Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency

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Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency. / Jørgensen, Nanna Thurmann; Boesen, Victor Brun; Borresen, Stina Willemoes; Christoffersen, Thea; Jørgensen, Niklas Rye; Plomgaard, Peter; Christoffersen, Christina; Watt, Torquil; Feldt-Rasmussen, Ulla; Klose, Marianne.

In: Endocrine, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jørgensen, NT, Boesen, VB, Borresen, SW, Christoffersen, T, Jørgensen, NR, Plomgaard, P, Christoffersen, C, Watt, T, Feldt-Rasmussen, U & Klose, M 2024, 'Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency', Endocrine. https://doi.org/10.1007/s12020-024-03711-9

APA

Jørgensen, N. T., Boesen, V. B., Borresen, S. W., Christoffersen, T., Jørgensen, N. R., Plomgaard, P., Christoffersen, C., Watt, T., Feldt-Rasmussen, U., & Klose, M. (Accepted/In press). Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency. Endocrine. https://doi.org/10.1007/s12020-024-03711-9

Vancouver

Jørgensen NT, Boesen VB, Borresen SW, Christoffersen T, Jørgensen NR, Plomgaard P et al. Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency. Endocrine. 2024. https://doi.org/10.1007/s12020-024-03711-9

Author

Jørgensen, Nanna Thurmann ; Boesen, Victor Brun ; Borresen, Stina Willemoes ; Christoffersen, Thea ; Jørgensen, Niklas Rye ; Plomgaard, Peter ; Christoffersen, Christina ; Watt, Torquil ; Feldt-Rasmussen, Ulla ; Klose, Marianne. / Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency. In: Endocrine. 2024.

Bibtex

@article{6f18c9f6db254b79a46471b38ac50baf,
title = "Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency",
abstract = "Purpose: Studies have suggested improved metabolic profiles in patients with adrenal insufficiency treated with dual-release hydrocortisone (DR-HC) compared with conventional hydrocortisone (C-HC). This study investigates the effect of DR-HC compared with C-HC treatment on five health variables: diurnal salivary cortisol/cortisone, body composition, bone health, glucose metabolism, lipids, and blood pressure. Methods: Prospective study of 27 participants (24 men) with secondary adrenal insufficiency with measurements during stable C-HC and 16 weeks after treatment switch to DR-HC. Outcomes: Diurnal salivary-cortisol/cortisone, body composition assessed by Dual-Energy X-ray absorptiometry scan, bone status indices (serum type I N-terminal procollagen [PINP], collagen type I cross-linked C-telopeptide [CTX], osteocalcin, receptor activator kappa-B [RANK] ligand, osteoprotegerin, and sclerostin), lipids, haemoglobin A1c (HbA1c), and 24-hour blood pressure. Results: After the switch to DR-HC, the diurnal salivary-cortisol area under the curve (AUC) decreased non-significantly (mean difference: −55.9 nmol/L/day, P = 0.06). The salivary-cortisone-AUC was unchanged. Late-evening salivary-cortisol and cortisone were lower (−1.6 and −1.7 nmol/L, P = 0.002 and 0.004). Total and abdominal fat mass (−1.5 and −0.5 kg, P = 0.003 and 0.02), HbA1c (−1.2 mmol/mol, P = 0.02), and osteocalcin decreased (−7.0 µg/L, P = 0.03) whereas sclerostin increased (+41.1 pg/mL, P = 0.0001). The remaining bone status indices, lipids, and blood pressure were unchanged. Conclusion: This study suggests that switching to DR-HC leads to lower late-evening cortisol/cortisone exposure and a more favourable metabolic profile and body composition. In contrast, decreased osteocalcin with increasing sclerostin might indicate a negative impact on bones. Clinical trial registration: EudraCT201400203932.",
keywords = "Adrenal insufficiency, Body composition, Diurnal cortisol secretion, Dual-release hydrocortisone, Glucose metabolism",
author = "J{\o}rgensen, {Nanna Thurmann} and Boesen, {Victor Brun} and Borresen, {Stina Willemoes} and Thea Christoffersen and J{\o}rgensen, {Niklas Rye} and Peter Plomgaard and Christina Christoffersen and Torquil Watt and Ulla Feldt-Rasmussen and Marianne Klose",
note = "Publisher Copyright: {\textcopyright} The Author(s) 2024.",
year = "2024",
doi = "10.1007/s12020-024-03711-9",
language = "English",
journal = "Endocrine",
issn = "1355-008X",
publisher = "Humana Press",

}

RIS

TY - JOUR

T1 - Dual-release hydrocortisone improves body composition and the glucometabolic profile in patients with secondary adrenal insufficiency

AU - Jørgensen, Nanna Thurmann

AU - Boesen, Victor Brun

AU - Borresen, Stina Willemoes

AU - Christoffersen, Thea

AU - Jørgensen, Niklas Rye

AU - Plomgaard, Peter

AU - Christoffersen, Christina

AU - Watt, Torquil

AU - Feldt-Rasmussen, Ulla

AU - Klose, Marianne

N1 - Publisher Copyright: © The Author(s) 2024.

