Prediction of large-for-gestational age infants in relation to hyperglycemia in pregnancy - A comparison of statistical models.


Journal

Diabetes research and clinical practice
ISSN: 1872-8227
Titre abrégé: Diabetes Res Clin Pract
Pays: Ireland
ID NLM: 8508335

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 11 10 2020
accepted: 19 07 2021
pubmed: 25 7 2021
medline: 25 11 2021
entrez: 24 7 2021
Statut: ppublish

Résumé

Using data from a large multi-centre cohort, we aimed to create a risk prediction model for large-for-gestational age (LGA) infants, using both logistic regression and naïve Bayes approaches, and compare the utility of these two approaches. We have compared the two techniques underpinning machine learning: logistic regression (LR) and naïve Bayes (NB) in terms of their ability to predict large-for-gestational age (LGA) infants. Using data from five centres involved in the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study, we developed LR and NB models and compared the predictive ability and stability between the models. Models were developed combining the risks of hyperglycaemia (assessed in three forms: IADPSG GDM yes/no, GDM subtype, OGTT z-score quintiles), demographic and clinical variables as potential predictors. The two approaches resulted in similar estimates of LGA risk (intraclass correlation coefficient 0.955, 95% CI 0.952, 0.958) however the AUROC for the LR model was significantly higher (0.698 vs 0.682; p < 0.001). When comparing the three LR models, use of individual OGTT z-score quintiles resulted in statistically higher AUROCs than the other two models. Logistic regression can be used with confidence to assess the relationship between clinical and biochemical variables and outcome.

Identifiants

pubmed: 34302910
pii: S0168-8227(21)00334-X
doi: 10.1016/j.diabres.2021.108975
pii:
doi:

Substances chimiques

Blood Glucose 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108975

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kristen S Gibbons (KS)

Faculty of Medicine, The University of Queensland, South Brisbane, Q 4051, Australia. Electronic address: k.gibbons@uq.edu.au.

Allan M Z Chang (AMZ)

Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong Special Administrative Region.

Ronald C W Ma (RCW)

Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong Special Administrative Region; Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong Special Administrative Region; Chinese University of Hong Kong-Shanghai Jiao Tong University Joint Research Centre in Diabetes Genomics and Precision Medicine, Hong Kong Institute of Diabetes and Obesity, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong Special Administrative Region.

Wing Hung Tam (WH)

Department of Obstetrics and Gynecology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong Special Administrative Region.

Patrick M Catalano (PM)

Department of Obstetrics and Gynecology, Mother Infant Research Institute, Tufts Medical Center, Boston, MA, USA.

David A Sacks (DA)

Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.

Julia Lowe (J)

Faculty of Health and Medicine, University of Newcastle, Newcastle, Australia.

H David McIntyre (H)

Faculty of Medicine, The University of Queensland, South Brisbane, Q 4051, Australia.

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