Evidence map›Paper›PMID 42547759›Full record

ReviewGeroScience2026

Targeting the NO-cGMP axis in age-related vascular dysfunction: a systematic review and meta-analysis of preclinical animal studies.

Soroush Mohammadi Jouabadi, Keivan Golshiri, Ehsan Ataei Ataabadi, Youri Boon, Forough Kheiri, Armin Amiri, Mohammad Hosein Khajehali, Arman Amiri, A H Jan Danser, Wichor M Bramer and 2 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in GeroScience, 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

12 authors.

Soroush Mohammadi JouabadiDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands. s.mohammadi@erasmusmc.nl.ORCID http://orcid.org/0000-0002-5710-3057
Keivan GolshiriDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Ehsan Ataei AtaabadiDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Youri BoonDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Forough KheiriDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Armin AmiriDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Mohammad Hosein KhajehaliDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Arman AmiriDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
A H Jan DanserDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Wichor M BramerErasmus Medical Centre, Medical Library, Rotterdam, GD, the Netherlands.
Anton J M RoksDivision of Pharmacology and Vascular Diseases, Department of Internal Medicine, Erasmus MC University Medical Sciences, Rotterdam, The Netherlands.
Carlijn R HooijmansDepartment of Anesthesiology, Pain and Palliative Care, Radboud University Medical Centre, Geert Grooteplein Zuid 10, 6500 HB, Nijmegen, the Netherlands.

Funding

ZonMw 01142042330003ZonMw 01142042330004ZonMw 01142042330006
6 · The paper itself

Abstract

Vascular dysfunction in aging is driven by multiple interconnected hallmarks of aging, including DNA damage, oxidative stress, chronic inflammation, mitochondrial dysfunction, and cellular senescence and features by endothelial impairment, inflammation, and reduced nitric oxide-cyclic guanosine monophosphate (NO-cGMP) signaling. Targeting this pathway may offer therapeutic benefit beyond traditional atherosclerosis-focused treatments. A systematic review and meta-analysis were conducted following PRISMA 2020 guidelines and registered in PROSPERO (CRD42025597982, CRD42025597983, CRD42025598016). PubMed and Embase were systematically searched (August 2024, updated September 2025) for preclinical studies investigating the effect of anti-inflammatory agents (DMARDs), phosphodiesterase (PDE) inhibitors, and soluble guanylate cyclase (sGC) modulators targeting the NO-cGMP pathway in aged animal models of vascular dysfunction. Studies were screened in duplicate using predefined criteria, and data extraction was performed using standardized forms. Risk of bias was assessed using the SYRCLE tool with additional reporting quality items. Meta analyses was conducted using multi-level models accounted for data clustering, and heterogeneity was assessed using I

Indexed as

AgingDMARDsNo-cGMPPDEsSGCsVascular

Identifiers

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.