Evidence mapPaperPMID 40524210Full record

ReviewDiabetology & metabolic syndrome2025

CARDIAL-MS (CArdio-Renal-DIAbetes-Liver-Metabolic Syndrome): a new proposition for an integrated multisystem metabolic disease.

Amélio F Godoy-Matos, Cynthia Melissa Valério, Wellington S Silva Júnior, João Marcello de Araujo-Neto, Andrei C Sposito, José Hermógenes Rocco Suassuna

Abstract readReview
In one paragraph

Review in Diabetology & metabolic syndrome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Review
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  4. Metabolic dysfunction and the use of adjunct medications in type 1 diabetes.Current opinion in endocrinology, diabetes, and obesity · 2026
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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

6 authors.

Amélio F Godoy-MatosSociedade Brasileira de Diabetes (SBD), São Paulo, Brazil. agodoymatos@gmail.com.ORCID http://orcid.org/0000-0001-9089-9889
Cynthia Melissa ValérioSociedade Brasileira de Diabetes (SBD), São Paulo, Brazil.ORCID http://orcid.org/0000-0003-2292-1735
Wellington S Silva JúniorSociedade Brasileira de Diabetes (SBD), São Paulo, Brazil.ORCID http://orcid.org/0000-0003-4414-6696
João Marcello de Araujo-NetoUniversidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0001-5913-962X
Andrei C SpositoUniversidade Estadual de Campinas (Unicamp), Campinas, SP, Brazil.ORCID http://orcid.org/0000-0001-7127-2052
José Hermógenes Rocco SuassunaUniversidade do Estado do Rio de Janeiro (UERJ), Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-4720-5391

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic Syndrome-a constellation of insulin resistance, cardiovascular risk factors as hyperglycemia, hypertension, and dyslipidemia, and systemic metabolic dysfunction-may be driven by dysregulation of adipose tissue, which manifests as adiposopathy (pathogenic adipose tissue expansion or maldistribution), ectopic fat deposition (in the liver, muscle, pancreas, and cardiorenal systems), and altered secretion of adipokines/hepatokines. Weight gain, obesity, and/or unfavorable fat distribution create a scenario wherein the type, size, location, secretions, or even scarcity of adipocytes drive pathophysiological mechanisms leading to hepatic steatosis and steatohepatitis, type 2 diabetes, and heart and kidney disease. While recent frameworks, such as cardiovascular-kidney-metabolic syndrome, emphasize holistic staging, the central role of metabolic dysfunction-associated steatotic liver disease (MASLD) in multisystem morbidity remains underrecognized. MAIN TEXT: This narrative review synthesizes evidence linking MASLD and diabetes to cardiovascular and kidney diseases through shared pathways of adiposopathy, ectopic lipid accumulation, and dysregulated adipokine/hepatokine signaling. We propose CARDIAL-MS (CArdio-Renal-DIAbetes-Liver-Metabolic Syndrome), an expanded pathophysiological model that unifies these interactions into four progressive stages: (1) weight gain and dysfunctional adipose tissue; (2) metabolic risk factors and markers of risk; (3) cardiometabolic diseases and chronic kidney disease; and (4) advanced cardio-renal-liver-metabolic disease. By integrating MASLD as a pivotal component, CARDIAL-MS reframes metabolic syndrome as a continuum of interconnected organ injuries rather than isolated risk factors.

conclusionCARDIAL-MS provides a staging model to identify patients at critical transition points-from reversible metabolic disturbances to irreversible organ damage. This model emphasizes early interventions targeting adipose tissue health and ectopic fat deposition to mitigate the progression of metabolic cardiorenal diseases. By recognizing the syndromic nature of these conditions, CARDIAL-MS offers clinicians an actionable paradigm for risk stratification, timely diagnosis, and personalized prevention strategies.

Indexed as

AdiposopathyCardiovascular diseaseChronic kidney diseaseEctopic fatMetabolic dysfunction-associated steatotic liver diseaseObesityType 2 diabetes

Identifiers

PMID40524210
PMCPMC12168269

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.