humanos , Modelos Logísticos , Embarazo , Primer Trimestre del Embarazo , Factores de Riesgo , Adulto JovenRESUMEN
OBJECTIVES: To evaluate whether a relationship exists between season at conception and occurrence of isolated spina bifida (ISB). STUDY DESIGN: All fetuses with prenatal diagnosis of ISB were analyzed according to date of conception. We compared the seasonal rates of conception between ISB fetuses and a control group consisting of a cohort of fetuses delivered during the same period from 1992 to 2009. RESULTS: In the control group, conceptions were equally distributed among the four seasons. Chi-square analysis showed a significantly higher rate of ISB conceptions in the fall compared with the control group (16/36, 44% vs. 12467/50533, 25%, Odds Ratio (OR) 2.44, 95% confidence interval 1.21-4.92). Not a single woman with a fetus affected by ISB took preconceptional supplement of folic acid. CONCLUSIONS: Seasonality affects the frequency of ISB. We hypothesize that the seasonal differences may reflect dietary and climate changes with reduced intake of folic acid in the fall.
Asunto(s)
Fertilización/fisiología , Estaciones del Año , Disrafia Espinal/epidemiología , Disrafia Espinal/etiología , Estudios de Casos y Controles , Femenino , Humanos , Embarazo , Diagnóstico Prenatal , Prevalencia , Factores de Riesgo , Disrafia Espinal/diagnósticoRESUMEN
OBJECTIVE: The purpose of this study was to investigate the relationship between spina bifida and 2 established risk factors (pregestational diabetes mellitus and obesity) in both the presence and absence of the recommended daily folic acid intake in the periconceptional period. STUDY DESIGN: Cases of spina bifida (n = 1154) and control subjects (n = 9439) from the Slone Epidemiology Center Birth Defects Study (1976-2011) were included. Information on preexisting diabetes mellitus (collected 1976-2011) and obesity (collected 1993-2011), defined as a body mass index of ≥30 kg/m(2), was collected through interviews that were conducted within 6 months of delivery. Periconceptional folic acid intake was calculated with both dietary and supplement information. Mothers were classified as consuming more or less than 400 µg/day of folic acid; food folate was included at a 30% discount for its lower bioavailability. Logistic regression models that were adjusted for maternal age, race, education, and study site were used to calculate adjusted odds ratios (aORs) and 95% confidence intervals (CIs) for the joint effects of low folic acid intake coupled with diabetes mellitus or obesity. RESULTS: Case mothers were more likely to have diabetes mellitus or be obese (0.7% and 19.0%, respectively) than control mothers (0.4% and 10.8%, respectively). The joint effect of diabetes mellitus and lower folic acid intake on spina bifida was larger (aOR, 3.95; 95% CI, 1.56-10.00) than that of diabetes mellitus and higher folic acid intake (aOR, 1.31; 95% CI, 0.17-10.30). Folic acid intake made little difference on the association between obesity and spina bifida. CONCLUSION: Our findings suggest that folic acid further attenuates, although does not eliminate, the risk of spina bifida that is associated with diabetes mellitus than the risk with obesity.
Asunto(s)
Complicaciones de la Diabetes/etiología , Ácido Fólico/administración & dosificación , Obesidad/complicaciones , Disrafia Espinal/etiología , Adulto , Estudios de Casos y Controles , Femenino , Humanos , Modelos Logísticos , Factores de RiesgoRESUMEN
BACKGROUND: Recognized risk factors for neural tube defects (NTDs) poorly predict population-level NTD risk. However, the proportion of NTDs that can be attributed to these risk factors is uncertain. METHODS: To determine the proportion of NTD cases that is attributable to known or suspected risk factors (i.e., female infant sex, family history of NTDs, and maternal Hispanic ethnicity, obesity, pregestational diabetes, gestational diabetes, low dietary folate intake, lack of folic acid supplementation, anticonvulsant use, and hot tub or sauna use), we estimated the adjusted population attributable fraction (aAF) for each factor, using the method of Eide and Geffler and data from the National Birth Defects Prevention Study. RESULTS: Our analyses of these data indicate that the proportion of cases of spina bifida and anencephaly that can be attributed to known risk factors is 28% and 44%, respectively. For spina bifida, the factor with the greatest attributable fraction was maternal obesity (aAF, 10%), whereas for anencephaly it was Hispanic ethnicity (aAF, 15%). CONCLUSION: Our analyses indicate that known risk factors account for <50% of NTD cases. Hence, the majority of NTD cases are attributable to, as yet, unidentified factors. These findings highlight the need for continued research to identify genetic and additional nongenetic risk factors for NTDs. Further, these findings suggest that strategies that aim to reduce the risk of NTDs associated with maternal Hispanic ethnicity and obesity may have the greatest impact on the population prevalence of these conditions.
