Evidence map›Paper›PMID 40249765›Full record

Observational studyDiabetes care2025

Prevalence of Hypercortisolism in Difficult-to-Control Type 2 Diabetes.

John B Buse, Steven E Kahn, Vanita R Aroda, Richard J Auchus, Timothy Bailey, Irina Bancos, Robert S Busch, Elena A Christofides, Ralph A DeFronzo, Bradley Eilerman and 17 more

Abstract readObservational Study
In one paragraph

Observational study in Diabetes care, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Trial
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  11. Article
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  14. Review
  15. Review
  16. Article
  17. Article
  18. Breaking Through Difficult-to-Control T2D: Targeting Hypercortisolism.Federal practitioner : for the health care professionals of the VA, DoD, and PHS · 2025
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors.

John B BuseUniversity of North Carolina School of Medicine, Chapel Hill, NC.ORCID 0000-0002-9723-3876
Steven E KahnVA Puget Sound Health Care System and University of Washington, Seattle, WA.ORCID 0000-0001-7307-9002
Vanita R ArodaBrigham and Women's Hospital, Harvard Medical School, Boston, MA.ORCID 0000-0002-7706-4585
Richard J AuchusUniversity of Michigan, Ann Arbor, MI.
Timothy BaileyHeadlands Research AMCR Institute, Escondido, CA.
Irina BancosMayo Clinic, Rochester, MN.
Robert S BuschAlbany Medical College, Community Endocrine Group, Albany, NY.
Elena A ChristofidesEndocrinology Associates, Columbus, OH.ORCID 0000-0002-1595-9906
Ralph A DeFronzoUniversity of Texas Health Science Center at San Antonio, San Antonio, TX.ORCID 0000-0002-8581-6273
Bradley EilermanSt. Elizabeth Physicians, Covington, KY.ORCID 0000-0003-3962-3136
James W FindlingMedical College of Wisconsin, Milwaukee, WI.
Vivian FonsecaTulane University, New Orleans, LA.ORCID 0000-0002-3381-7151
Oksana HamidiUniversity of Texas Southwestern Medical Center, Dallas, TX.
Yehuda HandelsmanMetabolic Institute of America, Tarzana, CA.ORCID 0000-0001-7830-0247
Harold J MillerNOLA Care Clinical Research Center, Covington, LA.
Jonathan G OwnbyAtlanta Diabetes Associates, Atlanta, GA.
John C ParkerAccellacare Research, Wilmington Health, Wilmington, NC.
Athena Philis-TsimikasScripps Whittier Diabetes Institute, Scripps Health, La Jolla, CA.
Richard PratleyAdventHealth Translational Research Institute Orlando, Orlando, FL.
Julio RosenstockVelocity Clinical Research at Medical City Dallas, Dallas, TX.ORCID 0000-0001-8324-3275
Michael H ShanikEndocrine Associates of Long Island, Smithtown, NY.
Lance L SloanTexas Institute for Kidney and Endocrine Disorders, Lufkin, TX.
Guillermo UmpierrezEmory School of Medicine, Emory University, Atlanta, GA.ORCID 0000-0002-3252-5026
Iulia Cristina TudorCorcept Therapeutics Incorporated, Redwood City, CA.
Tina K SchlaflyCorcept Therapeutics Incorporated, Redwood City, CA.ORCID 0009-0006-7769-3046
Daniel EinhornCorcept Therapeutics Incorporated, Redwood City, CA.
CATALYST Investigators*

Funding

Implementing a Maternal health and PRegnancy Outcomes Vision for Everyone (IMPROVE)UL1TR002378 · NCATS · EMORY UNIVERSITY · PI Andres J Garcia, Elizabeth O. Ofili · 2017 to 2026
$92.1M
North Carolina Translational and Clinical Sciences Institute (NC TraCS)UM1TR004406 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NICHOLAS J SHAHEEN · 2023 to 2026
$37.5M
Translational Research Core - Engagement and Behavior ChangeP30DK111024 · NIDDK · EMORY UNIVERSITY · PI Mohammed Kumail Ali · 2016 to 2026
$13.4M
Pilot & Feasibility ProgramP30DK124723 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI P Darrell Neufer · 2020 to 2026
$11.0M
CLC NIH HHSCorcept Therapeutics IncorporatedDiabetes Research Center P30DK124723Diabetes Research Center UM1TR004406NCATS NIH HHS UL1 TR002378NCATS NIH HHS UM1 TR004406NIDDK NIH HHS P30 DK111024NIDDK NIH HHS P30 DK124723U.S. Department of Veterans Affairs
6 · The paper itself

Abstract

objectiveDespite the use of multiple glucose-lowering medications, glycemic targets are not met in a significant fraction of people with type 2 diabetes. In this prospective, observational study we assessed the prevalence of hypercortisolism, a potential contributing factor to inadequate glucose control. RESEARCH DESIGN AND

methodsIndividuals with type 2 diabetes and HbA1c 7.5%-11.5% (58-102 mmol/mol) on two or more glucose-lowering medications with or without micro-/macrovascular complications or taking multiple blood pressure-lowering medications were screened with a 1-mg dexamethasone suppression test. Common causes of false-positive DSTs were excluded. The primary end point was the prevalence of hypercortisolism, defined as post-DST cortisol >1.8 μg/dL (50 nmol/L). Characteristics associated with hypercortisolism were assessed with multiple logistic regression. The percentage and characteristics of participants with hypercortisolism and adrenal imaging abnormalities were also assessed.

resultsPost-DST cortisol was unsuppressed in 252 of 1,057 participants (prevalence 23.8%; 95% CI 21.3, 26.5). Hypercortisolism prevalence was 33.3% among participants with cardiac disorders and 36.6% among those taking three or more blood pressure-lowering medications. Adrenal imaging abnormalities were reported in 34.7% of participants with hypercortisolism. Use of sodium-glucose cotransporter 2 inhibitors (odds ratio 1.558), maximum-dose glucagon-like peptide 1 receptor agonists (1.544), tirzepatide (1.981), or a higher number of blood pressure-lowering medications (1.390); older age (1.316); BMI <30 kg/m2 (1.639); non-Latino/Hispanic ethnicity (3.718); and use of fibrates (2.676) or analgesics (1.457) were associated with higher prevalence (all P < 0.03).

conclusionsHypercortisolism was associated with hyperglycemia in approximately one-quarter of individuals with inadequately controlled type 2 diabetes despite multiple medications.

Indexed as

Cushing SyndromeDiabetes Mellitus, Type 2AgedFemaleHumansHydrocortisoneHypoglycemic AgentsMaleMiddle AgedPrevalenceProspective StudiesHydrocortisoneHypoglycemic Agents

Identifiers

PMID40249765
PMCPMC12635953

What OpenQuestion holds

Textmetadata
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.