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1.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao ; 39(6): 785-791, 2017 Dec 20.
Artigo em Inglês | MEDLINE | ID: mdl-29338823

RESUMO

Objective To investigate the relationship between the methylation level of transcription starts site (TSS) upper stream of homeobox gene and the neural tube defects (NTDs). Methods A case-control study of two stages was designed. In the first stage,10 cases and 8 controls were extracted,in whom Illumina Infinium Human Methylation 450 k genome-wide beadchip was used for the quantification of DNA methylation levels of brain and spinal tissue. In the second stage,differentially methylated region within HOXA5 gene was detected with a larger numbers of samples (52 cases and 23 controls). DNA of brain or spinal tissue was extracted,and Matrix-assisted laser desorption ionization time-of-flight mass spectrometry technique of MassARRAY platform was employed for the validation of differentially methylated region of HOXA5 gene. Results In the first stage,27 CpG sites within TSS region of HOXA5 gene were found to be significantly hyper-methylated in case group compared to control group (P<0.05). In the second stage,a total of 10 CpG sites were analyzable within the differentially methylated region in the first stage. In the NTD case group,spinal bifida subgroup,and anencephaly subgroup,there were 7,6,and 2 sites with significantly higher methylation levels than that of control group (P<0.05). The average methylation level of TSS upper stream region within HOXA5 gene was higher in case group than control group [case group:(31.3±13.9)%,control group:(21.4±9.7)%],and the odds ratio after adjusting gender of fetus and pregnant week was 1.09 (1.03-1.16). Conclusion Hypermethylation within TSS upper stream region of HOXA5 gene in fetus is associated with a higher risk of NTDs.


Assuntos
Defeitos do Tubo Neural , Estudos de Casos e Controles , Ilhas de CpG , Metilação de DNA , Feminino , Genoma Humano , Proteínas de Homeodomínio , Humanos , Gravidez , Transcrição Gênica
2.
Beijing Da Xue Xue Bao Yi Xue Ban ; 46(3): 483-7, 2014 Jun 18.
Artigo em Chinês | MEDLINE | ID: mdl-24943034

RESUMO

OBJECTIVE: To establish and evaluate a newly established method of enzyme-linked immunosorbent assay (ELISA) for measuring human autoantibody to folate receptor (FR). METHODS: Folate receptor was extracted and purified from healthy woman placenta tissues. The protein was coated on 96-well plates. Goat monoclonal antibody was used as detecting antibody to set up the indirect ELISA procedure. The sensitivity, precision and linearity of the method were evaluated. Further, the method was compared with the ELISA method with commercialized bovine folate binding protein (FBP) by determining autoantibody levels in 24 individuals. RESULTS: The measuring range of the standard curve was from 6.25 × 10⁻4 to 8 × 10⁻² (the IgG concentration of pooled plasma from healthy donors was defined as 1). The lowest detectable level was 3.13 × 10⁻4. The intra- and inter-assay coefficients of variations were 2.74%-8.07% and 4.16%-8.23%, respectively. Linearity test results were considered within acceptable limits. The data from FBP-ELISA and FR-ELISA were highly correlated (r=0.954, P<0.001); The value from FR-ELISA was higher by 14% than that from FBP-ELISA. CONCLUSION: The ELISA method for measuring human autoantibody IgG to folate receptor was successfully established using human FR as coating protein. The method is sensitive and repeatable and can be used in large-scale population study.


Assuntos
Autoanticorpos/sangue , Ensaio de Imunoadsorção Enzimática/métodos , Receptores de Folato com Âncoras de GPI/imunologia , Imunoglobulina G/sangue , Anticorpos Monoclonais , Feminino , Humanos
3.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao ; 36(4): 410-4, 2014 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-25176210

RESUMO

OBJECTIVE: To establish the method of enzyme-linked immunosorbent assay (ELISA) for measuring human IgM autoantibody to folate receptor. METHODS: Folate receptor was extracted and purified from the healthy woman placenta. The protein was coated on 96-well plates with a concentration of 5 ng/Μl. Goat monoclonal antibody was used for detecting antibody. Pooled plasma from healthy donors was used to plot the standard curve and the IgM concentration of pooled plasma was defined as 1. We set up an ELISA procedure to measure human IgM autoantibody to folate receptor. The sensitivity, precision, and stability of the method were evaluated. Further, the folate receptor and bovine folate-binding protein were used as the antigen, respectively, to determine the autoantibody levels in 24 healthy individuals and 20 individuals once gave birth to baby with neural tube defects. RESULTS: The measuring range of the method was from 6.25 × 10⁻4 to 8.00 × 10⁻². The lowest IgM level that can be detected was 3.12 × 10⁻4. The inter-assay coefficients of variations for samples with high, medium, and low IgM levels were 6.61%,3.50%, and 5.12%, respectively. The intra-assay coefficients of variations were 4.54%, 5.49%, and 5.44%, respectively. The stability test results were considered within acceptable limits. The data from folate receptor-ELISA was significantly higher than that from bovine folate binding protein-ELISA, both in the healthy group (t=-11.9, P<0.001) and in the neural tube defect group (t = 7.35, P<0.001). CONCLUSIONS: The folate receptor-ELISA method for measuring human IgM autoantibody to folate receptor was successfully established. The method is sensitive, repeatable, and stable.


