Matches in SemOpenAlex for { <https://semopenalex.org/work/W1529881836> ?p ?o ?g. }
- W1529881836 endingPage "575" @default.
- W1529881836 startingPage "569" @default.
- W1529881836 abstract "Genetic polymorphisms in apolipoprotein genes may be associated with alteration in lipid profile and susceptibility to gallstone disease.To determine the association between apolipoprotein A1 (APOA1) -75 guanine [G] to adenine [A] and +83/84 M2(+/-), MspI) and apolipoprotein C3 (APOC3) (SstI) polymorphisms with gallstone disease.MspI polymorphisms of the APOA1 gene and SstI polymorphisms of APOC3 were analyzed in DNA samples of 214 gallstone patients and 322 age- and sex-matched healthy controls. All statistical analyses were performed using SPSS version 11.5 (SPSS, USA) and Arlequin version 2.0 (Arlequin, Switzerland).The APOA1 -75 G/A polymorphism was significantly associated with gallstone disease. Patients with the GG genotype (P=0.015) and G allele carriers (P=0.004) had a significantly higher risk of gallstone disease (1.087-fold and 1.561-fold, respectively), whereas patients with AA genotypes (P=0.011) and A allele carriers (P=0.004) were protected (OR 0.230 and 0.641, respectively) against gallstone disease. APOA1 +83 M2(+/-) and APOC3 SstI polymorphisms were not associated with gallstone disease. Case-control analysis of haplotypes showed a significant association in males only. G-M2(+)-S1 conferred risk for gallstone disease (P=0.036; OR 1.593, 95% CI 1.029 to 2.464), while A-M2(+)-S1 was protective (P=0.002; OR 0.370, 95% CI 0.197 to 0.695) against gallstone disease. In APOA1(-75)-APOA1(+83) bilocus haplotypes, G-M2(+) was associated (P=0.0001) with very high risk (OR 3.173, 95% CI 1.774 to 5.674) for gallstone disease in males only. APOA1(-75)-APOC3(SstI) haplotypes also showed significant association while APOA1(+83)-APOC3(SstI) haplotypes showed no association with gallstone disease.The APOA1 -75 G/A polymorphism is associated with gallstone disease and shows sex-specific differences. On the other hand, APOA1 M2(+/-) and APOC3 SstI polymorphisms may not be associated with gallstone disease. Haplotype analysis is a better predictor of risk for gallstone disease." @default.
- W1529881836 created "2016-06-24" @default.
- W1529881836 creator A5036843120 @default.
- W1529881836 creator A5040504384 @default.
- W1529881836 creator A5045441660 @default.
- W1529881836 creator A5069458671 @default.
- W1529881836 date "2007-01-01" @default.
- W1529881836 modified "2023-10-12" @default.
- W1529881836 title "Association of<i>Apolipoprotein A1-C3</i>Gene Cluster Polymorphisms with Gallstone Disease" @default.
- W1529881836 cites W1545109971 @default.
- W1529881836 cites W1572007132 @default.
- W1529881836 cites W1844912259 @default.
- W1529881836 cites W1883778420 @default.
- W1529881836 cites W1942705224 @default.
- W1529881836 cites W1972808915 @default.
- W1529881836 cites W1988894404 @default.
- W1529881836 cites W2007835979 @default.
- W1529881836 cites W2007918998 @default.
- W1529881836 cites W2035137682 @default.
- W1529881836 cites W2046868406 @default.
- W1529881836 cites W2049461047 @default.
- W1529881836 cites W2059589608 @default.
- W1529881836 cites W2061014327 @default.
- W1529881836 cites W2062191156 @default.
- W1529881836 cites W2068689577 @default.
- W1529881836 cites W2068797485 @default.
- W1529881836 cites W2069594320 @default.
- W1529881836 cites W2075324589 @default.
- W1529881836 cites W2083673779 @default.
- W1529881836 cites W2088615805 @default.
