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Is genetic susceptibility to pre‐eclampsia conferred by homozygosity for the same single recessive gene in mother and fetus?
Author(s) -
LISTON WILLIAM A.,
KILPATRICK DAVID C.
Publication year - 1991
Publication title -
bjog: an international journal of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.157
H-Index - 164
eISSN - 1471-0528
pISSN - 1470-0328
DOI - 10.1111/j.1471-0528.1991.tb15358.x
Subject(s) - mendelian inheritance , eclampsia , genetics , inheritance (genetic algorithm) , genetic model , biology , fetus , incidence (geometry) , disease , genetic predisposition , gene , multifactorial inheritance , allele , pregnancy , genotype , medicine , single nucleotide polymorphism , mathematics , geometry
Abstract Objective— To determine whether any simple, purely genetic mechanism can account for susceptibility to pre‐eclampsia. Design— Six simple Mendelian models of inheritance were considered, and pre‐dictions concerning the incidence of pre‐eclampsia in various family members of index cases were calculated for each genetic model. Data were then extracted from published family studies in which a suitable disease definition had been used, and compared to our theoretical expectations. Results— Only one of the genetic models considered, in which both mother and fetus must express the same recessive gene to confer susceptibility, was consistent with the observed incidence values for relatives of index cases. This model was also consistent with the putative association with HLA‐DR4, but could not account for the comparative rarity of pre‐eclampsia in parous women. Conclusion— Homozygosity for a single recessive gene shared by mother and fetus, unlike five other genetic mechanisms tested, is consistent with published family studies in pre‐eclampsia, and should be considered the best working hypothesis at present.