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Anencefalia/epidemiología , Complicaciones del Embarazo , Disrafia Espinal/epidemiología , Adulto , Anencefalia/etiología , Causalidad , Bases de Datos Factuales , Femenino , Hispánicos o Latinos/etnología , Humanos , Masculino , Exposición Materna , Madres , Obesidad/complicaciones , Obesidad/epidemiología , Embarazo , Medición de Riesgo , Factores de Riesgo , Disrafia Espinal/etiología , Estados Unidos/epidemiologíaRESUMEN
Neural tube defects (NTDs) such as spina bifida and anencephaly are some of the most common structural birth defects found in humans. These defects occur due to failures of neurulation, a process where the flat neural plate rolls into a tube. In spite of their prevalence, the causes of NTDs are poorly understood. The multifactorial threshold model best describes the pattern of inheritance of NTDs where multiple undefined gene variants interact with environmental factors to cause an NTD. To date, mouse models have implicated a multitude of genes as required for neurulation, providing a mechanistic understanding of the cellular and molecular pathways that control neurulation. However, the majority of these mouse models exhibit NTDs with a Mendelian pattern of inheritance. Still, many examples of multifactorial inheritance have been demonstrated in mouse models of NTDs. These include null and hypomorphic alleles of neurulation genes that interact in a complex fashion with other genetic mutations or environmental factors to cause NTDs. These models have implicated several genes and pathways for testing as candidates for the genetic basis of NTDs in humans, resulting in identification of putative pathogenic mutations in some patients. Mouse models also provide an experimental paradigm to gain a mechanistic understanding of the environmental factors that influence NTD occurrence, such as folic acid and maternal diabetes, and have led to the discovery of additional preventative nutritional supplements such as inositol. This review provides examples of how multifactorial inheritance of NTDs can be modeled in the mouse.
Asunto(s)
Modelos Animales de Enfermedad , Predisposición Genética a la Enfermedad , Herencia Multifactorial , Defectos del Tubo Neural/etiología , Defectos del Tubo Neural/genética , Anencefalia/etiología , Anencefalia/genética , Animales , Ácido Fólico/metabolismo , Humanos , Ratones , Disrafia Espinal/etiología , Disrafia Espinal/genéticaRESUMEN
Studies have demonstrated that catechin, an antioxidant found in tea, can reduce the bioavailability of folate. Because periconceptional folic acid intake has been demonstrated to reduce the risk of spina bifida, tea consumption may put pregnant women at risk because of its possible antifolate properties. Using data collected in the Slone Epidemiology Center Birth Defects Study, we examined whether tea consumption during early pregnancy was associated with an increased risk of spina bifida. Mothers of 518 spina bifida cases and 6424 controls were interviewed within 6 months after delivery about pregnancy events and exposures. Data on tea intake were collected during three periods (1976-1988, 1998-2005 and 2009-2010). Logistic regression models were used to calculate odds ratios (ORs) and 95% confidence intervals (CIs), adjusted for study center. Intake of both periconceptional food folate and diet and supplemental folic acid were examined as a potential effect modifier. For 1976 to 1988, ORs were not elevated for daily tea intake. For 1998 and onward, ORs were also close to 1.0, but there was a modest increase for those who drank more than 3 cups/day (OR, 1.92; 95% CI, 0.84-4.38). Among women with total folic acid intake greater than 400 µg, consumption of 3 cups or more of tea per day was associated with an increased risk of spina bifida in 1976 to 1988 (OR, 2.04; 95% CI, 0.69-7.66) and in the later periods (OR, 3.13; 95% CI, 0.87-11.33). Our data do not support an overall association between tea consumption and spina bifida, but there is a suggestion of a possible interaction between higher levels of folic acid intake and tea consumption.