Assuntos
Autoanticorpos/sangue , Ensaio de Imunoadsorção Enzimática/métodos , Receptor 2 de Folato/imunologia , Imunoglobulina M/sangue , Humanos
4.
Zhonghua Yu Fang Yi Xue Za Zhi ; 44(1): 70-4, 2010 Jan.
Artigo em Chinês | MEDLINE | ID: mdl-20388368

RESUMO

OBJECTIVE: To determine the association between pregnancy-induced hypertension(PIH) and risk of preterm delivery (PD) and low birth weight (LBW). METHODS: A prospective cohort was established based on 131 867 women who delivered a singleton baby in seven cities or counties in Zhejiang province, China, during the period of 1995 - 2000. The exposure group included 14 278 women who were diagnosed as PIH, and the non-exposure group included 117 589 women. The exposure group was divided into mild, moderate, and severe subgroups based on the severity of PIH, and further divided into early, medium and late onset subgroups based on the time of onset of PIH (occurred in second trimester, third trimester, or during delivery). The primary outcome measures were the incidence of PD and LBW. Multiple logistic regression was used to estimate relative risk and 95% confidence intervals after adjustment by maternal age, occupation, education, parity, number of prenatal visits, gestational disease, caesarean delivery, pregnant body mass index, fetal sex, and gestational age (only for LBW). RESULTS: The incidence rates of PD and LBW in exposure group were 4.9% (701/14 278) and 3.6% (507/14 278), and both rates were higher than those of the non-exposure group (3.4% (4031/117 589), 1.8% (2110/117 589)) (chi(2) values were 80.8 and 202.0, P < 0.001). The incidence rates of PD in mild, moderate, and severe subgroups were 3.9% (404/10 358), 5.8% (181/3099), and 14.1% (116/821), and corresponding incidence rates of LBW were 2.5% (258/10 358), 4.9% (151/3099), and 11.9% (98/821). Both rates were increased with the severity of PIH (chi(2) values were 196.4 and 426.1, P-value for trend < 0.001). The incidence rates of PD in early, medium, and late onset subgroup were 8.4% (50/598), 5.7% (278/4867), and 4.2% (373/8813), and corresponding incidence rates of LBW were 5.7% (34/598), 4.2% (206/4867), and 3.0% (267/8813). Both rates were decreased by the time of PIH onset (chi(2) values were 115.4 and 239.8, P-value for trend < 0.001). CONCLUSION: PIH could increase the incidence of PD and LBW.


Assuntos
Hipertensão Induzida pela Gravidez/epidemiologia , Recém-Nascido de Baixo Peso , Nascimento Prematuro , Adulto , Feminino , Humanos , Recém-Nascido , Gravidez , Estudos Prospectivos , Adulto Jovem
5.
Biol Trace Elem Res ; 198(2): 380-389, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32072446

RESUMO

Mercury (Hg), cadmium (Cd), and arsenic (As) concentrations in women were measured and compared to evaluate the effects of environmental heavy-metal pollution control on internal exposure levels. In 2005 and 2012, 200 and 182 women, respectively, were enrolled in the study. Demographic and diet information were collected using a questionnaire. Fasting venous blood samples were collected, and plasma concentrations of Hg, Cd, and As were measured using inductive coupled plasma mass spectrometry. The median concentrations (P25-P75) of Hg, Cd, and As decreased from 0.56 (0.46-0.75) ng/mL, 0.14 (0.09-0.21) ng/mL, and 0.83 (0.66-1.09) ng/mL in 2005 to 0.39 (0.19-0.66) ng/mL, 0.09 (0.05-0.13) ng/mL, and 0.48 (0.29-0.72) ng/mL in 2012, respectively. The difference in plasma metal concentrations between measurements in 2005 and 2012 remained statistically significant after we adjusted for confounders. The adjusted ORs were 0.31 (0.16-0.60), 0.24 (0.12-0.48), and 0.25 (0.13-0.50) for Hg, Cd, and As concentrations, respectively, in 2012, relative to those in 2005. The levels of Hg, Cd, and As were 30% to 40% lower in 2012 than in 2005, indicative of lower human internal exposure to these contaminants due to the implementation of environmental pollution control. Engagement with agriculture and high-frequency water product consumption were associated with high Hg levels, and a high frequency of consumption of fresh fruit and eggs was negatively associated with lower levels of Cd in plasma.


