Evidence map›Paper›PMID 39726840›Full record

ArticleFrontiers in endocrinology2024

Mild autonomous cortisol secretion leads to reduced volumetric BMD at lumbar spine in patients with primary aldosteronism.

Nabeel Mansour, Denise Bruedgam, Daniel Heinrich, Ulrich Dischinger, Nicole Reisch, Friederike Völter, Isabel Stüfchen, Elisabeth Nowak, Stephanie Zopp, Victoriya Vasileva and 7 more

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Nabeel MansourDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.
Denise BruedgamDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Daniel HeinrichDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Ulrich DischingerDepartment of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital, University of Würzburg, Würzburg, Germany.
Nicole ReischDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Friederike VölterDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Isabel StüfchenDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Elisabeth NowakDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Stephanie ZoppDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Victoriya VasilevaDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.
Osman ÖcalDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.
Moritz WildgruberDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.
Max SeidenstickerDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.
Jens RickeDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.
Martin BidlingmaierDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Martin ReinckeDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.
Juínia Ribeiro de Oliveira Longo SchweizerDepartment of Medicine IV, LMU University Hospital, LMU Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Glucocorticoid cosecretion is more common in primary aldosteronism (PA) than previously thought. Chronic subtle cortisol excess in patients with mild autonomous cortisol secretion (MACS) negatively affects bone health. This study aimed to evaluate the impact of MACS on bone density and turnover markers in PA patients. Methods: Patients with PA and MACS (n = 50), confirmed by a 1-mg dexamethasone suppression test (DST) with a cortisol cutoff of ≥1.8 µg/dL without symptoms of overt Cushing, were compared to age- and sex-matched patients with PA without MACS (non-MACS, n = 50). Lumbar volumetric bone mineral density (vBMD) was extracted by a novel convolutional neural network (CNN)-based framework (SpineQ software v1.0) applied to routine CT data, incorporated into the diagnostic protocol for PA. Additionally, bone turnover markers-including osteocalcin, bone-specific alkaline phosphatase, N-terminal propeptide of type I collagen, and carboxy-terminal crosslinked telopeptide of type I collagen were evaluated between the groups. Results: Median cortisol after DST was 1.1 µg/dL (30.3 nmol/L) [IQR: 0.5 µg/dL (13.8 nmol/L)] in the non-MACS group and 2.5 µg/dL (69.0 nmol/L) [IQR: 1.4 µg/dL (38.5 nmol/L)] in the MACS group (p < 0.001). Patients with MACS had significantly lower vBMD values compared to the non-MACS group (106.4 mg/cm³ vs. 116.6 mg/cm³, p = 0.038). Cortisol after DST negatively correlated with vBMD (Spearman's r=-0.33, p=0.00042). No significant differences in bone turnover markers were found, and classifications based on visible lesions on CT or PA-lateralization via adrenal venous sampling did not reveal any significant differences in these markers (p > 0.05 for all comparisons). Conclusion: Despite non-significant differences in bone turnover markers between patients with PA with or without MACS, CT scans revealed significantly reduced vBMD in PA and MACS patients, indicating compromised bone health and vBMD significantly negatively correlated with cortisol post DST. Thus, opportunistic evaluation of vBMD in routine CT screenings could aid in the early detection of bone alterations in MACS and help mitigate potential long-term adverse effects on bone health.

Indexed as

Bone DensityHydrocortisoneHyperaldosteronismLumbar VertebraeAdultAgedBiomarkersBone RemodelingFemaleHumansMaleMiddle AgedBiomarkersHydrocortisoneACTHbone turnover markersConn’s syndromecortisolMACsprimary aldosteronismvolumetric bone mineral density

Identifiers

PMID39726840
PMCPMC11669511

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.