Cargando…

THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study

Disclosure: C.D. Zhang: None. S. Singh: None. J. Saini: None. M. Suresh: None. K. Thangamuthu: None. R. Nathani: None. A.L. Ebbehøj: None. V. Fell: None. S.J. Achenbach: None. E.J. Atkinson: None. S. Khosla: None. I. Bancos: None. Background: Patients with mild autonomous cortisol secretion (MACS) h...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Catherine D, Singh, Sumitabh, Saini, Jasmine, Suresh, Malavika, Thangamuthu, Karthik, Nathani, Rohit, Ebbehøj, Andreas Ladefoged, Fell, Vanessa, Achenbach, Sara J, Atkinson, Elizabeth J, Khosla, Sundeep, Bancos, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554138/
http://dx.doi.org/10.1210/jendso/bvad114.133
_version_ 1785116340965605376
author Zhang, Catherine D
Singh, Sumitabh
Saini, Jasmine
Suresh, Malavika
Thangamuthu, Karthik
Nathani, Rohit
Ebbehøj, Andreas Ladefoged
Fell, Vanessa
Achenbach, Sara J
Atkinson, Elizabeth J
Khosla, Sundeep
Bancos, Irina
author_facet Zhang, Catherine D
Singh, Sumitabh
Saini, Jasmine
Suresh, Malavika
Thangamuthu, Karthik
Nathani, Rohit
Ebbehøj, Andreas Ladefoged
Fell, Vanessa
Achenbach, Sara J
Atkinson, Elizabeth J
Khosla, Sundeep
Bancos, Irina
author_sort Zhang, Catherine D
collection PubMed
description Disclosure: C.D. Zhang: None. S. Singh: None. J. Saini: None. M. Suresh: None. K. Thangamuthu: None. R. Nathani: None. A.L. Ebbehøj: None. V. Fell: None. S.J. Achenbach: None. E.J. Atkinson: None. S. Khosla: None. I. Bancos: None. Background: Patients with mild autonomous cortisol secretion (MACS) have higher rates of fractures compared to patients with non-functioning adrenal nodules, but bone mass is typically only modestly reduced. We hypothesized that chronic exposure to mild levels of cortisol excess may lead to a deterioration in bone quality. Objective: To characterize the effect of MACS on bone metabolism and bone microarchitecture, as measured by high-resolution peripheral quantitative computed tomography (HR-pQCT). Methods: In this cross-sectional single-center study, patients with MACS were matched by age, sex, and gonadal status to referent subjects without adrenal nodules. MACS was defined as serum cortisol concentration >1.8 mcg/dL after the 1 mg overnight dexamethasone suppression test (1-mg DST), in the absence of a classic Cushingoid phenotype. Those with other known secondary causes of osteoporosis and/or on pharmacologic treatment for low bone mass were excluded. All study participants underwent a bone health interview, blood draw for bone turnover markers, dual-energy x-ray absorptiometry (DXA) scan with trabecular bone score (TBS), and HR-pQCT of the non-dominant radius and tibia. Participants with a recent fracture within 12 months were excluded from the analysis of bone turnover markers. The Kruskal-Wallis test was used to compare measurements between groups. Results: A total of 82 patients with MACS and 82 referent subjects were prospectively enrolled between 1/2019 and 7/2022. The median age of study participants at the time of enrolment was 57 years (interquartile range [IQR], 47-65), and 57 (70%) were women. In the MACS cohort, the median cortisol following 1-mg DST was 3.2 mcg/dL (IQR, 2.3-6.5) with median ACTH of 8.7 pg/mL (IQR, 6.0-14.0) and median DHEA-S of 42.0 mcg/dL (IQR 23.0-68.0). While no differences in bone mineral density (BMD) were observed at any site (lumbar spine, total hip, femoral neck, or distal radius) between the two groups, patients with MACS had decreased TBS (1.374 vs 1.467, P <0.001) and lower osteocalcin concentrations (16.9 vs. 19.7 ng/mL, P = 0.005) than referent subjects without adrenal nodules. On HR-pQCT at the tibia, patients with MACS had significantly reduced trabecular volumetric BMD (151.6 vs 167.4 mg hydroxyapatite/cm(3), P = 0.002), trabecular bone volume/tissue volume ratio (0.219 vs 0.237, P = 0.011), and number of trabeculae (1.428 vs 1.506 1/mm, P = 0.045), while trabecular separation (0.707 vs 0.656, P = 0.023) was increased compared to referent subjects. Conclusions: Patients with MACS have altered bone metabolism and microstructural deterioration that is not evident on routine DXA BMD testing. These changes may mediate their increased fracture risk and could serve as biomarkers of cortisol-induced changes in the bone. Presentation: Thursday, June 15, 2023
format Online
Article
Text
id pubmed-10554138
