Evidence map›Paper›PMID 42735200›Full record

ReviewMedical science monitor : international medical journal of experimental and clinical research2026

Selective Glucocorticoid Receptor Modulators (SEGRAMs): Can They Improve the Therapeutic Index of Steroid Therapy?

Michał Pruc, Basar Cander, Iwona Jannasz, Zbigniew Siudak, Konrad Kubiński, Karol Momot, Artur Mamcarz, Queran Lin, Łukasz Szarpak

Abstract readReview
In one paragraph

Review in Medical science monitor : international medical journal of experimental and clinical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Michał PrucInstitute of Medical Sciences, The John Paul Catholic University of Lublin, Lublin, Poland.ORCID 0000-0002-2140-9732
Basar CanderDepartment of Emergency Medicine, Bezmialem Vakif University, Istanbul, Turkey.
Iwona JannaszDepartment of Geriatrics, National Institute of Geriatrics, Rheumatology and Rehabilitation, Warsaw, Poland.
Zbigniew SiudakCollegium Medicum, Jan Kochanowski University, Kielce, Poland.ORCID 0000-0002-8033-3977
Konrad KubińskiInstitute of Biological Sciences, The John Paul Catholic University of Lublin, Lublin, Poland.ORCID 0000-0001-6870-845X
Karol MomotDepartment of Experimental and Clinical Physiology, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0001-8659-2948
Artur Mamcarz3rd Department of Internal Diseases and Cardiology, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0002-9569-1486
Queran LinDepartment of Primary Care & Public Health, Faculty of Medicine, School of Public Health, WHO Collaborating Centre, Imperial College London, London, United Kingdom.
Łukasz SzarpakInstitute of Medical Sciences, The John Paul Catholic University of Lublin, Lublin, Poland.ORCID 0000-0002-0973-5455

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucocorticoids remain indispensable anti-inflammatory drugs across a wide range of inflammatory and immune-mediated diseases, but their long-term use is limited by cumulative toxicity. Attempts to develop safer steroids gave rise to selective glucocorticoid receptor agonists and modulators (SEGRAMs), initially based on the premise that anti-inflammatory efficacy might be preserved while signaling linked to adverse effects was reduced. Current glucocorticoid receptor biology no longer supports such a simple binary model. Glucocorticoid receptor output is shaped by ligand-induced conformation, DNA sequence, chromatin accessibility, cofactor recruitment, and cell-specific transcriptional context, making selective modulation a context-dependent pharmacologic phenomenon rather than a fixed molecular property. In this clinically oriented narrative review, we reassess the SEGRAMs concept from receptor biology to translational and early clinical evidence, with explicit distinction between mechanistic dissociation, translational separation of efficacy from selected toxicities, and clinically meaningful improvement in the therapeutic index. Representative compounds have shown that selective glucocorticoid receptor modulation is pharmacologically feasible and, in some settings, may separate anti-inflammatory activity from selected steroid-related liabilities. However, the available evidence also indicates that any potential advantage is disease-specific, toxicity-specific, and exposure-dependent, and that mechanistic dissociation does not by itself justify therapeutic claims, particularly in the absence of long-term comparative outcome data. The most credible future for SEGRAMs lies not in universal replacement of conventional glucocorticoids, but in their potential to improve the therapeutic index in diseases for which prolonged or repeated glucocorticoid exposure remains necessary, but in which cumulative harm from toxicity is a major treatment burden.

Indexed as

GlucocorticoidsReceptors, GlucocorticoidSteroidsAnimalsAnti-Inflammatory AgentsHumansInflammationSignal TransductionAnti-Inflammatory AgentsGlucocorticoidsReceptors, GlucocorticoidSteroids

Identifiers

PMID42735200
PMCPMC13587748

What Socratic 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 Socratic graph.