PY - 2024

Y1 - 2024

N2 - Purpose: Studies have suggested improved metabolic profiles in patients with adrenal insufficiency treated with dual-release hydrocortisone (DR-HC) compared with conventional hydrocortisone (C-HC). This study investigates the effect of DR-HC compared with C-HC treatment on five health variables: diurnal salivary cortisol/cortisone, body composition, bone health, glucose metabolism, lipids, and blood pressure. Methods: Prospective study of 27 participants (24 men) with secondary adrenal insufficiency with measurements during stable C-HC and 16 weeks after treatment switch to DR-HC. Outcomes: Diurnal salivary-cortisol/cortisone, body composition assessed by Dual-Energy X-ray absorptiometry scan, bone status indices (serum type I N-terminal procollagen [PINP], collagen type I cross-linked C-telopeptide [CTX], osteocalcin, receptor activator kappa-B [RANK] ligand, osteoprotegerin, and sclerostin), lipids, haemoglobin A1c (HbA1c), and 24-hour blood pressure. Results: After the switch to DR-HC, the diurnal salivary-cortisol area under the curve (AUC) decreased non-significantly (mean difference: −55.9 nmol/L/day, P = 0.06). The salivary-cortisone-AUC was unchanged. Late-evening salivary-cortisol and cortisone were lower (−1.6 and −1.7 nmol/L, P = 0.002 and 0.004). Total and abdominal fat mass (−1.5 and −0.5 kg, P = 0.003 and 0.02), HbA1c (−1.2 mmol/mol, P = 0.02), and osteocalcin decreased (−7.0 µg/L, P = 0.03) whereas sclerostin increased (+41.1 pg/mL, P = 0.0001). The remaining bone status indices, lipids, and blood pressure were unchanged. Conclusion: This study suggests that switching to DR-HC leads to lower late-evening cortisol/cortisone exposure and a more favourable metabolic profile and body composition. In contrast, decreased osteocalcin with increasing sclerostin might indicate a negative impact on bones. Clinical trial registration: EudraCT201400203932.

AB - Purpose: Studies have suggested improved metabolic profiles in patients with adrenal insufficiency treated with dual-release hydrocortisone (DR-HC) compared with conventional hydrocortisone (C-HC). This study investigates the effect of DR-HC compared with C-HC treatment on five health variables: diurnal salivary cortisol/cortisone, body composition, bone health, glucose metabolism, lipids, and blood pressure. Methods: Prospective study of 27 participants (24 men) with secondary adrenal insufficiency with measurements during stable C-HC and 16 weeks after treatment switch to DR-HC. Outcomes: Diurnal salivary-cortisol/cortisone, body composition assessed by Dual-Energy X-ray absorptiometry scan, bone status indices (serum type I N-terminal procollagen [PINP], collagen type I cross-linked C-telopeptide [CTX], osteocalcin, receptor activator kappa-B [RANK] ligand, osteoprotegerin, and sclerostin), lipids, haemoglobin A1c (HbA1c), and 24-hour blood pressure. Results: After the switch to DR-HC, the diurnal salivary-cortisol area under the curve (AUC) decreased non-significantly (mean difference: −55.9 nmol/L/day, P = 0.06). The salivary-cortisone-AUC was unchanged. Late-evening salivary-cortisol and cortisone were lower (−1.6 and −1.7 nmol/L, P = 0.002 and 0.004). Total and abdominal fat mass (−1.5 and −0.5 kg, P = 0.003 and 0.02), HbA1c (−1.2 mmol/mol, P = 0.02), and osteocalcin decreased (−7.0 µg/L, P = 0.03) whereas sclerostin increased (+41.1 pg/mL, P = 0.0001). The remaining bone status indices, lipids, and blood pressure were unchanged. Conclusion: This study suggests that switching to DR-HC leads to lower late-evening cortisol/cortisone exposure and a more favourable metabolic profile and body composition. In contrast, decreased osteocalcin with increasing sclerostin might indicate a negative impact on bones. Clinical trial registration: EudraCT201400203932.

KW - Adrenal insufficiency

KW - Body composition

KW - Diurnal cortisol secretion

KW - Dual-release hydrocortisone

KW - Glucose metabolism

U2 - 10.1007/s12020-024-03711-9

DO - 10.1007/s12020-024-03711-9

M3 - Journal article

C2 - 38345683

AN - SCOPUS:85184868515

JO - Endocrine

JF - Endocrine

SN - 1355-008X

ER -

ID: 383709106