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-105541382023-10-06 THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study Zhang, Catherine D Singh, Sumitabh Saini, Jasmine Suresh, Malavika Thangamuthu, Karthik Nathani, Rohit Ebbehøj, Andreas Ladefoged Fell, Vanessa Achenbach, Sara J Atkinson, Elizabeth J Khosla, Sundeep Bancos, Irina J Endocr Soc Adrenal (Excluding Mineralocorticoids) Disclosure: C.D. Zhang: None. S. Singh: None. J. Saini: None. M. Suresh: None. K. Thangamuthu: None. R. Nathani: None. A.L. Ebbehøj: None. V. Fell: None. S.J. Achenbach: None. E.J. Atkinson: None. S. Khosla: None. I. Bancos: None. Background: Patients with mild autonomous cortisol secretion (MACS) have higher rates of fractures compared to patients with non-functioning adrenal nodules, but bone mass is typically only modestly reduced. We hypothesized that chronic exposure to mild levels of cortisol excess may lead to a deterioration in bone quality. Objective: To characterize the effect of MACS on bone metabolism and bone microarchitecture, as measured by high-resolution peripheral quantitative computed tomography (HR-pQCT). Methods: In this cross-sectional single-center study, patients with MACS were matched by age, sex, and gonadal status to referent subjects without adrenal nodules. MACS was defined as serum cortisol concentration >1.8 mcg/dL after the 1 mg overnight dexamethasone suppression test (1-mg DST), in the absence of a classic Cushingoid phenotype. Those with other known secondary causes of osteoporosis and/or on pharmacologic treatment for low bone mass were excluded. All study participants underwent a bone health interview, blood draw for bone turnover markers, dual-energy x-ray absorptiometry (DXA) scan with trabecular bone score (TBS), and HR-pQCT of the non-dominant radius and tibia. Participants with a recent fracture within 12 months were excluded from the analysis of bone turnover markers. The Kruskal-Wallis test was used to compare measurements between groups. Results: A total of 82 patients with MACS and 82 referent subjects were prospectively enrolled between 1/2019 and 7/2022. The median age of study participants at the time of enrolment was 57 years (interquartile range [IQR], 47-65), and 57 (70%) were women. In the MACS cohort, the median cortisol following 1-mg DST was 3.2 mcg/dL (IQR, 2.3-6.5) with median ACTH of 8.7 pg/mL (IQR, 6.0-14.0) and median DHEA-S of 42.0 mcg/dL (IQR 23.0-68.0). While no differences in bone mineral density (BMD) were observed at any site (lumbar spine, total hip, femoral neck, or distal radius) between the two groups, patients with MACS had decreased TBS (1.374 vs 1.467, P <0.001) and lower osteocalcin concentrations (16.9 vs. 19.7 ng/mL, P = 0.005) than referent subjects without adrenal nodules. On HR-pQCT at the tibia, patients with MACS had significantly reduced trabecular volumetric BMD (151.6 vs 167.4 mg hydroxyapatite/cm(3), P = 0.002), trabecular bone volume/tissue volume ratio (0.219 vs 0.237, P = 0.011), and number of trabeculae (1.428 vs 1.506 1/mm, P = 0.045), while trabecular separation (0.707 vs 0.656, P = 0.023) was increased compared to referent subjects. Conclusions: Patients with MACS have altered bone metabolism and microstructural deterioration that is not evident on routine DXA BMD testing. These changes may mediate their increased fracture risk and could serve as biomarkers of cortisol-induced changes in the bone. Presentation: Thursday, June 15, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10554138/ http://dx.doi.org/10.1210/jendso/bvad114.133 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Adrenal (Excluding Mineralocorticoids)
Zhang, Catherine D
Singh, Sumitabh
Saini, Jasmine
Suresh, Malavika
Thangamuthu, Karthik
Nathani, Rohit
Ebbehøj, Andreas Ladefoged
Fell, Vanessa
Achenbach, Sara J
Atkinson, Elizabeth J
Khosla, Sundeep
Bancos, Irina
THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study
title THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study
title_full THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study
title_fullStr THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study
title_full_unstemmed THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study
title_short THU603 Bone Fragility In Mild Autonomous Cortisol Secretion: A Cross-Sectional Cohort Study
title_sort thu603 bone fragility in mild autonomous cortisol secretion: a cross-sectional cohort study
topic Adrenal (Excluding Mineralocorticoids)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554138/
http://dx.doi.org/10.1210/jendso/bvad114.133
work_keys_str_mv AT zhangcatherined thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT singhsumitabh thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT sainijasmine thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT sureshmalavika thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT thangamuthukarthik thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT nathanirohit thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT ebbehøjandreasladefoged thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT fellvanessa thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT achenbachsaraj thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT atkinsonelizabethj thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT khoslasundeep thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy
AT bancosirina thu603bonefragilityinmildautonomouscortisolsecretionacrosssectionalcohortstudy