Mortality from congenital anomalies

Authors
Citation
J. Dolejs, Mortality from congenital anomalies, MECH AGE D, 105(3), 1998, pp. 319-332
Citations number
9
Categorie Soggetti
Cell & Developmental Biology
Journal title
MECHANISMS OF AGEING AND DEVELOPMENT
ISSN journal
00476374 → ACNP
Volume
105
Issue
3
Year of publication
1998
Pages
319 - 332
Database
ISI
SICI code
0047-6374(19981116)105:3<319:MFCA>2.0.ZU;2-6
Abstract
Research has been conducted on the relationship between postnatal mortality from dominant causes and age, using data from the US, Japan and former Cze choslovakia, during the period 1979-1991. The logarithm of a total mortalit y, total mortality excluding deaths caused by accidents, logarithm of morta lity caused by congenital anomalies, logarithm of mortality caused by other respiratory diseases and logarithm of mortality caused by diseases of the nervous system fell linearly with the logarithm of age, during the interval of 0-10 years. Congenital anomalies showed a log-log mortality experience that was linear until the age of 45, in some populations. This linear log-l og dependence corresponds to the two-parametrical Weibull distribution, if the slope is greater than -1. However, the logarithm of mortality from cong enital anomalies declined with the slope equal to -1. In those congenital a nomalies with the slope equal to -1, the logarithm of number of deaths in 1 year declined with the logarithm of age (that quantity corresponds to the density of defects in the theory of reliability). Consequently, there was a pplied another distribution function described in this paper. The number of deaths due to congenital anomalies over the period of 1 year was inversely proportional to the age at death. A hypothesis that the individual has his /her span of life strictly determined by the level of malformation at the m oment of birth might explain the fact. A natural consequence of this hypoth esis together with the facts mentioned above is as follows: the more seriou s the defect was, the more frequent this defect was. (C) 1998 Elsevier Scie nce Ireland Ltd. All rights reserved.