Bromocriptine Improves Central Aortic Stiffness in Adolescents With Type 1 Diabetes: Arterial Health Results From the BCQR-T1D Study.


Journal

Hypertension (Dallas, Tex. : 1979)
ISSN: 1524-4563
Titre abrégé: Hypertension
Pays: United States
ID NLM: 7906255

Informations de publication

Date de publication:
02 2023
Historique:
pmc-release: 01 02 2024
pubmed: 7 12 2022
medline: 21 1 2023
entrez: 6 12 2022
Statut: ppublish

Résumé

The presence of vascular dysfunction is a well-recognized feature in youth with type 1 diabetes (T1D), accentuating their lifetime risk of cardiovascular events. Therapeutic strategies to mitigate vascular dysfunction are a high clinical priority. In the bromocriptine quick release T1D study (BCQR-T1D), we tested the hypothesis that BCQR would improve vascular health in youth with T1D. BCQR-T1D was a placebo-controlled, random-order, double-blinded, cross-over study investigating the cardiovascular and metabolic impact of BCQR in T1D. Adolescents in the BCQR-T1D study were randomized 1:1 to phase-1: 4 weeks of BCQR or placebo after which blood pressure and central aortic stiffness measurements by pulse wave velocity, relative area change, and distensibility from phase-contrast magnetic resonance imaging were performed. Following a 4-week washout period, phase 2 was performed in identical fashion with the alternate treatment. Thirty-four adolescents (mean age 15.9±2.6 years, hemoglobin A1c 8.6±1.1%, body mass index percentile 71.4±26.1, median T1D duration 5.8 years) with T1D were enrolled and had magnetic resonance imaging data available. Compared with placebo, BCQR therapy decreased systolic (∆=-5 mmHg [95% CI, -3 to -7]; BCQR improved blood pressure and central and peripheral aortic stiffness and pressure hemodynamics in adolescents with T1D over 4 weeks versus placebo. BCQR may improve aortic stiffness in youth with T1D, supporting future longer-term studies.

Sections du résumé

BACKGROUND
The presence of vascular dysfunction is a well-recognized feature in youth with type 1 diabetes (T1D), accentuating their lifetime risk of cardiovascular events. Therapeutic strategies to mitigate vascular dysfunction are a high clinical priority. In the bromocriptine quick release T1D study (BCQR-T1D), we tested the hypothesis that BCQR would improve vascular health in youth with T1D.
METHODS
BCQR-T1D was a placebo-controlled, random-order, double-blinded, cross-over study investigating the cardiovascular and metabolic impact of BCQR in T1D. Adolescents in the BCQR-T1D study were randomized 1:1 to phase-1: 4 weeks of BCQR or placebo after which blood pressure and central aortic stiffness measurements by pulse wave velocity, relative area change, and distensibility from phase-contrast magnetic resonance imaging were performed. Following a 4-week washout period, phase 2 was performed in identical fashion with the alternate treatment.
RESULTS
Thirty-four adolescents (mean age 15.9±2.6 years, hemoglobin A1c 8.6±1.1%, body mass index percentile 71.4±26.1, median T1D duration 5.8 years) with T1D were enrolled and had magnetic resonance imaging data available. Compared with placebo, BCQR therapy decreased systolic (∆=-5 mmHg [95% CI, -3 to -7];
CONCLUSIONS
BCQR improved blood pressure and central and peripheral aortic stiffness and pressure hemodynamics in adolescents with T1D over 4 weeks versus placebo. BCQR may improve aortic stiffness in youth with T1D, supporting future longer-term studies.

Identifiants

pubmed: 36472197
doi: 10.1161/HYPERTENSIONAHA.122.19547
pmc: PMC9852005
mid: NIHMS1844066
doi:

Substances chimiques

Bromocriptine 3A64E3G5ZO

Types de publication

Randomized Controlled Trial Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

482-491

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK048520
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK091553
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK116073
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK116720
Pays : United States
Organisme : NIDDK NIH HHS
ID : R21 DK129720
Pays : United States
Organisme : NHLBI NIH HHS
ID : K24 HL145076
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK129211
Pays : United States

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Auteurs

Michal Schäfer (M)

Division of Pediatric Cardiology, Department of Pediatrics (M.S.), University of Colorado - School of Medicine, Aurora.

Lorna P Browne (LP)

Department of Radiology (L.P.B., A.J.B.), University of Colorado - School of Medicine, Aurora.

Uyen Truong (U)

Department of Cardiology, Children's Hospital of Richmond at Virginia Commonwealth University (U.T.).

Petter Bjornstad (P)

Section of Pediatric Endocrinology, Department of Pediatrics (P.B., S.T., A.B., K.J.N.), University of Colorado - School of Medicine, Aurora.

Shoshana Tell (S)

Section of Pediatric Endocrinology, Department of Pediatrics (P.B., S.T., A.B., K.J.N.), University of Colorado - School of Medicine, Aurora.

Janet Snell-Bergeon (J)

Barbara Davis Center, Department of Medicine (J.S.-B.), University of Colorado - School of Medicine, Aurora.

Amy Baumgartner (A)

Section of Pediatric Endocrinology, Department of Pediatrics (P.B., S.T., A.B., K.J.N.), University of Colorado - School of Medicine, Aurora.

Kendall S Hunter (KS)

Department of Bioengineering, University of Colorado Denver (K.S.H., A.J.B.).

Jane E B Reusch (JEB)

Division of Endocrinology, Department of Medicine (J.E.B.R., I.E.S.), University of Colorado - School of Medicine, Aurora.
Center for Women's Health Research (J.E.B.R., I.E.S.), University of Colorado - School of Medicine, Aurora.
Section of Endocrinology, Rocky Mountain Regional VAMC, Aurora, CO (J.E.B.R., I.E.S.).

Alex J Barker (AJ)

Department of Radiology (L.P.B., A.J.B.), University of Colorado - School of Medicine, Aurora.
Department of Bioengineering, University of Colorado Denver (K.S.H., A.J.B.).

Kristen J Nadeau (KJ)

Section of Pediatric Endocrinology, Department of Pediatrics (P.B., S.T., A.B., K.J.N.), University of Colorado - School of Medicine, Aurora.

Irene E Schauer (IE)

Division of Endocrinology, Department of Medicine (J.E.B.R., I.E.S.), University of Colorado - School of Medicine, Aurora.
Center for Women's Health Research (J.E.B.R., I.E.S.), University of Colorado - School of Medicine, Aurora.
Section of Endocrinology, Rocky Mountain Regional VAMC, Aurora, CO (J.E.B.R., I.E.S.).

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