- W1529881836 cites W2101452887 @default.
- W1529881836 cites W2110785249 @default.
- W1529881836 cites W2113999752 @default.
- W1529881836 cites W2118094114 @default.
- W1529881836 cites W2120757011 @default.
- W1529881836 cites W2126989486 @default.
- W1529881836 cites W2135922747 @default.
- W1529881836 cites W2137716547 @default.
- W1529881836 cites W2166233569 @default.
- W1529881836 cites W2269534525 @default.
- W1529881836 cites W2345501463 @default.
- W1529881836 cites W2413531016 @default.
- W1529881836 cites W2465455114 @default.
- W1529881836 cites W64668228 @default.
- W1529881836 cites W2357666427 @default.
- W1529881836 doi "https://doi.org/10.1155/2007/329342" @default.
- W1529881836 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2657985" @default.
- W1529881836 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17853951" @default.
- W1529881836 hasPublicationYear "2007" @default.
- W1529881836 type Work @default.
- W1529881836 sameAs 1529881836 @default.
- W1529881836 citedByCount "23" @default.
- W1529881836 countsByYear W15298818362012 @default.
- W1529881836 countsByYear W15298818362013 @default.
- W1529881836 countsByYear W15298818362014 @default.
- W1529881836 countsByYear W15298818362015 @default.
- W1529881836 countsByYear W15298818362016 @default.
- W1529881836 countsByYear W15298818362017 @default.
- W1529881836 countsByYear W15298818362021 @default.
- W1529881836 countsByYear W15298818362022 @default.
- W1529881836 crossrefType "journal-article" @default.
- W1529881836 hasAuthorship W1529881836A5036843120 @default.
- W1529881836 hasAuthorship W1529881836A5040504384 @default.
- W1529881836 hasAuthorship W1529881836A5045441660 @default.
- W1529881836 hasAuthorship W1529881836A5069458671 @default.
- W1529881836 hasBestOaLocation W15298818361 @default.
- W1529881836 hasConcept C104317684 @default.
- W1529881836 hasConcept C126322002 @default.
- W1529881836 hasConcept C135763542 @default.
- W1529881836 hasConcept C149737253 @default.
- W1529881836 hasConcept C180754005 @default.
- W1529881836 hasConcept C197754878 @default.
- W1529881836 hasConcept C2778163477 @default.
- W1529881836 hasConcept C2778270857 @default.
- W1529881836 hasConcept C2779134260 @default.
- W1529881836 hasConcept C2780745583 @default.
- W1529881836 hasConcept C54355233 @default.
- W1529881836 hasConcept C62746215 @default.
- W1529881836 hasConcept C71924100 @default.
- W1529881836 hasConcept C86803240 @default.
- W1529881836 hasConcept C90924648 @default.
- W1529881836 hasConceptScore W1529881836C104317684 @default.
- W1529881836 hasConceptScore W1529881836C126322002 @default.
- W1529881836 hasConceptScore W1529881836C135763542 @default.
- W1529881836 hasConceptScore W1529881836C149737253 @default.
- W1529881836 hasConceptScore W1529881836C180754005 @default.
- W1529881836 hasConceptScore W1529881836C197754878 @default.
- W1529881836 hasConceptScore W1529881836C2778163477 @default.
- W1529881836 hasConceptScore W1529881836C2778270857 @default.
- W1529881836 hasConceptScore W1529881836C2779134260 @default.
- W1529881836 hasConceptScore W1529881836C2780745583 @default.
- W1529881836 hasConceptScore W1529881836C54355233 @default.
- W1529881836 hasConceptScore W1529881836C62746215 @default.
- W1529881836 hasConceptScore W1529881836C71924100 @default.
- W1529881836 hasConceptScore W1529881836C86803240 @default.
- W1529881836 hasConceptScore W1529881836C90924648 @default.
- W1529881836 hasFunder F4320320720 @default.
- W1529881836 hasIssue "9" @default.