Core Concepts
Changes in growth hormone mediators impact glycemic control in youth-onset T2D.
Abstract
TOPLINE:
Plasma growth hormone mediators like GHR and IGFBP-1 linked to glycemic failure in youth-onset T2D.
METHODOLOGY:
Youth T2D often post-puberty, suggesting hormonal influence.
Study on 398 youths (10-17 years) with T2D <2 years.
Followed for 3.9 years, assessing various factors.
Primary outcomes: glycemic failure, metabolic decompensation.
TAKEAWAY:
46% experienced glycemic failure, 54% retained control.
Those with failure had lower IGF-1, higher GHR, and IGFBP-1 levels.
Higher IGF-1 linked to lower odds of failure.
Increased GHR and IGFBP-1 levels linked to higher odds of failure.
IN PRACTICE:
GHR level identified as a novel glycemic control biomarker in youth T2D.
Future research needed on growth hormone mediators in diabetes complications.
SOURCE:
Study led by Chang Lu, MD, Boston Children's Hospital.
LIMITATIONS:
No control group, mainly late puberty youth.
Only circulating mediators measured, limiting hormone source identification.
DISCLOSURES:
Authors received grants from NIH and NIDDK during the study.
Stats
Changes in plasma growth hormone mediators linked to glycemic failure in youth-onset T2D.
46% of participants experienced glycemic failure.
Increased IGF-1 levels associated with lower odds of glycemic failure.
Higher GHR and IGFBP-1 levels linked to higher odds of glycemic failure.
Quotes
"Our study has identified GHR level as a novel biomarker of decrease in glycemic control in youths with T2D." - Study authors