Elevated maternal age-specific rates of down syndrome liveborn offspring of women of Mexican and Central American origin in California

Citation
Eb. Hook et al., Elevated maternal age-specific rates of down syndrome liveborn offspring of women of Mexican and Central American origin in California, PRENAT DIAG, 19(3), 1999, pp. 245-251
Citations number
18
Categorie Soggetti
Reproductive Medicine","Medical Research Diagnosis & Treatment
Journal title
PRENATAL DIAGNOSIS
ISSN journal
01973851 → ACNP
Volume
19
Issue
3
Year of publication
1999
Pages
245 - 251
Database
ISI
SICI code
0197-3851(199903)19:3<245:EMAROD>2.0.ZU;2-S
Abstract
Background: maternal age-specific rates of Down syndrome livebirths are wid ely utilized in personal and policy decisions concerning provision of and e lection of prenatal cytogenetic diagnostic services. The only extensive ref erence data available are on those of primarily European ancestral origin. In the absence of definitive evidence of any ethnic, racial or environmenta l influence upon rates (other than those associated with age) these rate sc hedules have been widely applied to those of all national origins. Methods: available materal age-specific data on livebirths from intensive s tudies on those of Hispanic (primarily of Mexican and Central American back ground) and of other origin in populations in the U.S.A. with likely comple te ascertainment were analysed. The numbers observed were compared with (i) those predicted from established published rate schedules in those of prim arily European origin, and (ii) with the observations on livebirths of non- Hispanic European origin in the same population as the Hispanic live births . Results: in comparisons with the numbers predicted from published rates, ob served numbers of case among Hispanic live births were increased by 19 per cent (SE 0.06) in younger mothers, 23 per cent in older mothers (SE 0.07) a nd 20 per cent (SE 0.04) in those of all ages. Comparisons with observed ra tes in those of Hispanic origin with those observed in non-Hispanic births in the same time intervals and populations indicated that the excess rates in Hispanics were not attributable to some local factor increasing rates in all ethnic groups at least among those under 35. Conclusions: data on mothers of Mexican and Central American origin residin g in the U.S.A. indicate maternal age-specific rates of Down syndrome in li ve births about 20 per cent greater than those in published rate schedules on Down syndrome, widely used in decisions concerning election or provison of prenatal diagnostic services. The reason for this difference remains unk nown. Copyright (C) 1999 John Wiley & Sons, Ltd.