Evidence map›Paper›PMID 37831346›Full record

ArticleMolecular biology reports2023

Circulating hsa-miR-221 as a possible diagnostic and prognostic biomarker of diabetic nephropathy.

Marwa Sayed Abdel-Tawab, Mohamed Gamal Mohamed, Noha A Doudar, Enas Ezzat Rateb, Hoda Ramadan Reyad, Naglaa Adli Abd Elazeem

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Noncoding RNAs and diabetic kidney disease.Journal of diabetes investigation · 2025
    Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Marwa Sayed Abdel-TawabMedical Biochemistry Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt. drmarwasayed2016@gmail.com.
Mohamed Gamal MohamedInternal Medicine Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Noha A DoudarClinical and Chemical Pathology Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Enas Ezzat RatebPhysiology Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Hoda Ramadan ReyadMedical Biochemistry Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Naglaa Adli Abd ElazeemMedical Biochemistry Department, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt.
Beni-Suef University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic nephropathy (DN), which is a chronic outcome of diabetes mellitus (DM), usually progresses to end-stage renal disease (ESRD). The DN pathophysiology, nevertheless, is not well-defined. Several miRNAs were reported to be either risk or protective factors in DN. METHODS, AND

resultsThe present study sought to inspect the potential diagnostic and prognostic value of hsa-miR-221 in DN. The study included 200 participants divided into four groups: Group 1 (50 patients with DN), Group 2 (50 diabetic patients without nephropathy), Group 3 (50 nondiabetic patients with CKD), and Group 4 (50 healthy subjects as a control group). Patients in groups 1 and 3 were further classified based on the presence of macroalbuminuria and microalbuminuria. Hsa-miR-221 expression was measured by RT- qRT-PCR. DN patients had significantly elevated serum hsa-miR-221 levels than the other groups, while diabetic patients without nephropathy exhibited elevated levels compared to both nondiabetic patients with CKD, and the control group. The DN patients with macroalbuminuria revealed significantly higher mean values of hsa-miR-221 relative to the patients with microalbuminuria. Significant positive associations were observed in the DN group between serum hsa-miR-221 and fasting insulin, fasting glucose, HOMA IR, ACR, and BMI. The ROC curve analysis of serum hsa-miR-221 in the initial diagnosis of DN in DM revealed high specificity and sensitivity.

conclusionsIt is concluded that hsa-miR-221 has the potential to be a useful biomarker for prognostic and diagnostic purposes in DN.

Indexed as

Diabetes Mellitus, Type 2Diabetic NephropathiesMicroRNAsRenal Insufficiency, ChronicAlbuminuriaBiomarkersHumansPrognosisBiomarkersMicroRNAsMIR221, humanDiabetes mellitusDiabetic nephropathyhsa-miR-221

Identifiers

PMID37831346
PMCPMC10676308
OpenAlexW4387599607

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.