Evaluation of the longitudinal change in health behavior profiles across treatment groups in the TODAY clinical trial.


Journal

Pediatric diabetes
ISSN: 1399-5448
Titre abrégé: Pediatr Diabetes
Pays: Denmark
ID NLM: 100939345

Informations de publication

Date de publication:
03 2020
Historique:
received: 10 04 2019
revised: 28 08 2019
accepted: 18 09 2019
pubmed: 31 12 2019
medline: 17 2 2021
entrez: 31 12 2019
Statut: ppublish

Résumé

Individual health behaviors (ie, eating habits and sedentary lifestyle) are associated with type 2 diabetes (T2D). Health behavior profiles specific to adolescents with T2D have not been described. To identify health behavior profiles in adolescents with T2D and examine how these profiles change over time. Diet (via food frequency questionnaire) and activity behaviors (via 3-day physical activity recall) examined at baseline, 6 months, and 24 months from participants in the the Treatment Options for T2D in Adolescents and Youth (TODAY) study were used for this analysis. Latent profile analysis identified profiles of health behaviors within three time points, and latent transition probabilities were estimated to examine the change from baseline to 6 months (n = 450) and baseline to 24 months (n = 415). Multinomial logistic regressions were used to examine if the assigned TODAY treatment group (Metformin [Met], Met + Rosiglitazone [Rosi], or Met + Lifestyle) predicted change in health behavior profiles. Three profiles emerged: "most sedentary," "healthy eaters," and "active and eat most." At 6 months, 50% of males and 29% of females in the Met + Lifestyle treatment group improved in their health behavior profile. Among males only, the Met + Lifestyle treatment group were more likely to improve their profiles from baseline to 6 months (P = .01). Three health behavior profiles emerged and shifted over time. A high quality, lifestyle intervention had little effect on improving health behavior profiles. Optimizing outcomes in youth with T2D might require more robust and multifaceted interventions beyond family-level lifestyle, including more extensive psychosocial intervention, novel medication regimen, or bariatric surgery.

Sections du résumé

BACKGROUND
Individual health behaviors (ie, eating habits and sedentary lifestyle) are associated with type 2 diabetes (T2D). Health behavior profiles specific to adolescents with T2D have not been described.
OBJECTIVE
To identify health behavior profiles in adolescents with T2D and examine how these profiles change over time.
METHODS
Diet (via food frequency questionnaire) and activity behaviors (via 3-day physical activity recall) examined at baseline, 6 months, and 24 months from participants in the the Treatment Options for T2D in Adolescents and Youth (TODAY) study were used for this analysis. Latent profile analysis identified profiles of health behaviors within three time points, and latent transition probabilities were estimated to examine the change from baseline to 6 months (n = 450) and baseline to 24 months (n = 415). Multinomial logistic regressions were used to examine if the assigned TODAY treatment group (Metformin [Met], Met + Rosiglitazone [Rosi], or Met + Lifestyle) predicted change in health behavior profiles.
RESULTS
Three profiles emerged: "most sedentary," "healthy eaters," and "active and eat most." At 6 months, 50% of males and 29% of females in the Met + Lifestyle treatment group improved in their health behavior profile. Among males only, the Met + Lifestyle treatment group were more likely to improve their profiles from baseline to 6 months (P = .01).
CONCLUSIONS
Three health behavior profiles emerged and shifted over time. A high quality, lifestyle intervention had little effect on improving health behavior profiles. Optimizing outcomes in youth with T2D might require more robust and multifaceted interventions beyond family-level lifestyle, including more extensive psychosocial intervention, novel medication regimen, or bariatric surgery.

Identifiants

pubmed: 31886931
doi: 10.1111/pedi.12976
pmc: PMC7597379
mid: NIHMS1637321
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

224-232

Subventions

Organisme : NCRR NIH HHS
ID : UL1 RR024153
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061239
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR025758
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061254
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024134
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061212
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061242
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR001066
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR000125
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024989
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR014467
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK048520
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002548
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR025780
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024992
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK036836
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024139
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR000036
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK061230
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR000069
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR000043
Pays : United States

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Jill L Kaar (JL)

Department of Pediatrics, Division of Endocrinology, University of Colorado School of Medicine, Aurora, Colorado.

Sarah J Schmiege (SJ)

Department of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado.

Kimberly Drews (K)

The Biostatistics Center, George Washington University, Washington DC.

Janine Higgins (J)

Department of Pediatrics, Division of Endocrinology, University of Colorado School of Medicine, Aurora, Colorado.

Natalie Walders-Abramson (N)

Department of Pediatrics, Division of Endocrinology, University of Colorado School of Medicine, Aurora, Colorado.

Elvira Isganaitis (E)

Harvard Medical School, Boston, Massachusetts.
Joslin Diabetes Center, Boston, Massachusetts.

Steven M Willi (SM)

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Marsha D Marcus (MD)

Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

Philip S Zeitler (PS)

Department of Pediatrics, Division of Endocrinology, University of Colorado School of Medicine, Aurora, Colorado.

Megan M Kelsey (MM)

Department of Pediatrics, Division of Endocrinology, University of Colorado School of Medicine, Aurora, Colorado.

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