Objective To reconfirm the association of KPNB3 with schizophrenia in Chinese population. Methods Two single nucleotide polymorphisms (SNPs), rs2588014 and rs626716 trios consisting of fathers, mothers, and affected...Objective To reconfirm the association of KPNB3 with schizophrenia in Chinese population. Methods Two single nucleotide polymorphisms (SNPs), rs2588014 and rs626716 trios consisting of fathers, mothers, and affected offsprings at the KPNB3 locus, were genotyped in 304 Chinese Han family with schizophrenia. These 2 SNPs were detected by PCR-based restriction fragment length polymorphism (RFLP) analysis. The Hardy-Weinberg equilibrium for genotypic distributions was estimated by the goodness-of-fit test. The UNPHASED program was used to perform transmission disequilibrium test (TDT), haplotype analysis, and pair-wise measure of linkage disequilibrium (LD) between these 2 SNPs. Results The genotypic distributions of both rs2588014 and rs626716 were in the Hardy-Weinberg equilibrium (P〉0.05). The TDT revealed allelic association with rs626716 (χ^2 =9.31, P=0.0023) but not with rs2588014 (χ^2 =3.44, P=0.064). The global P-value was 0.0099 for 100 permutations. The haplotype analysis also showed a disease association (χ^2 =25.97, df=3, P=0.0000097). Conclusion The present study provides further evidence in support of the KPNB3 association with schizophrenia in Chinese population.展开更多
Abnormal phospholipid metabolism in the brain plays an important role in neuropsychiatric diseases.Phospholipase A2(PLA2)is a crucial element for normal neuro-physiological function.This study aims to investi-gate the...Abnormal phospholipid metabolism in the brain plays an important role in neuropsychiatric diseases.Phospholipase A2(PLA2)is a crucial element for normal neuro-physiological function.This study aims to investi-gate the genetic association between the polymorphism of cytosolic phospholipase A2(cPLA2)family genes and schizophrenia among Han Chinese in the northern part of China.The polymerase chain reaction-based ligase detec-tion reaction(PCR-LDR)was applied to detect the genotype ten single nucleotide polymorphisms(SNPs)of cPLA2 family genes among 201 pedigrees consisting of fathers,mothers and affected offsprings with schizophre-nia.The pedigrees were collected from 2000 to 2006.Haplotype relative risk(HRR)test,transmission disequili-brium test(TDT),haplotype transmission analysis and multiple locus analysis were conducted to analyze the genotyping data.The genotypic frequency of cPLA2 gene did not deviate from Hardy-Weinberg equilibrium either in case or control group.HRR and TDT showed that the ten SNPs were not associated with schizophrenia(P>0.05).Analysis for haplotype transmission showed that no haplotype system was associated with schizophrenia(P>0.05).The conditioning on allele(COA)and conditioning on gene(COG)tests showed disease associations with the haplotype of rs2162886-rs1668589,rs891014-rs1668589 and rs2307279-rs7542180(χ2=6.913,P=0.032;χ2=8.393,P=0.015;χ2=8.447,P=0.038).Our data suggest that many loci in the cPLA2 family genes may be associated with schizophrenia.展开更多
基金This work was supported by the National 863 Program (No. 2001AA221072 and 2004AA221070)the National Key Technology Research and Development Program of China (No. 2002BA711A07)+1 种基金the National Natural Science Foundation of China (No. 39970165 and 30400263)the Beijing Natural Science Foundation (No. 5052021).
文摘Objective To reconfirm the association of KPNB3 with schizophrenia in Chinese population. Methods Two single nucleotide polymorphisms (SNPs), rs2588014 and rs626716 trios consisting of fathers, mothers, and affected offsprings at the KPNB3 locus, were genotyped in 304 Chinese Han family with schizophrenia. These 2 SNPs were detected by PCR-based restriction fragment length polymorphism (RFLP) analysis. The Hardy-Weinberg equilibrium for genotypic distributions was estimated by the goodness-of-fit test. The UNPHASED program was used to perform transmission disequilibrium test (TDT), haplotype analysis, and pair-wise measure of linkage disequilibrium (LD) between these 2 SNPs. Results The genotypic distributions of both rs2588014 and rs626716 were in the Hardy-Weinberg equilibrium (P〉0.05). The TDT revealed allelic association with rs626716 (χ^2 =9.31, P=0.0023) but not with rs2588014 (χ^2 =3.44, P=0.064). The global P-value was 0.0099 for 100 permutations. The haplotype analysis also showed a disease association (χ^2 =25.97, df=3, P=0.0000097). Conclusion The present study provides further evidence in support of the KPNB3 association with schizophrenia in Chinese population.
文摘Abnormal phospholipid metabolism in the brain plays an important role in neuropsychiatric diseases.Phospholipase A2(PLA2)is a crucial element for normal neuro-physiological function.This study aims to investi-gate the genetic association between the polymorphism of cytosolic phospholipase A2(cPLA2)family genes and schizophrenia among Han Chinese in the northern part of China.The polymerase chain reaction-based ligase detec-tion reaction(PCR-LDR)was applied to detect the genotype ten single nucleotide polymorphisms(SNPs)of cPLA2 family genes among 201 pedigrees consisting of fathers,mothers and affected offsprings with schizophre-nia.The pedigrees were collected from 2000 to 2006.Haplotype relative risk(HRR)test,transmission disequili-brium test(TDT),haplotype transmission analysis and multiple locus analysis were conducted to analyze the genotyping data.The genotypic frequency of cPLA2 gene did not deviate from Hardy-Weinberg equilibrium either in case or control group.HRR and TDT showed that the ten SNPs were not associated with schizophrenia(P>0.05).Analysis for haplotype transmission showed that no haplotype system was associated with schizophrenia(P>0.05).The conditioning on allele(COA)and conditioning on gene(COG)tests showed disease associations with the haplotype of rs2162886-rs1668589,rs891014-rs1668589 and rs2307279-rs7542180(χ2=6.913,P=0.032;χ2=8.393,P=0.015;χ2=8.447,P=0.038).Our data suggest that many loci in the cPLA2 family genes may be associated with schizophrenia.