Assuntos
Arsênio , Mercúrio , Metais Pesados , Cádmio/análise , China , Feminino , Humanos , Mercúrio/análise , Metais Pesados/análise
6.
Zhonghua Yu Fang Yi Xue Za Zhi ; 40(6): 409-14, 2006 Nov.
Artigo em Chinês | MEDLINE | ID: mdl-17313741

RESUMO

OBJECTIVE: To study the association between transforming growth factor alpha gene (TGFalpha) TaqI variant and nonsyndromic cleft lip with or without cleft palate (nsCL/P) in Chinese population, and the interaction with parental smoking. METHODS: TGFalpha TaqI variant was detected using RFLP-PCR for DNA samples of the 170 triads with nsCL/P affected child. We performed the transmission/disequilibrium test (TDT) and the family-based association study (FBAT) to test the associations between this variant and risk of nsCL/P. RESULTS: It was not found significant distortion of C2 allele at TGFalpha TaqI locus in nsCL/P groups (P > 0.05), however, by stratified analysis, we found that the rate of C2 allele transmission among nuclear families whose fathers were smoking was 1/5 (0.062 - 0.711) as compared with that among nuclear families whose fathers were not smoking, and the OR of interaction between TGFalpha variant and parental smoking is 0.102 (0.017 - 0.619). CONCLUSION: The parental smoking may interact with TGFalpha variants of Chinese populations in occurrence of nsCL/P, but it remains to have more investigations.


Assuntos
Fenda Labial/epidemiologia , Fissura Palatina/epidemiologia , Fumar , Fator de Crescimento Transformador alfa/genética , Alelos , China/epidemiologia , Pai , Feminino , Frequência do Gene , Genótipo , Humanos , Recém-Nascido , Masculino , Mutação , Polimorfismo Genético , Gravidez , Fumar/efeitos adversos , Inquéritos e Questionários
7.
Wei Sheng Yan Jiu ; 35(2): 217-8, 2006 Mar.
Artigo em Chinês | MEDLINE | ID: mdl-16758976

RESUMO

OBJECTIVE: To understand the nitrate and nitrite contents of drinking water in Shanxi Province, China. METHODS: Water samples were collected from Pingding and Taigu counties and Taiyuan City. The nitrate and nitrite contents were determined following the 'Drinking water hygienic standard-2001'. RESULTS: The median nitrate content of drinking water was 3.5 mg/L, and the proportion of samples above national hygienic standard for drinking water was 4.0% in study areas. The median nitrite content of well water samples(5.l mg/L) was higher than that of tape water (2.7 mg/L). The median content of nitrite was 0.004 mg/L for all samples, and the median content of spring water was highest (0.017 mg/L) than that of other sources. Conclusion The contents of nitrate and nitrite in drinking water were similar to that reported form other regions. Maternal nitrate exposure from drinking water may not be among the important risk factors of high prevalence of birth defects in Shanxi Province.


Assuntos
Exposição Materna/efeitos adversos , Nitratos/análise , Nitritos/análise , Efeitos Tardios da Exposição Pré-Natal , Poluentes Químicos da Água/análise , China/epidemiologia , Feminino , Humanos , Masculino , Defeitos do Tubo Neural/induzido quimicamente , Defeitos do Tubo Neural/epidemiologia , Gravidez , Abastecimento de Água/análise
8.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 22(3): 284-7, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15952116

RESUMO

OBJECTIVE: To search the interaction between reduced folate carrier gene (RFC1 A80G) polymorphism of children with neural tube defects (NTDs) and maternal periconceptional no supplementation of folic acid. The purpose is to provide the epidemiological evidence for finding genetic marker of NTDs. METHODS: RFC1 (A80G) genotype was detected using PCR-restricted fragment length polymorphism for the blood DNA of 104 trios with NTDs-affected child, and 100 control families with non-malformed control children. The authors investigated the gene-environment interactions between the offspring RFC1 genotype and maternal periconceptional folic acid supplementation through a case-control study. RESULTS: It was observed that the offspring with the GG genotype were associated with a 2.56-fold increased risk of NTDs when compared to those with the AA genotype (OR = 2.56; 95% CI = 1.04-6.36) in this population under investigation. The risk of mothers who did not take folic acid for having an NTDs-affected infants was 7.69 (95% CI = 2.86-21.75). Among the mothers who did not utilize folic acid supplements, the NTDs risk was 3.30 (95% CI = 1.15-9.65) for offspring with the GG genotype, compared to the reference (AA) genotype. Children who had the GG genotype and whose mothers did not take folic acid had an elevated risk for NTDs (OR = 8.80, 95% CI = 2.86 - 29.82), compared to "offspring with AA or GA genotype" and "maternal folic acid use", the interactive coefficient being 1.45. CONCLUSION: The above findings indicate that the RFC1 genotype (GG) is a possible susceptible gene marker for an increased NTDs risk in Chinese population, and there is a potential gene-nutrient interaction between offspring RFC1 GG genotype and maternal periconceptional intake of folic acid on the risk of NTDs. However,the sample size of this study was limited, a larger sample of population-based study is required to pursue the initial observation.


