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1.
Chinese Journal of Epidemiology ; (12): 74-78, 2020.
Article in Chinese | WPRIM | ID: wpr-787705

ABSTRACT

To investigate the relationship between exposure to famine in fetus and infant period and the risks for hypertension in adulthood. A total of 5 960 participants born between 1956 and 1965 were included in the study and were divided into unexposed group (1963-1965), fetal exposed group (1959-1961), early- childhood exposed group (1956-1958) and transitional group (1962). Logistic regression model was used to explore the association between famine exposure in early life and the risk for hypertension in adulthood. Both the fetal exposure and the early-childhood exposure were the risk factors for hypertension in adulthood (=1.249, 95: 1.049-1.486 and =1.360, 95: 1.102-1.679). Meanwhile, in rural area, compared with unexposed group, the fetal exposure (=1.401, 95: 1.091-1.798) and the early-childhood exposure (=1.460, 95: 1.145-1.862) were also associated with a greater risk of hypertension in adulthood. In addition, fetal exposure and early-childhood exposure to famine in women were associated with 36.0 and 31.9 increased risks for hypertension (95: 7.8-71.7 and 95: 4.8-66.0) according to the stratified analysis. Fetal exposure to famine might increase the risk for hypertension in adulthood.

2.
Biomedical and Environmental Sciences ; (12): 534-538, 2016.
Article in English | WPRIM | ID: wpr-296571

ABSTRACT

Dyslipidemia is a risk factor for cardiovascular diseases (CVDs) in patients with diabetes, and non-high-density lipoprotein cholesterol (non-HDL-C) is a better predictor of CVDs than low-density lipoprotein cholesterol (LDL-C) in patients with diabetes. Therefore, we aimed to investigate the distribution of non-HDL-C and the prevalence of high non-HDL-C level in Chinese patients with diabetes mellitus and identify the associated risk factors. Non-HDL-C concentration positively correlated with total cholesterol, triglycerides, and LDL-C concentrations. Although both non-HDL-C and LDL-C concentration both related positively with TC concentration, the magnitude of correlation was relatively higher for non-HDL-C. The prevalence of high non-HDL-C (⋝4.14 mmol/L) was higher in two age groups (55-64 years: 46.7%; 65-79 years: 47.3%) than other age groups (18-24 years: 4.2%; 25-34 years: 43.6%; 35-44 years: 38.1%; 45-54 years: 41.0%). It was also higher among overweight (45.1%), generally obese (50.9%), or abdominally obese (47.3%) subjects, compared with normal weight subjects (34.5%). The risk of high non-HDL-C increased with advancing age. Both general obesity [odds ratio (OR)=1.488, 95% confidence interval (CI): 1.003-2.209] and abdominal obesity (OR=1.561, 95% CI: 1.101-2.214) were significantly associated with high non-HDL-C levels.


Subject(s)
Adolescent , Adult , Female , Humans , Male , Middle Aged , Young Adult , China , Epidemiology , Cross-Sectional Studies , Diabetes Mellitus , Epidemiology , Hypercholesterolemia , Epidemiology , Prevalence , Risk Factors
3.
Chinese Journal of Epidemiology ; (12): 1265-1268, 2009.
Article in Chinese | WPRIM | ID: wpr-321073

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the genetic association between brain-derived neurotrophic factor (BDNF) gene polymorphism and internalizing disorders, to provide the theoretical basis to explore the etiology of internalizing disorders.</p><p><b>METHODS</b>PCR-based ligase detection reaction (PCR-LDR) was applied to tag single nucleotide lengh polymorphism (SNPs) of BDNF gene among 259 undergraduates affected by internalizing disorders and 269 healthy undergraduates. Haplotype analysis and multiple locus analysis were conducted to analyze the genotyping data.</p><p><b>RESULTS</b>The genotypic frequency of tag SNPs of BDNF gene did not deviate from Hardy-Weinberg equilibrium in both case and control groups. Rs12273539 was not associated with internalizing disorders (P > 0.05), but rs10835210 and rs2030324 were related to internalizing disorders (P < 0.05). The case group had more A allele of rs10835210 and C allele of rs2030324 when compared to the controls while A allele of rs10835210 and C allele of rs2030324 seemed to be the risk factors of internalizing disorder (OR = 1.877, P < 0.001; OR = 1.347, P < 0.05). Results of multiple locus analysis showed that the haplotype composed by the three tag SNPs which was related to internalizing disorders (chi(2) = 23.537, P < 0.001).</p><p><b>CONCLUSION</b>BDNF gene might serve as the susceptible gene for internalizing disorder.</p>


Subject(s)
Adult , Female , Humans , Male , Young Adult , Alleles , Brain-Derived Neurotrophic Factor , Genetics , Case-Control Studies , Gene Frequency , Genetic Predisposition to Disease , Genotype , Haplotypes , Mental Disorders , Genetics , Polymorphism, Single Nucleotide , Risk Factors
4.
Chinese Journal of Epidemiology ; (12): 173-176, 2008.
Article in Chinese | WPRIM | ID: wpr-287846

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the genetic association between the polymorphism of cytosolic phospholipase A2 (cPLA2) family genes and schizophrenia in the North Han Chinese.</p><p><b>METHODS</b>Method of polymerase chain reaction-based ligase detection reaction (PCR-LDR) was applied to genotype 10 single nucleotide polymorphisms (SNPs) of cPLA2 family genes among 201 pedigrees consisting of fathers, mothers and affected offsprings with schizophrenia. Haplotype relative risk (HRR) test, transmission disequilibrium test (TDT), haplotype transmission analysis and multiple locus analysis were conducted to analyze the genotyping data.</p><p><b>RESULTS</b>The genotypic frequency of cPLA2 gene did not deviate from Hardy-Weinberg equilibrium in both case and control groups. HRR and TDT showed that the 10 SNPs were not associated with schizophrenia (P > 0.05). Analysis for haplotype transmission showed that no haplotype systems was associated with schizophrenia (P > 0.05). Results from COA and COG tests showed a disease association for the rs2162886-rs1668589, rs891014-rs1668589 and rs2307279-rs7542180 combinations (chi2 = 6.913, P = 0.032; chi2 = 8.393, P = 0.015; chi2 = 8.447, P = 0.038).</p><p><b>CONCLUSION</b>Many loci in the cPLA2 family genes were associated with schizophrenic.</p>


Subject(s)
Adolescent , Adult , Female , Humans , Male , Young Adult , Asian People , Genetics , China , Epidemiology , Gene Frequency , Genetics , Genetic Predisposition to Disease , Genetics , Genotype , Haplotypes , Genetics , Phospholipases A2, Cytosolic , Genetics , Polymorphism, Single Nucleotide , Genetics , Schizophrenia , Epidemiology , Genetics
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