Asunto(s)
Conducta de Ingestión de Líquido/fisiología , Fenómenos Fisiologicos Nutricionales Maternos , Primer Trimestre del Embarazo , Disrafia Espinal/etiología , Té , Adulto , Estudios de Casos y Controles , Encuestas sobre Dietas , Femenino , Humanos , Recién Nacido , Embarazo , Primer Trimestre del Embarazo/fisiología , Factores de Riesgo , Disrafia Espinal/epidemiología , Adulto JovenRESUMEN
Lumbosacral spina bifida is a common debilitating birth defect whose multiple causes are poorly understood. Here, we provide the first genetic delineation of cholinergic nicotinic receptor alpha7 (Chrna7) expression and link the ablation of the Chrna7 cell lineage to this condition in the mouse. Using homologous recombination, an IRES-Cre bi-cistronic cassette was introduced into the 3' noncoding region of Chrna7 (Chrna7:Cre) for identifying cell lineages expressing this gene. This lineage first appears at embryonic day E9.0 in rhombomeres 3 and 5 of the neural tube and extends to cell subsets in most tissues by E14.5. Ablation of the Chrna7:Cre cell lineage in embryos from crosses with conditionally expressed attenuated diphtheria toxin results in precise developmental defects including omphalocele (89%) and open spina bifida (SB; 80%). We hypothesized that like humans, this defect would be modified by environmental compounds not only folic acid or choline but also nicotine. Prenatal chronic oral nicotine administration substantially worsened the defect to often include the rostral neural tube. In contrast, supplementation of the maternal diet with 2% choline decreased SB prevalence to 38% and dramatically reduced the defect severity. Folic acid supplementation only trended towards a reduced SB frequency. The omphalocele was unaffected by these interventions. These studies identify the Chrna7 cell lineage as participating in posterior neuropore closure and present a novel model of lower SB that can be substantially modified by the prenatal environment.
Asunto(s)
Linaje de la Célula , Colina/farmacología , Nicotina/farmacología , Receptores Nicotínicos/metabolismo , Disrafia Espinal/etiología , Animales , Femenino , Recombinación Homóloga , Ratones , Embarazo , Efectos Tardíos de la Exposición Prenatal , Receptores Nicotínicos/deficiencia , Disrafia Espinal/genética , Disrafia Espinal/patología , Receptor Nicotínico de Acetilcolina alfa 7RESUMEN
PURPOSE: Neural tube defects, including spina bifida and anencephaly, are the second most common birth defects with an incidence in Italy of 0.4-1/1,000. Information on factors playing a role in the pathogenesis of spina bifida is based on populations with different exposures, lifestyle, social and cultural habits compared to Italian people. Our objective was to fill this gap by using data from a case-control interview study carried out at the G. Gaslini Children's Hospital, Genoa, from 2000 to 2008. METHODS: We surveyed questionnaires from 133 case mothers and 273 control women providing information on periconceptional risk factors. Univariate and multivariate logistic regression analyses were used to estimate risks by odds ratios (ORs) and 95% confidence intervals (95% CIs). RESULTS: Univariate results suggest that birth order, low maternal educational level, age, smoking habits, alcohol consumption, high caffeine intake, lack of folate supplementation, low and high calorie diet, occasional consumption of fruit and vegetables, high emotional stress, and environmental pollution are associated with an increased spina bifida risk. Nevertheless, high caffeine intake (OR = 10.82; 95% CI, 3.78-31), low calorie diet (OR = 5.15; 95%CI, 1.79-14), occasional consumption of fruit and vegetables (OR = 3.38; 95% CI, 1.67-6.82), alcohol consumption (OR = 3.05; 95% CI, 1.24-7.50) and, above all, lack of folate supplementation at any time of pregnancy (OR = 20.54; 95% CI, 5.41-77) mainly determined spina bifida risk in the multivariate analysis. CONCLUSION: Our findings point out that a common underlying mechanism, a disturbed folate/homocysteine metabolism, may be causative for the burden of spina bifida in the Italian population.