Assuntos
Ácido Fólico/administração & dosagem , Proteínas de Membrana Transportadoras/genética , Defeitos do Tubo Neural/genética , Polimorfismo Genético/genética , Adulto , Estudos de Casos e Controles , Criança , Pré-Escolar , Suplementos Nutricionais , Feminino , Predisposição Genética para Doença/genética , Genótipo , Humanos , Masculino , Defeitos do Tubo Neural/prevenção & controle , Proteína Carregadora de Folato Reduzido , Complexo Vitamínico B/administração & dosagem
9.
Beijing Da Xue Xue Bao Yi Xue Ban ; 37(4): 341-5, 2005 Aug 18.
Artigo em Chinês | MEDLINE | ID: mdl-16086047

RESUMO

OBJECTIVE: To study the reduced folate carrier gene (RFC1) A80G polymorphism and other factors influence on children with neural tube defects (NTDs) and provide the epidemiological evidence for finding genetic marker of NTDs. METHODS: RFC1(A80G) genotypes were detected using polymerase chain reaction-restriction fragment length polymorphism (RFLP-PCR) for blood DNA of 104 trios with NTDs-affected by child, and the 100 control families without child-affected by any birth defects. We performed the analysis of multifactors logistic regression for RFC1 genotypes and other factors in order to investigate the RFC1 genotype of the nuclear families and maternal periconceptional folic acid supplementation influence on NTDs independently. Transmission/disequilibrium test (TDT) for the RFC1 genotype of NTDs and control pedigree were carried out. RESULTS: The RFC1 G allele frequency of children with NTDs (64.42%) was higher than that of the control children (52.53%), and there was the significant difference between them (chi(2)=5.9198, P<0.05). We observed that the infants of the GG genotype were associated with a 2.56-fold increased risk of NTDs when compared with the AA genotype (95% CI=1.04-6.36), The risk of mothers who did not take folic acid for having an NTDs-affected infants was 7.69 (95% CI=2.86-21.75). There were significant differences between cases and controls in the other risk factors, such as paternal age (> or =30), maternal fever during the early pregnancy, the history of maternal spontaneous abortion. In the logistic regression analysis, of multifactors the three factors, for example, the offspring of the RFC1 GG genotype (OR=2.91, 95% CI=1.35-6.30), maternal periconceptional folic acid supplementation (OR=4.32, 95% CI=1.62-11.55), maternal fever during the early pregnancy, had the statistic significance for the risk of NTDs. There was the evidence of an association between G allele and the risk of the maternal having a child with NTDs (OR=1.56, 95% CI=1.07-2.28) in TDT analysis. CONCLUSION: Our findings indicate that the RFC1 genotype (GG) is a possible susceptible gene marker for an increased NTDs risk in this Chinese population, and there is a potential influence on the risk of NTDs in maternal periconceptional folic acid supplementation, and maternal fever during the early pregnancy.


Assuntos
Deficiência de Ácido Fólico , Proteínas de Membrana Transportadoras/genética , Defeitos do Tubo Neural/genética , Polimorfismo Genético , Adulto , Criança , Pré-Escolar , China/epidemiologia , Saúde da Família , Feminino , Marcadores Genéticos , Genótipo , Humanos , Lactente , Modelos Logísticos , Masculino , Defeitos do Tubo Neural/epidemiologia , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Proteína Carregadora de Folato Reduzido , Fatores de Risco
10.
World J Clin Pediatr ; 4(3): 41-4, 2015 Aug 08.
Artigo em Inglês | MEDLINE | ID: mdl-26261765

RESUMO

Neural tube defects (NTDs) are a group of congenital malformations of the central nervous system that are caused by the closure failure of the embryonic neural tube by the 28(th) day of conception. Anencephaly and spina bifida are the two major subtypes. Fetuses with anencephaly are often stillborn or electively aborted due to prenatal diagnosis, or they die shortly after birth. Most infants with spina bifida are live-born and, with proper surgical treatment, can survive into adulthood. However, these children often have life-long physical disabilities. China has one of the highest prevalence of NTDs in the world. Inadequate dietary folate intake is believed to be the main cause of the cluster. Unlike many other countries that use staple fortification with folic acid as the public health strategy to prevent NTDs, the Chinese government provides all women who have a rural household registration and who plan to become pregnant with folic acid supplements, free of charge, through a nation-wide program started in 2009. Two to three years after the initiation of the program, the folic acid supplementation rate increased to 85% in the areas of the highest NTD prevalence. The mean plasma folate level of women during early and mid-pregnancy doubled the level before the program was introduced. However, most women began taking folic acid supplements when they knew that they were pregnant. This is too late for the protection of the embryonic neural tube. In a post-program survey of the women who reported folic acid supplementation, less than a quarter of the women began taking supplements prior to pregnancy, indicating that the remaining three quarters of the fetuses remained unprotected during the time of neural tube formation. Therefore, staple food fortification with folic acid should be considered as a priority in the prevention of NTDs.

11.
Zhonghua Liu Xing Bing Xue Za Zhi ; 34(8): 826-31, 2013 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-24423773

RESUMO

OBJECTIVE: To estimate the infertility rates and to examine factors that contribute to the variations in infertility rates among studies. METHODS: Wanfang, CQVIP, CNKI, and PubMed Database were searched for infertility relevant population-based prevalence studies between 1980 and 2012. Meta-analysis and meta-regression were used to calculate the pooled size of effect and to identify the sources of variation. RESULTS: A total of 27 articles using data from regional surveys were included in the review. Results showed that the combined prevalence was 5.7% (95% CI: 5.3%-6.1%). Combined prevalence rates of 1-year and 2-year infertility in newly married couples were 12.5% (95% CI: 9.5%-15.4%) and 6.6% (95% CI: 4.9%-8.4%), respectively, while were respectively 6.4% (95% CI: 4.2%-8.6%) and 3.0% (95% CI: 2.6%-3.3%), in women of reproductive age. Results from Meta-regression showed that the prevalence of 2-year infertility was lower than that of 1-year while infertility in regions was seen higher under the poor socioeconomic condition than in the better regions. Infertility in studies using cohort or prospective studies was seen to be higher than in other studies. CONCLUSION: Owing to the inconsistency in determining the numerator and denominator that were used to calculate the prevalence of infertility as well as the inconsistency in criteria used to define the infertility, an agreed definition on infertility needs to be followed, in order to facilitate the comparison among studies.


