A discussion of statistical methods to characterise early growth and its impact on bone mineral content later in childhood.


Journal

Annals of human biology
ISSN: 1464-5033
Titre abrégé: Ann Hum Biol
Pays: England
ID NLM: 0404024

Informations de publication

Date de publication:
Feb 2019
Historique:
pubmed: 6 2 2019
medline: 13 7 2019
entrez: 6 2 2019
Statut: ppublish

Résumé

Many statistical methods are available to model longitudinal growth data and relate derived summary measures to later outcomes. To apply and compare commonly used methods to a realistic scenario including pre- and postnatal data, missing data, and confounders. Data were collected from 753 offspring in the Southampton Women's Survey with measurements of bone mineral content (BMC) at age 6 years. Ultrasound measures included crown-rump length (11 weeks' gestation) and femur length (19 and 34 weeks' gestation); postnatally, infant length (birth, 6 and 12 months) and height (2 and 3 years) were measured. A residual growth model, two-stage multilevel linear spline model, joint multilevel linear spline model, SITAR and a growth mixture model were used to relate growth to 6-year BMC. Results from the residual growth, two-stage and joint multilevel linear spline models were most comparable: an increase in length at all ages was positively associated with BMC, the strongest association being with later growth. Both SITAR and the growth mixture model demonstrated that length was positively associated with BMC. Similarities and differences in results from a variety of analytic strategies need to be understood in the context of each statistical methodology.

Sections du résumé

BACKGROUND BACKGROUND
Many statistical methods are available to model longitudinal growth data and relate derived summary measures to later outcomes.
AIM OBJECTIVE
To apply and compare commonly used methods to a realistic scenario including pre- and postnatal data, missing data, and confounders.
SUBJECTS AND METHODS METHODS
Data were collected from 753 offspring in the Southampton Women's Survey with measurements of bone mineral content (BMC) at age 6 years. Ultrasound measures included crown-rump length (11 weeks' gestation) and femur length (19 and 34 weeks' gestation); postnatally, infant length (birth, 6 and 12 months) and height (2 and 3 years) were measured. A residual growth model, two-stage multilevel linear spline model, joint multilevel linear spline model, SITAR and a growth mixture model were used to relate growth to 6-year BMC.
RESULTS RESULTS
Results from the residual growth, two-stage and joint multilevel linear spline models were most comparable: an increase in length at all ages was positively associated with BMC, the strongest association being with later growth. Both SITAR and the growth mixture model demonstrated that length was positively associated with BMC.
CONCLUSIONS CONCLUSIONS
Similarities and differences in results from a variety of analytic strategies need to be understood in the context of each statistical methodology.

Identifiants

pubmed: 30719940
doi: 10.1080/03014460.2019.1574896
pmc: PMC6518455
mid: EMS82397
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

17-26

Subventions

Organisme : Medical Research Council
ID : MR/R010692/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : G1000726
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P023347/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UP_1005/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12013/9
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UP_A620_1017
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12011/4
Pays : United Kingdom
Organisme : NIA NIH HHS
ID : P01 AG043362
Pays : United States
Organisme : Medical Research Council
ID : MR/M012069/1
Pays : United Kingdom

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Auteurs

Sarah R Crozier (SR)

a MRC Lifecourse Epidemiology Unit, Southampton General Hospital , University of Southampton , Southampton , UK.

William Johnson (W)

b School of Sport, Exercise and Health Sciences , Loughborough University , Loughborough, Leicestershire , UK.

Tim J Cole (TJ)

c Population, Policy and Practice Programme , UCL Great Ormond Street Institute of Child Health , London , UK.

Corrie Macdonald-Wallis (C)

d MRC Integrative Epidemiology Unit, Oakfield House , University of Bristol , Bristol , UK.
e Department of Population Health Sciences , Oakfield House , Bristol , UK.

Graciela Muniz-Terrera (G)

f Centre for Clinical Brain Sciences , University of Edinburgh , Edinburgh , UK.

Hazel M Inskip (HM)

a MRC Lifecourse Epidemiology Unit, Southampton General Hospital , University of Southampton , Southampton , UK.

Kate Tilling (K)

d MRC Integrative Epidemiology Unit, Oakfield House , University of Bristol , Bristol , UK.
e Department of Population Health Sciences , Oakfield House , Bristol , UK.

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Classifications MeSH