TY - JOUR
T1 - Major gene segregation of actinic prurigo among north American Indians in Saskatchewan
AU - Schnell, Audrey H.
AU - Elston, Robert C.
AU - Hull, Peter R.
AU - Lane, Peter R.
PY - 2000/5/29
Y1 - 2000/5/29
N2 - Actinic prurigo is an idiopathic, familial photodermatosis seen especially in American Indians. Segregation analysis was performed on 12 Saskatchewan pedigrees with American Indian ancestry, comprising a total of 1,148 individuals, ascertained via probands diagnosed with actinic prurigo. Although a high degree of familial aggregation has been noted in the past and dominant inheritance has been suggested, no formal segregation analysis has been attempted. Actinic prurigo has a variable age of onset and, therefore, age at the time of censoring must be taken into account in the analysis. However, as these ages of 57% of the unaffected individuals were missing, an algorithm was devised to impute the missing ages from known birth years in the family based on the age differences among relatives and spouses. Using these imputed ages, simple dominant inheritance with incomplete penetrance and a single age of onset distribution was found. The method for imputing the ages at examination was evaluated, as was the correction for ascertainment, by using alternative methods and comparing the results. Regardless of the method used, a dominant mode of inheritance without any multifactoral component remained the best hypothesis. (C) 2000 Wiley-Liss, Inc.
AB - Actinic prurigo is an idiopathic, familial photodermatosis seen especially in American Indians. Segregation analysis was performed on 12 Saskatchewan pedigrees with American Indian ancestry, comprising a total of 1,148 individuals, ascertained via probands diagnosed with actinic prurigo. Although a high degree of familial aggregation has been noted in the past and dominant inheritance has been suggested, no formal segregation analysis has been attempted. Actinic prurigo has a variable age of onset and, therefore, age at the time of censoring must be taken into account in the analysis. However, as these ages of 57% of the unaffected individuals were missing, an algorithm was devised to impute the missing ages from known birth years in the family based on the age differences among relatives and spouses. Using these imputed ages, simple dominant inheritance with incomplete penetrance and a single age of onset distribution was found. The method for imputing the ages at examination was evaluated, as was the correction for ascertainment, by using alternative methods and comparing the results. Regardless of the method used, a dominant mode of inheritance without any multifactoral component remained the best hypothesis. (C) 2000 Wiley-Liss, Inc.
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U2 - 10.1002/(SICI)1096-8628(20000529)92:3<212::AID-AJMG10>3.0.CO;2-W
DO - 10.1002/(SICI)1096-8628(20000529)92:3<212::AID-AJMG10>3.0.CO;2-W
M3 - Article
C2 - 10817657
AN - SCOPUS:0034729392
SN - 0148-7299
VL - 92
SP - 212
EP - 219
JO - American Journal of Medical Genetics
JF - American Journal of Medical Genetics
IS - 3
ER -