Assuntos
Medicina Baseada em Evidências , Infertilidade/epidemiologia , Adulto , China/epidemiologia , Feminino , Humanos , Masculino , Prevalência , Literatura de Revisão como Assunto
12.
Zhonghua Liu Xing Bing Xue Za Zhi ; 33(5): 509-12, 2012 May.
Artigo em Chinês | MEDLINE | ID: mdl-22883180

RESUMO

OBJECTIVE: To examine the impact of pregnancy termination before 28 weeks of gestation on the overall prevalence of neural tube defects (NTDs). METHODS: Data collected during the period of 2004 and 2010 from a birth defects surveillance system in Pingding county and Taigu county of Shanxi province were used. Number of births≥28 weeks of gestation and number of cases with major birth defects among the births were collected. Terminations of pregnancies before 28 weeks of gestation due to prenatal diagnosis were also collected. The total prevalence of neural tube defects, prevalence before 28 weeks of gestation, and prevalence of ≥28 weeks gestation were calculated using the total number of pregnancies of ≥28 weeks of gestation as denominator. The prevalence data were compared to examine the impact of pregnancy termination on the total prevalence. The proportions of pregnancy terminations before 28 weeks of gestation due to prenatal diagnosis of an NTD against the total number of NTD cases were also calculated. RESULTS: During 2004-2010, 52 366 births were recorded, and 485 NTD cases were ascertained. The overall prevalence of NTDs was 92.6 per 10,000 births, with prevalence of <28 weeks gestation due to pregnancy terminations as 60.9 per 10,000 births, while the prevalence of ≥28 weeks of gestation was 31.7 per 10,000 births. NTD prevalence of ≥28 weeks gestation was 66.0% lower than the total NTD prevalence. In the last two years, the proportion of NTDs ascertained ≥28 weeks gestation accounted for about 40.0% of the total NTD cases. CONCLUSION: A birth-defect-surveillance program that covered only pregnancies≥28 weeks of gestation resulted in a severe underestimation of the total birth prevalence of NTDs, especially for anencephaly. We would recommend that the current national birth defects surveillance system should include pregnancy terminations before 28 weeks of gestation and the calculation of total NTD prevalence should also include these cases into the numerator, so as to better estimate true population NTD prevalence, upon which the related public health policy is based.


Assuntos
Aborto Induzido/estatística & dados numéricos , Defeitos do Tubo Neural/epidemiologia , China/epidemiologia , Feminino , Humanos , Gravidez , Prevalência
13.
Chin Med J (Engl) ; 124(11): 1629-33, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21740767

RESUMO

BACKGROUND: Maternal exposure to nitrate, nitrite, and N-nitroso compounds from drinking water or diet has been associated with an increased risk of neural tube defects (NTDs) in some studies. Pickled vegetables contain relatively large amounts of nitrite and N-nitroso compounds. We examined the association between maternal periconceptional consumption of pickled vegetables and NTDs in Shanxi Province of northern China. METHODS: Data were derived from a population based case-control study of major external birth defects in four counties of Shanxi Province. Participants included 519 NTDs cases identified between 2003 and 2007 and 694 healthy controls. Exposure information was collected within 1 week after delivery. Multivariable non-conditional Logistic regression model was used to estimate the adjusted odds ratio (OR) controlling for potential confounding variables. RESULTS: The risk of NTDs was positively associated with the frequency of the consumption of pickled vegetables by the mother. Compared with pickled vegetables consumption at < 1 meal/week, the adjusted OR for consumption at 1 - 3, 4 - 6, and > 6 meals/week were 1.3 (95% confidence interval (CI): 1.0, 1.8), 1.9 (1.1, 3.2), and 3.6 (1.9, 6.9), respectively. A protective effect was found for maternal meat consumption at ≥ 1 meal/week (adjusted OR: 0.6, 95%CI: 0.4, 0.7) and egg or milk consumption at ≥ 1 meal/week (adjusted OR: 0.6, 95%CI: 0.4, 0.8). CONCLUSION: Maternal periconceptional consumption of pickled vegetables may increase the risk for NTDs in Shanxi Province.


