Your browser doesn't support javascript.
loading
Influence of chronotype on pain incidence during early adolescence.
Li, Rui; Groenewald, Cornelius; Tham, See Wan; Rabbitts, Jennifer A; Ward, Teresa M; Palermo, Tonya M.
Afiliação
  • Li R; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, WA, United States.
  • Groenewald C; Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, United States.
  • Tham SW; Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, United States.
  • Rabbitts JA; Center for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, WA, United States.
  • Ward TM; Department of Anesthesiology and Pain Medicine, University of Washington School of Medicine, Seattle, WA, United States.
  • Palermo TM; Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Pain ; 2024 May 28.
Article em En | MEDLINE | ID: mdl-38809249
ABSTRACT
ABSTRACT During adolescence major shifts in sleep and circadian systems occur with a notable circadian phase delay. Yet, the circadian influence on pain during early adolescence is largely unknown. Using 2 years of data from the Adolescent Brain Cognitive Development study, we investigated the impact of chronotype on pain incidence, moderate-to-severe pain, and multiregion pain 1 year later in U.S. adolescents. Based on the Munich ChronoType Questionnaire, chronotype was calculated as the midpoint between sleep onset and offset on free days, corrected for sleep debt over the week. Adolescents reported pain presence over the past month, and if present, rated pain intensity (0-10 numerical rating scale; ≥ 4 defined as moderate-to-severe pain) and body site locations (Collaborative Health Outcomes Information Registry Body Map; ≥2 regions defined as multiregion pain). Three-level random intercept logistic regression models were specified for each pain outcome, adjusting for baseline sociodemographic and developmental characteristics. Among 5991 initially pain-free adolescents (mean age 12.0 years, SD 0.7), the mean chronotype was 359 am (SD 97 minutes), and the 1-year incidence of pain, moderate-to-severe pain, and multiregion pain was 24.4%, 15.2%, and 13.5%, respectively. Each hour later chronotype at baseline was associated with higher odds of developing any pain (odds ratio [OR] = 1.06, 95% confidence interval [CI] = 1.01, 1.11), moderate-to-severe pain (OR = 1.10, 95% CI = 1.05-1.17), and multiregion pain (OR = 1.08, 95% CI = 1.02-1.14) during 1-year follow-up. In this diverse U.S. adolescent sample, later chronotype predicted higher incidence of new-onset pain.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article