Asamoah A, Wyatt R J, Julian B A, Quiggins P A, Wilson A F, Elston R C
Department of Biometry and Genetics, Louisiana State University Medical Center, New Orleans 70112.
Am J Med Genet. 1987 Aug;27(4):857-66. doi: 10.1002/ajmg.1320270413.
Plasma IgA concentration was determined on 94 individuals of an eastern Kentucky family (IGANI) with some members having clinical and biopsy-proven IgA nephropathy, and on 197 individuals of a large Louisiana family (HGAR29) with no clinical history of IgA nephropathy but on whom 30 polymorphic markers had previously been typed. Pedigree segregation analysis was used to fit a major gene model, and a moderately large lod score for linkage to the ABO locus (1.50 at 0% recombination) suggested the existence of a recessive allele for high plasma IgA concentration. This allele is only slightly more prevalent in pedigree IGANI than in pedigree HGAR29, indicating that it is a minor, rather than a major, etiologic factor in IgA nephropathy.
对肯塔基州东部一个家族(IGANI)的94名成员测定了血浆IgA浓度,该家族部分成员患有经临床和活检证实的IgA肾病;还对路易斯安那州一个大家族(HGAR29)的197名成员进行了测定,该家族无IgA肾病临床病史,但之前已对其30个多态性标记进行了分型。采用系谱分离分析来拟合一个主基因模型,与ABO位点连锁的适度高的lod分数(重组率为0%时为1.50)表明存在一个导致血浆IgA浓度升高的隐性等位基因。该等位基因在IGANI家族中的流行程度仅略高于HGAR29家族,这表明它是IgA肾病的一个次要而非主要病因。