Assuntos
Exposição Materna/efeitos adversos , Defeitos do Tubo Neural/etiologia , Verduras/efeitos adversos , Verduras/química , Adulto , Estudos de Casos e Controles , Feminino , Humanos , Recém-Nascido , Modelos Logísticos , Análise Multivariada , Nitritos/efeitos adversos , Compostos Nitrosos/efeitos adversos , Gravidez , Fatores de Risco , Adulto Jovem
14.
Chin Med J (Engl) ; 124(23): 3982-7, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22340328

RESUMO

BACKGROUND: Cesarean section births have been steadily increasing over the past decade and have become an epidemic in China. Cesarean delivery on maternal request is a major contributor to this upward trend, and there has been of much concern about its impact on maternal and child health. Most of mothers believe that cesarean delivery on maternal request can improve the child's intelligence, but direct evidence is sparse. In this cohort study, we aimed to directly assess the impact of cesarean delivery on maternal request on childhood intelligence. METHODS: Intelligence quotient (IQ) of 4144 preschool children from 21 cities/counties of Zhejiang and Jiangsu province whose mothers were registered in a population-based perinatal surveillance program during 1993-1996 was assessed with Chinese Wechsler Young Children Scale of Intelligence (C-WYCSI) in 2000. The outcomes were full-scale IQ, verbal IQ, and performance IQ of C-WYCSI. Mode of delivery and covariates were obtained from the surveillance program. We estimated unadjusted and adjusted effects of cesarean delivery on maternal request and assisted vaginal delivery on IQ scores compared with spontaneous vaginal delivery using regression analysis. RESULTS: The mean full-scale, verbal, and performance IQ for all children was 99.3 ± 16.1, 93.6 ± 17.7, and 105.3 ± 14.3. In crude analysis, cesarean delivery on maternal request versus spontaneous vaginal delivery was associated with an increase of 3.9 (95% confidence interval, 0.6 to 7.2) points in full-scale IQ, 4.8 (1.2 to 8.4) points in verbal IQ, and 2.4 (-0.6 to 5.3) points in performance IQ. After adjusting for maternal education, occupation, and IQ, the advantage was reduced to 1.6 (-1.3 to 4.5), 2.3 (-0.8 to 5.5), and 0.6 (-2.0 to 3.3) points for full-scale, verbal, and performance IQ, respectively. Assisted vaginal delivery versus spontaneous vaginal delivery was not associated with IQ scores in any analysis. CONCLUSION: Neither cesarean delivery on maternal request nor assisted vaginal delivery affected children's IQ.


Assuntos
Cesárea/efeitos adversos , Inteligência/fisiologia , Criança , Pré-Escolar , Feminino , Humanos , Testes de Inteligência , Masculino , Gravidez
15.
Zhonghua Liu Xing Bing Xue Za Zhi ; 31(2): 223-6, 2010 Feb.
Artigo em Chinês | MEDLINE | ID: mdl-21215089

RESUMO

In this article, we presented the rationale and calculation procedures of a propensity score weighting method, with its application in epidemiological studies. The rationale for propensity score weighting method is similar to those for traditional standardization methods. Propensity score is used to estimate the weight for each individual. As the propensity score serves the function of observed covariates, the propensity score weighting can balance the distribution of the observed covariates between the comparison groups. There are two weighting methods according to the target standard populations: the Inverse probability of treatment weighting (IPTW) and the Standardized mortality ratio weighting (SMRW). Results of the example show that the distribution of the covariates tended to be consistent after weighting, and the IPTW and SMRW methods showed similar effect estimates. Propensity score weighting method can effectively balance the distribution of the confounding factors between the compared groups in non-randomized controlled trials.


Assuntos
Pontuação de Propensão , Demografia , Feminino , Humanos , Hipertensão Induzida pela Gravidez/prevenção & controle , Modelos Estatísticos , Padrões de Referência
16.
Zhonghua Liu Xing Bing Xue Za Zhi ; 31(11): 1259-63, 2010 Nov.
Artigo em Chinês | MEDLINE | ID: mdl-21176688

RESUMO

OBJECTIVE: To understand the extent and relative changes of equities in using the prenatal care services among premature delivery women from 4 counties/cities in Jiangsu and Zhejiang provinces, from 1995 to 2000. METHODS: The study population consisted of 97 537 women who delivered singleton live birth of 28 to 41 gestational weeks in 4 counties/cities of Jiangsu and Zhejiang provinces, from 1995 to 2000. The proportions of women with early prenatal visit, of those with at least five prenatal visits and the hospital delivery rates between premature and term delivery groups were calculated. Inequalities in the above indictors by comparing rate difference (RD), rate ratio (RR) and concentration index (CI) among women with different educational levels, were examined. Chi-square and One-way ANOVA were used to compare the differences. RESULTS: The proportions of having received early prenatal among those women with premature delivery in different education levels were 82.89%, 91.06%, 93.96%, 93.11% respectively, which were less than that of those with full term delivery (86.36%, 93.95%, 95.65%, 96.41%, P = 0.008). The proportions of having received early prenatal among the women with high educational levels were higher (RD = -10.05, RR = 0.90, CI = 0.0104) than those with low educational attainment (RD = -10.22, RR = 0.89, CI = 0.0131); The proportions of having received at least five prenatal visits among those women with premature delivery in different education levels were 86.54%, 93.17%, 92.99%, 96.49%, respectively, which were less than those with full term delivery (94.60%, 96.65%, 96.15%, 96.66%, P = 0.005). The proportions of having had at least five prenatal visits among the women with high educational attainment were higher (RD = -2.06, RR = 0.98, CI = 0.0006) than those with lower educational attainment (RD = -9.95, RR = 0.90, CI = 0.0077); The proportions of hospital delivery among the women with full term delivery in different education levels were significantly higher (99.45%, 99.75%, 99.83%, 99.77%) than those with premature deliveries (98.42%, 99.54%, 99.61%, 100.00%, P = 0.005). The proportions of hospital delivery among women with high educational attainment was higher (RD = -0.32, CI = 0.0003) than those with lower educational attainment (RD = -1.58, CI = 0.0013). CONCLUSION: Education related inequities in prenatal care utilization had not been improved among the Chinese women under our study. Inequities were seen in those women with full-term delivery the preterm delivery ones.


