M. Pepin et al., STRATEGIES AND OUTCOMES OF PRENATAL-DIAGNOSIS FOR OSTEOGENESIS-IMPERFECTA - A REVIEW OF BIOCHEMICAL AND MOLECULAR STUDIES COMPLETED IN 129 PREGNANCIES, Prenatal diagnosis, 17(6), 1997, pp. 559-570
We completed prenatal diagnostic studies from 129 pregnancies at risk
for osteogenesis imperfecta (OI). Studies in 107 pregnancies were comp
leted by analysis of collagen synthesized by cells cultured from chori
onic villus biopsies and the remaining 22 used direct mutation identif
ication or analysis of polymorphic restriction sites in the COL1A1 gen
e of type I collagen. The vast majority of studies (n=113) were obtain
ed to identify fetuses with OI type II (the perinatal lethal form) and
some fetuses affected with OI type III or IV (the deforming varieties
). Of the 50 couples who had had one previous affected pregnancy with
the lethal form of OI, one had a second affected pregnancy, a rate of
2 per cent. Two of the seven unaffected couples (28 per cent) who had
had two previous affected pregnancies with OI type II had a third affe
cted pregnancy; none of the three with two previous pregnancies with O
I type III had a third. Pregnancies at risk for OI type I could not be
ascertained reliably by biochemical analysis of cultured CVS cells bu
t were identified by direct analysis of the causative mutation or the
use of linked markers in families. All prenatal diagnostic studies wer
e undertaken only after earlier diagnostic studies (biochemical or mol
ecular) had been completed on the proband, a necessary strategy for ac
curate results. In all pregnancies at risk for OI type II, OI type III
, and OI type IV studied with biochemical strategies and in pregnancie
s at risk for OI type I studied with molecular techniques, there were
neither false-negative nor false-positive results. Diagnostic informat
ion can be obtained within 20-30 days of biopsy using biochemical tech
niques and within 10-14 days when molecular strategies are used. (C) 1
997 by John Wiley & Sons, Ltd.