Asunto(s)
Estilo de Vida , Efectos Tardíos de la Exposición Prenatal/epidemiología , Disrafia Espinal/epidemiología , Disrafia Espinal/etiología , Adulto , Consumo de Bebidas Alcohólicas/efectos adversos , Estudios de Casos y Controles , Dieta , Suplementos Dietéticos , Femenino , Ácido Fólico/uso terapéutico , Humanos , Italia/epidemiología , Edad Materna , Análisis Multivariante , Oportunidad Relativa , Embarazo , Factores de Riesgo , Fumar/efectos adversos , Factores Socioeconómicos , Encuestas y Cuestionarios , Complejo Vitamínico B/uso terapéuticoRESUMEN
This paper presents the trend of spina bifida and other neural tube defects in Oman after the nationwide implementation of folate supplementation of pregnant women in 1990 and the fortification of wheat flour with iron and folate in 1996. The annual incidence of spina bifida fluctuated from 2.34 to 4.03 per 1000 deliveries between 1991 and 1996, but fell sharply to 2.11 per 1000 deliveries in 1997, after which the downward trend continued, reaching 0.29 per 1000 deliveries by 2006. The rate of other neural tube defects remained almost constant. The reduction in spina bifida rates in Oman could be linked to the start of flour fortification but not the supplementation programme.
Asunto(s)
Harina , Ácido Fólico/uso terapéutico , Alimentos Fortificados , Defectos del Tubo Neural/prevención & control , Disrafia Espinal/prevención & control , Complejo Vitamínico B/uso terapéutico , Encuestas sobre Dietas , Femenino , Hematínicos/uso terapéutico , Humanos , Incidencia , Hierro/uso terapéutico , Morbilidad , Programas Nacionales de Salud/organización & administración , Defectos del Tubo Neural/epidemiología , Defectos del Tubo Neural/etiología , Política Nutricional , Omán/epidemiología , Embarazo , Resultado del Embarazo/epidemiología , Evaluación de Programas y Proyectos de Salud , Disrafia Espinal/epidemiología , Disrafia Espinal/etiologíaRESUMEN
BACKGROUND: Low folate and high homocysteine (Hcy) concentrations are associated with pregnancy-related pathologies such as spina bifida. Polymorphisms in folate/Hcy metabolic enzymes may contribute to this potentially pathogenic biochemical phenotype. METHODS: The study comprised 26 Caucasian and 23 African-American premenopausal women. Subjects gave fasting blood samples for biochemical phenotyping and genotyping. Total Hcy (tHcy) and both plasma and red blood cell (RBC) folate derivatives (i.e. tetrahydrofolate [THF], 5-methylTHF [5-MTHF], and 5,10-methenylTHF [5,10-MTHF]) were measured using stable isotope dilution liquid chromatography, multiple reaction monitoring, and mass spectrometry. Eleven polymorphisms from nine folate/Hcy pathway genes were genotyped. Tests of association between genetic, lifestyle, and biochemical variables were applied. RESULTS: In African American women, tHcy concentrations were associated (p < 0.05) with total RBC folate, RBC 5-MTHF, B(12), and polymorphisms in methionine synthase (MTR) and thymidylate synthase (TYMS). In Caucasian women, tHcy concentrations were not associated with total folate levels, but were associated (p < 0.05) with RBC THF, ratios of RBC 5-MTHF:THF, and polymorphisms in 5,10-methylenetetrahydrofolate reductase (MTHFR) and MTR. In African Americans, folate derivative levels were associated with smoking, B(12), and polymorphisms in MTR, TYMS, methionine synthase reductase (MTRR), and reduced folate carrier1 (RFC1). In Caucasians, folate derivative levels were associated with vitamin use, B(12), and polymorphisms in MTHFR, TYMS, and RFC1. CONCLUSIONS: Polymorphisms in the folate/Hcy pathway are associated with tHcy and folate derivative levels. In African American and Caucasian women, different factors are associated with folate/Hcy phenotypes and may contribute to race-specific differences in the risks of a range of pregnancy-related pathologies.