Assuntos
Nascimento Prematuro , Cuidado Pré-Natal , Feminino , Humanos , Fatores Socioeconômicos
17.
Zhonghua Liu Xing Bing Xue Za Zhi ; 31(12): 1353-8, 2010 Dec.
Artigo em Chinês | MEDLINE | ID: mdl-21223663

RESUMO

OBJECTIVE: The purpose of this study was to evaluate the effect of hemoglobin (Hb) level during early gestation on the cognitive development of children at 4 - 6 years of age. METHODS: A total number of 3609 children were randomly selected from all the live birth infants whose mothers participated in a community intervention trial during 1993 - 1996 in 13 counties or cities in Jiangsu and Zhejiang provinces. Hb concentration during early gestation was measured at first prenatal examination and intelligence quotients (IQ), including full-scale, verbal and performance were assessed using Chinese-Wechsler Intelligence Scale for Children in 2000 - 2001 when these children had a mean age of 68 months. RESULTS: Compared with children whose mothers were non-anemic during early gestation, children whose mothers were anemic had a 0.6 point higher mean verbal scale IQ, a 0.9 point higher mean performance IQ and a 0.8 point higher mean full-scale IQ. These differences were not statistically significant when children's gender, age at intelligence test, region, parity and mother's IQ, education level and occupation were adjusted for. When mother-child pairs were divided into 5 sub-groups of every 20 percentiles according to Hb concentration during early gestation, verbal IQ scores of the lowest (Hb < 103 g/L), the moderate (110 g/L ≤ Hb < 116 g/L) and the highest Hb concentration group (Hb ≥ 124 g/L) were 91.6 ± 18.9, 92.8 ± 18.2 and 90.3 ± 18.6, respectively. The performance IQ scores were 104.7 ± 15.2, 104.5 ± 14.3 and 103.5 ± 15.1, and full-scale IQ scores were 97.8 ± 17.3, 98.4 ± 16.3 and 96.4 ± 17.4, respectively. After controlling for confounding factors, children whose mothers had highest Hb concentration were 54% (OR = 1.54, 95%CI: 1.13 - 2.11) more likely to have poor verbal scores and 53% (OR = 1.53, 95%CI: 1.10 - 2.12) more likely to have poor full-scale scores than children whose mothers had moderate Hb concentration. No statistical associations were noticed between high Hb concentration and performance scores, or between low Hb concentration during early gestation and verbal, performance as well as full-scale score of pre-school children. CONCLUSION: High maternal Hb concentration during early gestation might adversely affect children's cognitive development.


Assuntos
Desenvolvimento Infantil , Hemoglobinas/metabolismo , Inteligência , Adulto , Pré-Escolar , Feminino , Humanos , Testes de Inteligência , Masculino , Gravidez , Primeiro Trimestre da Gravidez , Adulto Jovem
18.
Zhonghua Liu Xing Bing Xue Za Zhi ; 31(4): 389-93, 2010 Apr.
Artigo em Chinês | MEDLINE | ID: mdl-20513281

RESUMO

OBJECTIVE: Our purpose was to evaluate the association between hemoglobin concentration (Hb) and cognitive ability of children at 4 - 6 years of age in 21 counties/cities in China. METHODS: A total number of 7331 children born during 1993 - 1996 were randomly selected from 21 counties or cities in Hebei, Jiangsu and Zhejiang provinces. Hb concentration of children were measured followed by three tests including full-scale, verbal and performance intelligence quotient (IQ) test performed by Chinese-Wechsler Intelligence Scale for Children, one year later. RESULTS: There were a 0.7 point difference in mean verbal scale IQ (P = 0.144) and a 0.9 point difference in both mean performance and full-scale IQ (P = 0.055 and 0.079, respectively) between anemia and non-anemia groups. Compared with children with non-anemia, children with anemia were 1.3-fold more likely to score poorly in verbal IQ and operational IQ (95%CI: 1.1 - 1.6, 1.1 - 1.5, respectively) and 1.4-fold more likely to have had poor scores in full-scale IQ (95%CI: 1.2 - 1.6) after controlled for children's gender, age at intelligence test, region, parity and mother's IQ, education level, occupation. Participants were divided into 5 sub-groups according to Hb concentration of every 20 percentile. Verbal IQ scores of the lowest (Hb < 110 g/L), moderate (117 g/L /= 130 g/L) were 90.6 +/- 18.1, 94.0 +/- 17.6 and 91.0 +/- 16.4, respectively. Performance IQ scores were 102.2 +/- 15.7, 104.6 +/- 14.8 and 100.5 +/- 14.9, respectively. Full-scale IQ scores were 95.9 +/- 17.3, 99.0 +/- 16.4 and 95.2 +/- 15.6, respectively. Children with both low and high hemoglobin levels did poorly in all intelligence tests than children with moderate Hb concentration (P < 0.001). After controlling for confounding factors, children with the lowest concentration were 1.4-fold more likely to have had poor verbal and performance scores than children with moderate Hb concentration (95%CI: 1.1 - 1.7, 1.1 - 1.8, respectively) and 1.5-fold (95%CI: 1.2 - 1.8) more likely to have had poor full-scale scores than those with moderate Hb concentration. The association between high Hb concentration and low IQ scores disappeared in the multivariate model. CONCLUSION: Low Hb concentration might have adversely affected children's cognitive development.


