Impact of delayed effects on human old-age mortality

DOHaD delayed effects older age mortality patterns senescence

Journal

Demographic research
ISSN: 1435-9871
Titre abrégé: Demogr Res
Pays: Germany
ID NLM: 100964435

Informations de publication

Date de publication:
Historique:
entrez: 28 8 2019
pubmed: 28 8 2019
medline: 28 8 2019
Statut: ppublish

Résumé

There is growing empirical evidence supporting theories of developmental origins of health and disease (DOHaD). However, the implications of DOHaD conjectures for aggregate population patterns of human disease, disability, mortality and aging are poorly understood. We empirically test two predictions derived from a formal model of aggregate population-level impacts of DOHaD. This model predicts that populations potentially influenced by delayed effects should experience singularities in their adult mortality patterns that can be empirically detected from aggregate data. We test predictions using a large mortality database for populations in the Latin American and Caribbean region (LAC) spanning nearly one hundred years of mortality history. Results are consistent. within explicit bounds of uncertainty, with expected patterns. We find that younger cohorts in countries whose mortality decline starts more recently experience deceleration in survival gains at older ages, attenuation of the rate of aging at older ages and a decline in the association between early childhood and adult mortality. Results point to the importance of adverse early conditions for human longevity. Future research should shed light on the impact on morbidity, disability and healthy life expectancy. To our knowledge this is the first time that implications of DOHaD conjectures for populations' mortality patterns are formulated precisely and empirically tested with aggregate population data.

Sections du résumé

BACKGROUND BACKGROUND
There is growing empirical evidence supporting theories of developmental origins of health and disease (DOHaD). However, the implications of DOHaD conjectures for aggregate population patterns of human disease, disability, mortality and aging are poorly understood.
OBJECTIVE OBJECTIVE
We empirically test two predictions derived from a formal model of aggregate population-level impacts of DOHaD. This model predicts that populations potentially influenced by delayed effects should experience singularities in their adult mortality patterns that can be empirically detected from aggregate data.
METHODS METHODS
We test predictions using a large mortality database for populations in the Latin American and Caribbean region (LAC) spanning nearly one hundred years of mortality history.
RESULTS RESULTS
Results are consistent. within explicit bounds of uncertainty, with expected patterns. We find that younger cohorts in countries whose mortality decline starts more recently experience deceleration in survival gains at older ages, attenuation of the rate of aging at older ages and a decline in the association between early childhood and adult mortality.
CONCLUSIONS CONCLUSIONS
Results point to the importance of adverse early conditions for human longevity. Future research should shed light on the impact on morbidity, disability and healthy life expectancy.
CONTRIBUTION UNASSIGNED
To our knowledge this is the first time that implications of DOHaD conjectures for populations' mortality patterns are formulated precisely and empirically tested with aggregate population data.

Identifiants

pubmed: 31452626
doi: 10.4054/DemRes.2019.40.41
pmc: PMC6709713
mid: NIHMS1028562
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1167-1210

Subventions

Organisme : NICHD NIH HHS
ID : P2C HD041022
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG017266
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG052030
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG056608
Pays : United States

Références

Int J Epidemiol. 2012 Feb;41(1):219-23
pubmed: 22422456
Annu Rev Neurosci. 2001;24:1161-92
pubmed: 11520931
Br Med Bull. 2001;60:5-20
pubmed: 11809615
Pediatr Res. 2007 May;61(5 Pt 2):5R-10R
pubmed: 17413851
Science. 2004 Sep 17;305(5691):1736-9
pubmed: 15375259
CMAJ. 2000 Jul 11;163(1):49-56
pubmed: 10920732
Child Dev. 2010 Jan-Feb;81(1):41-79
pubmed: 20331654
J Epidemiol Community Health. 1978 Mar;32(1):34-7
pubmed: 262586
Soc Biol. 1981 Fall-Winter;28(3-4):187-216
pubmed: 7349697
Nature. 2004 Jul 22;430(6998):419-21
pubmed: 15269759
N Engl J Med. 1998 Jan 15;338(3):171-9
pubmed: 9428819
Popul Index. 1992 Summer;58(2):186-212
pubmed: 12285320
J Dev Orig Health Dis. 2012 Oct;3(5):380-6
pubmed: 23626899
Ann Nutr Metab. 2014;64 Suppl 1:8-17
pubmed: 25059801
Popul Stud (Camb). 1978 Jul;32(2):275-97
pubmed: 11630579
Demogr Res. 2013;29:543-578
pubmed: 25705120
Proc Natl Acad Sci U S A. 2006 Jan 10;103(2):498-503
pubmed: 16387863
Int J Epidemiol. 2012 Feb;41(1):116-23
pubmed: 22422450
Am J Clin Nutr. 1997 Aug;66(2):464S-477S
pubmed: 9250134
Public Health. 2012 Mar;126(3):185-189
pubmed: 22325676
J Hyg (Lond). 1934 Dec;34(4):433-57
pubmed: 20475246
PLoS One. 2014 Sep 19;9(9):e107653
pubmed: 25238154
Ann Nutr Metab. 2014;64 Suppl 1:26-34
pubmed: 25059803
Demography. 2000 Feb;37(1):53-72
pubmed: 10748989
Popul Stud (Camb). 2000 Nov;54(3):263-77
pubmed: 11640213

Auteurs

Andrea Verhulst (A)

Population Studies Center, University of Pennsylvania, Philadelphia, USA.

Hiram Beltran-Sanchez (H)

Department of Community Health Sciences, Fielding School of Public Health and California Center for Population Research, UCLA, Los Angeles, USA.

Alberto Palloni (A)

Labor and Population Unit, RAND Corporation and Center for Demography and Health of Aging, University of Wisconsin-Madison, USA.

Classifications MeSH