Asunto(s)
Homocisteína/sangre , Estilo de Vida , Premenopausia/metabolismo , 5-Metiltetrahidrofolato-Homocisteína S-Metiltransferasa/genética , Adolescente , Adulto , Negro o Afroamericano/genética , Niño , Preescolar , Suplementos Dietéticos , Eritrocitos/química , Femenino , Estudios de Asociación Genética , Homocisteína/genética , Humanos , Lactante , Proteínas de Transporte de Membrana/genética , Metilenotetrahidrofolato Reductasa (NADPH2)/genética , Persona de Mediana Edad , Polimorfismo Genético , Embarazo , Premenopausia/genética , Disrafia Espinal/epidemiología , Disrafia Espinal/etiología , Disrafia Espinal/genética , Disrafia Espinal/metabolismo , Tetrahidrofolatos/análisis , Timidilato Sintasa/genética , Vitaminas/administración & dosificación , Población Blanca/genética , Adulto JovenRESUMEN
Las malformaciones congénitas constituyen la segunda causa de mortalidad infantil en nuestro medio, lo cual significa que nuestro comportamiento en términos de salud pública, es muy similar a los países desarrollados. Hay malformaciones de alto costo médico social en las cuales afortunadamente se puede intervenir eficazmente con medidas de prevención primaria o secundaria. Los defectos del tubo neural son una de ellas y en el mundo curiosamente, no son muchos los países que lo hacen. Afortunadamente, Chile ha tenido una actitud pionera en América con la implementación de un programa de fortificación de harinas que ha significado una disminución cercana al 50 por ciento en las tasas de frecuencia de la enfermedad. Los mecanismos bioquímicos exactos de la prevención no están claramente descritos, pero un papel importante juega el ácido fólico en la síntesis del ADN y en el metabolismo de la metionina/homocisteina, vías metabólicas claves del neuro desarrollo inicial. Lo más importante sin embargo, es que la prevención actúa sólo para aquellos casos típicamente dependientes de la neurulacion primaria y no para todos los defectos cráneo encefálicos.
Congenital anomalies are the second cause of infant mortality in Chile, which is similar to the findings in developed countries. The medical-social burden of some of these malformations is high, but some of them are able to undergo primary or secondary prevention. Neural tube defects are among them and unfortunately, a. global prevention is not the rule. Chile has been one of the pioneer countries with supplementation of folic acid fortification, which has resulted in a reduction in the prevalence of open neural tube defects in about 50 percent. The exact mechanisms involved in the prevention of open neural tube defects are not clear, but an important role has been ascribed to folic acid in the synthesis of DNA and metabolism of metionin-homocistein, key pathways for the early development of the neural tube. An important point is that fortification with folic acid only works in those defects associated with the primary neurulation and not to all cranio-encephalic defects.
Asunto(s)
Humanos , Femenino , Embarazo , Recién Nacido , Defectos del Tubo Neural/diagnóstico , Defectos del Tubo Neural/fisiopatología , Defectos del Tubo Neural/metabolismo , Diagnóstico Prenatal , Ácido Fólico/metabolismo , Anencefalia/etiología , Defectos del Tubo Neural/epidemiología , Disrafia Espinal/etiología , Homocisteína/metabolismo , Metionina/metabolismo , Factores de RiesgoRESUMEN
Mandatory vitamin B12 fortification of enriched grain products is long overdue in the United States and Canada. Fortification would help provide the 2.4 mug of synthetic vitamin B12 that the US Institute of Medicine recommends for all persons 50 years and older. The findings of Ray and colleagues in this issue suggest that B12 may also help to prevent neural tube defects. If recommendations for B12 fortification were followed, it is possible that cases of spina bifida and anencephaly would be prevented. Two hundred twenty thousand children each year acquire folic acid-preventable spina bifida because many governments, including all in Europe, have yet to implement mandatory folic acid fortification. Fortification with folic acid and vitamin B12 is safe and should be implemented in all countries.
