Evidence map›Paper›PMID 37811017›Full record

ReviewAnnals of medicine and surgery (2012)2023

Efficacy and safety of finerenone in chronic kidney disease and type 2 diabetes patients: a systematic review and meta-analysis.

Farah Yasmin, Muhammad Aamir, Hala Najeeb, Abdul Raafe Atif, Abdul Hannan Siddiqui, Muhammad Nadeem Ahsan, Abdul Moeed, Syed Hasan Ali, Haya Muhammad Tahir, Muhammad Sohaib Asghar

Abstract readReview
In one paragraph

Review in Annals of medicine and surgery (2012), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
–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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Pooled it
  3. Review
  4. Review
  5. 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

10 authors.

Farah YasminDepartment of Internal Medicine, Dow Medical College, Dow University of Health Sciences.
Muhammad AamirDepartment of Cardiovascular Medicine, Lehigh Valley Health Network, Allentown, Pennsylvania.
Hala NajeebDepartment of Internal Medicine, Dow Medical College, Dow University of Health Sciences.
Abdul Raafe AtifDepartment of Internal Medicine, Dow Medical College, Dow University of Health Sciences.
Abdul Hannan SiddiquiDepartment of Internal Medicine, Dow Medical College, Dow University of Health Sciences.
Muhammad Nadeem AhsanDepartment of Nephrology and Dialysis Unit, Dow University of Health Sciences-Ojha Campus, Karachi, Pakistan.
Abdul MoeedDepartment of Internal Medicine, Dow Medical College, Dow University of Health Sciences.
Syed Hasan AliDepartment of Internal Medicine, Dow Medical College, Dow University of Health Sciences.
Haya Muhammad TahirDepartment of Internal Medicine, Jinnah Sindh Medical University.
Muhammad Sohaib AsgharDivision of Nephrology and Hypertension, Mayo Clinic - Rochester, Minnesota, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objectives: The incidence of morbidity and mortality in patients with type 2 diabetes mellitus is substantially correlated with cardiovascular disease and chronic kidney disease. The current guidelines recommend the use of renin-angiotensin system blockers, but recent studies probed into the effects of finerenone to mitigate the risk of cardiorenal events. This meta-analysis was performed to demonstrate the effects of finerenone on cardiorenal events, comprising cardiovascular mortality, heart failure, change in estimated glomerular filtration rate, and serum potassium levels. Methods: After screening with our eligibility criteria, 350 articles were identified with an initial literature search on multiple databases, including PubMed, Science Direct, and Cochrane Central. Seven randomized controlled trials with a total of 15 462 patients ( Results: Patients receiving finerenone were at a reduced risk for cardiovascular mortality [HR: 0.84 (0.74, 0.95)], heart failure [OR: 0.79 (0.68, 0.92)], decrease in estimated glomerular filtration rate by 40% [OR: 0.82 (0.74, 0.91)] and by 57% [OR: 0.70 (0.59, 0.82)]; and a higher incidence of moderate hyperkalemia [OR: 2.25 (1.78, 2.84)]. Conclusion: Finerenone, owing to its better mineralocorticoid affinity, and a much lower risk of adverse effects, promises to be a much better alternative than other renin-angiotensin system blockers available for the treatment of chronic kidney disease patients with type 2 diabetes. Further trials should be conducted to provide more definitive evidence to assess the safety and efficacy of finerenone compared to spironolactone and eplerenone.

Indexed as

chronic kidney disease (CKD)finerenonemeta-analysismineralocorticoid receptor antagnosits (MRA)type 2 diabetes

Identifiers

PMID37811017
PMCPMC10553111

What Socratic holds

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Registered trials

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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.