Assuntos
Desenvolvimento Infantil , Hemoglobinas/análise , Inteligência , Anemia/epidemiologia , Pré-Escolar , Feminino , Humanos , Testes de Inteligência , Masculino
19.
Zhonghua Liu Xing Bing Xue Za Zhi ; 31(7): 755-8, 2010 Jul.
Artigo em Chinês | MEDLINE | ID: mdl-21162837

RESUMO

OBJECTIVE: To study the current status of spontaneous abortion of primigravid women in Jiaxing areas of Zhejiang province of China. METHODS: We analyzed the data from both perinatal healthcare surveillance program and spontaneous abortion, collected in Jiaxing areas by the Institute of Reproductive and Child Health, Peking University. The study population consisted of 14 769 primigravid women (excluding induced abortion, ectopic pregnancy and molar pregnancy as outcomes) attempting to become pregnant who registered between 1993 and 1995. RESULTS: 1454 spontaneous abortion cases were identified, with the spontaneous abortion rate as 9.8% (95%CI: 9.3% - 10.3%). The mean gestational weeks at pregnancy diagnosis were 7.6 ± 2.1 weeks, the mean gestational weeks at miscarriage were (10.1 ± 3.1) weeks and the incidence of first-trimester (≤ 12 weeks) spontaneous abortion was 7.3% (95%CI: 6.8% - 7.7%), accounting for 73.7% of all the spontaneous abortion cases. A peak for risk of miscarriage was around 8 - 13 weeks, accounting for 37.7% of all spontaneous abortion. The observed multiple Cox regression model showed that increased spontaneous abortion rates were observed in women with age at pregnancy ≥ 30, being peasants and with higher education level. CONCLUSION: The spontaneous abortion rate of primigravid women in Jiaxing areas was higher than in other areas of China. The maximum occurrence of spontaneous abortions was during period of 8-13 gestation weeks.


Assuntos
Aborto Espontâneo/epidemiologia , Adulto , China/epidemiologia , Feminino , Número de Gestações , Humanos , Gravidez , Fatores de Risco
20.
Zhonghua Liu Xing Bing Xue Za Zhi ; 31(5): 506-9, 2010 May.
Artigo em Chinês | MEDLINE | ID: mdl-21163025

RESUMO

OBJECTIVE: To analyze the influencing factors for stunting and underweight among children aged 3 - 6 years in 15 counties of Jiangsu and Zhejiang provinces so as to provide reference for enhancing growth level among preschool children. METHODS: Data was from the 183 295 records of Children Follow-up Study Project carried out by the Institute of Reproductive and Child Heath of Peking University and the records of related perinatal health care surveillance system in rural areas of 15 counties/cities of Jiangsu and Zhejiang provinces. WHO-NCHS standard was used to assess the childhood physical level of growth. Data of children's birth and their mothers' perinatal health were correlated to determine influencing factors for childhood stunting and underweight. RESULTS: The average stunting rate was 7.95% and underweight rate was 1.55%. Sex, birth weight, preterm birth as well as maternal height, maternal BMI at the first prenatal visit, maternal education and occupation were significantly related to childhood stunting and underweight. Birth weight was the most important influencing factor for childhood underweight. For the groups whose birth weights were < 2500 g and ≥ 2500 g, the rates of underweight were 7.77% and 1.46% respectively. Children with low birth weight were at higher risk for underweight (OR = 3.68, 95%CI: 3.11 - 4.37). Maternal height was the most important influencing factor for childhood stunting. For the groups whose mothers' heights were < 155 cm, 155 - 160 cm, 160 - 165 cm and ≥ 165 cm, the stunting rates were 13.01%, 8.76%, 6.21% and 4.14% respectively. Compared with the ≥ 165 cm group, the < 155 cm group was at higher risk for stunting (OR = 3.08, 95%CI: 2.82 - 3.37). CONCLUSION: Birth weight and maternal height were key factors influencing the growth of children. Perinatal health care and the nutrition status of pregnant mothers should be improved to promote the growth level of preschool children.


Assuntos
Desenvolvimento Infantil , Somatotipos , Magreza/epidemiologia , Peso ao Nascer , Criança , Pré-Escolar , China/epidemiologia , Feminino , Humanos , Masculino , Mães , Estado Nutricional , Gravidez
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