Asunto(s)
Ácido Fólico/administración & dosificación , Alimentos Fortificados , Disrafia Espinal/prevención & control , Vitamina B 12/administración & dosificación , Complejo Vitamínico B/administración & dosificación , Adulto , Canadá/epidemiología , Femenino , Harina , Humanos , Defectos del Tubo Neural/epidemiología , Defectos del Tubo Neural/etiología , Defectos del Tubo Neural/prevención & control , Embarazo , Disrafia Espinal/epidemiología , Disrafia Espinal/etiología , Estados Unidos/epidemiología , United States Food and Drug Administration , Deficiencia de Vitamina B 12/complicacionesRESUMEN
Spina bifida, anencephaly, and encephalocele are commonly grouped together and termed neural tube defects (NTD). Failure of closure of the neural tube during development results in anencephaly or spina bifida aperta but encephaloceles are possibly post-closure defects. NTD are associated with a number of other central nervous system (CNS) and non-neural malformations. Racial, geographic and seasonal variations seem to affect their incidence. Etiology of NTD is unknown. Most of the non-syndromic NTD are of multifactorial origin. Recent in vitro and in vivo studies have highlighted the molecular mechanisms of neurulation in vertebrates but the morphologic development of human neural tube is poorly understood. A multisite closure theory, extrapolated directly from mouse experiments highlighted the clinical relevance of closure mechanisms to human NTD. Animal models, such as circle tail, curly tail, loop tail, shrm and numerous knockouts provide some insight into the mechanisms of NTD. Also available in the literature are a plethora of chemically induced preclosure and a few post-closure models of NTD, which highlight the fact that CNS malformations are of hetergeneitic nature. No Mendelian pattern of inheritance has been reported. Association with single gene defects, enhanced recurrence risk among siblings, and a higher frequency in twins than in singletons indicate the presence of a strong genetic contribution to the etiology of NTD. Non-availability of families with a significant number of NTD cases makes research into genetic causation of NTD difficult. Case reports and epidemiologic studies have implicated a number of chemicals, widely differing therapeutic drugs, environmental contaminants, pollutants, infectious agents, and solvents. Maternal hyperthermia, use of valproate by epileptic women during pregnancy, deficiency and excess of certain nutrients and chronic maternal diseases (e.g. diabetes mellitus) are reported to cause a manifold increase in the incidence of NTD. A host of suspected teratogens are also available in the literature. The UK and Hungarian studies showed that periconceptional supplementation of women with folate (FA) reduces significantly both the first occurrence and recurrence of NTD in the offspring. This led to mandatory periconceptional FA supplementation in a number of countries. Encouraged by the results of clinical studies, numerous laboratory investigations focused on the genes involved in the FA, vitamin B12 and homocysteine metabolism during neural tube development. As of today no clinical or experimental study has provided unequivocal evidence for a definitive role for any of these genes in the causation of NTD suggesting that a multitude of genes, growth factors and receptors interact in controlling neural tube development by yet unknown mechanisms. Future studies must address issues of gene-gene, gene-nutrient and gene-environment interactions in the pathogenesis of NTD.
Asunto(s)
Defectos del Tubo Neural/etiología , Defectos del Tubo Neural/genética , Defectos del Tubo Neural/prevención & control , Anencefalia/etiología , Animales , Desarrollo Embrionario , Encefalocele/etiología , Femenino , Ácido Fólico/uso terapéutico , Predisposición Genética a la Enfermedad , Humanos , Masculino , Modelos Anatómicos , Modelos Biológicos , Cresta Neural/embriología , Embarazo , Disrafia Espinal/etiologíaRESUMEN
Spina bifida results from failure of fusion of the caudal neural tube, and is one of the most common malformations of human structure. The causes of this disorder are heterogeneous and include chromosome abnormalities, single gene disorders, and teratogenic exposures. However, the cause is not known in most cases. Up to 70% of spina bifida cases can be prevented by maternal, periconceptional folic acid supplementation. The mechanism underlying this protective effect is unknown, but it is likely to include genes that regulate folate transport and metabolism. Individuals with spina bifida need both surgical and medical management. Although surgical closure of the malformation is generally done in the neonatal period, a randomised clinical trial to assess in utero closure of spina bifida has been initiated in the USA. Medical management is a lifelong necessity for individuals with spina bifida, and should be provided by a multidisciplinary team.
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Disrafia Espinal , Animales , Femenino , Terapias Fetales , Humanos , Embarazo , Diagnóstico Prenatal , Factores de Riesgo , Disrafia Espinal/diagnóstico , Disrafia Espinal/etiología , Disrafia Espinal/genética , Disrafia Espinal/prevención & controlAsunto(s)
Deficiencia de Ácido Fólico/prevención & control , Ácido Fólico/administración & dosificación , Abastecimiento de Alimentos/legislación & jurisprudencia , Alimentos Fortificados/normas , Adulto , Anencefalia/etiología , Anencefalia/prevención & control , Femenino , Deficiencia de Ácido Fólico/complicaciones , Humanos , Recién Nacido , Nueva Zelanda , Embarazo , Disrafia Espinal/etiología , Disrafia Espinal/prevención & controlAsunto(s)
Anencefalia/epidemiología , Dieta/normas , Leucovorina/administración & dosificación , Disrafia Espinal/epidemiología , Anencefalia/etiología , Anencefalia/prevención & control , Suplementos Dietéticos/estadística & datos numéricos , Brotes de Enfermedades/prevención & control , Brotes de Enfermedades/estadística & datos numéricos , Femenino , Deficiencia de Ácido Fólico/complicaciones , Deficiencia de Ácido Fólico/prevención & control , Humanos , Recién Nacido , Embarazo , Complicaciones del Embarazo/prevención & control , Disrafia Espinal/etiología , Disrafia Espinal/prevención & controlRESUMEN
NTDs, resulting from failure of the neural tube to close during the fourth week of embryogenesis, are the most common severely disabling birth defects in the United States, with a frequency of approximately 1 of every 2000 births. Neural tube malformations involving the spinal cord and vertebral arches are referred to as spina bifida, with severe types of spina bifida involving protrusion of the spinal cord and/or meninges through a defect in the vertebral arch. Depending on the level of the lesion, interruption of the spinal cord at the site of the spina bifida defect causes paralysis of the legs, incontinence of urine and feces, anesthesia of the skin, and abnormalities of the hips, knees, and feet. Two additional abnormalities often seen in children with spina bifida include hydrocephalus and the Arnold-Chiari type II malformation. Despite the physical and particular learning disabilities children with spina bifida must cope with, participation in individualized educational programs can allow these children to develop skills necessary for autonomy in adulthood. Advances in research to uncover the molecular basis of NTDs is enhanced by knowledge of the link between both the environmental and genetic factors involved in the etiology of NTDs. The most recent development in NTD research for disease-causing genes is the discovery of a genetic link to the most well-known environmental cause of neural tube malformation, folate deficiency in pregnant women. Nearly a decade ago, periconceptional folic acid supplementation was proven to decrease both the recurrence and occurrence of NTDs. The study of folate and its association with NTDs is an ongoing endeavor that has led to numerous studies of different genes involved in the folate metabolism pathway, including the most commonly studied thermolabile mutation (C677T) in the MTHFR gene. An additional focus for NTD research involves mouse models that exhibit both naturally occurring NTDs, as well as those created by experimental design. We hope the search for genes involved in the risk and/or development of NTDs will lead to the development of strategies for prevention and treatment. The most recent achievement in treatment of NTDs involves the repair of meningomyelocele through advancements in fetal surgery. Convincing experimental evidence exists that in utero repair preserves neurologic function, as well as resolving the hydrocephalus and Arnold-Chiari malformation that often accompany meningomyelocele defects. However, follow-up is needed to completely evaluate long-term neurologic function and overall improved quality of life. And in the words of Olutoye and Adzick, "until the benefits of fetal [meningomyelocele] repair are carefully elucidated, weighed against maternal and fetal risks, and compared to conventional postnatal therapy, this procedure should be restricted to a few centers that are committed (clinically and experimentally) to investigating these issues."
Asunto(s)
Defectos del Tubo Neural , Disrafia Espinal , Animales , Parto Obstétrico/métodos , Modelos Animales de Enfermedad , Femenino , Ácido Fólico/metabolismo , Ácido Fólico/uso terapéutico , Deficiencia de Ácido Fólico/complicaciones , Deficiencia de Ácido Fólico/prevención & control , Predisposición Genética a la Enfermedad/genética , Humanos , Recién Nacido , Exposición Materna/efectos adversos , Metilenotetrahidrofolato Reductasa (NADPH2) , Ratones , Biología Molecular , Mutación/genética , Defectos del Tubo Neural/clasificación , Defectos del Tubo Neural/diagnóstico , Defectos del Tubo Neural/epidemiología , Defectos del Tubo Neural/etiología , Defectos del Tubo Neural/terapia , Oxidorreductasas actuantes sobre Donantes de Grupo CH-NH/genética , Embarazo , Atención Prenatal/métodos , Diagnóstico Prenatal/métodos , Factores de Riesgo , Disrafia Espinal/clasificación , Disrafia Espinal/diagnóstico , Disrafia Espinal/epidemiología , Disrafia Espinal/etiología , Disrafia Espinal/terapiaRESUMEN
We review the data from studies of mouse mutants that lend insight to the mechanisms that lead to neural tube defects (NTDs). Most of the 50 single-gene mutations that cause neural tube defects (NTDs) in mice also cause severe embryonic-lethal syndromes, in which exencephaly is a nonspecific feature. In a few mutants (e.g., Trp53, Macs, Mlp or Sp), other defects may be present, but affected fetuses can survive to birth. Multifactorial genetic causes, as are present in the curly tail stock (15-20% spina bifida), or the SELH/Bc strain (15-20% exencephaly), lead to nonsyndromic NTDs. The mutations indicate that "spina bifida occulta," a dorsal gap in the vertebral arches over an intact neural tube, is usually genetically and developmentally unrelated to exencephaly or "spina bifida" (aperta). Almost all exencephaly or spina bifida aperta of genetic origin is caused by failure of neural fold elevation. The developmental mechanisms in genetic NTDs are considered in terms of distinct rostro-caudal zones along the neural folds that likely differ in mechanism of elevation. Failure of elevation leads to: split face (zone A), exencephaly (zone B), rachischisis (all of zone D), or spina bifida (caudal zone D). The developmental mechanisms leading to these genetic NTDs are heterogeneous, even within one zone. At the tissue level, the mutants show that the mechanism of failure of elevation can involve, e.g., (1) slow growth of adjacent tethered tissue (curly tail), (2) defective forebrain mesenchyme (Cart1 or twist), (3) defective basal lamina in surface ectoderm (Lama5), (4) excessive breadth of floorplate and notochord (Lp), (5) abnormal neuroepithelium (Apob, Sp, Tcfap2a), (6) morphological deformation of neural folds (jmj), (7) abnormal neuroepithelial and neural crest cell gap-junction communication (Gja1), or (8) incomplete compensation for a defective step in the elevation sequence (SELH/Bc). At the biochemical level, mutants suggest involvement of: (1) faulty regulation of apoptosis (Trp53 or p300), (2) premature differentiation (Hes1), (3) disruption of actin function (Macs or Mlp), (4) abnormal telomerase complex (Terc), or (5) faulty pyrimidine synthesis (Sp). The NTD preventative effect of maternal dietary supplementation is also heterogeneous, as demonstrated by: (1) methionine (Axd), (2) folic acid or thymidine (Sp), or (3) inositol (curly tail). The heterogeneity of mechanism of mouse NTDs suggests that human NTDs, including the common nonsyndromic anencephaly or spina bifida, may also reflect a variety of genetically caused defects in developmental mechanisms normally responsible for elevation of the neural folds.