Evidence map›Paper›PMID 27999645›Full record

ArticleCaspian journal of internal medicine2016

Serum alpha-actinin antibody status in systemic lupus erythematosus and its potential in the diagnosis of lupus nephritis.

Mansour Babaei, Zahra Rezaieyazdi, Nayereh Saadati, Massoud Saghafi, Maryam Sahebari, Bahram Naghibzadeh, Habibollah Esmaily

Open access · greenAbstract read
In one paragraph

Article in Caspian journal of internal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Lupus Nephritis Biomarkers: A Critical Review.International journal of molecular sciences · 2024
    Review
  2. Review
  3. Utilization of Biomarkers in Lupus Nephritis.Advances in chronic kidney disease · 2019
    Review
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

7 authors at 2 institutions in 1 country.

Mansour BabaeiDepartment of Rheumatology, Ayatollah Rouhani Hospital, Babol University of Medical Sciences, Babol, Iran.
Zahra RezaieyazdiRheumatic Disease Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Nayereh SaadatiRheumatic Disease Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Massoud SaghafiRheumatic Disease Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Maryam SahebariRheumatic Disease Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Bahram NaghibzadehCenter for Health Sciences Research, School of Health, Mashhad University of Medical Sciences, Mashhad, Iran.
Habibollah EsmailyCenter for Health Sciences Research, School of Health, Mashhad University of Medical Sciences, Mashhad, Iran.
Mashhad University of Medical Sciences · IRBabol University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn lupus nephritis (LN), deposition of pathogenic autoantibodies in the glomeruli is mediated via cross-reactivity with alpha-actinin. Association of serum alpha-actinin antibody (AαA) with LN has been shown in a few studies but the results are controversial.

methodsEighty patients into entered the study. The diagnosis of SLE was confirmed according to the American College of Rheumatology criteria and LN was diagnosed by proteinuria ≥ 500 mg/24 hour and kidney biopsy. Serum AαA was measured with ELISA method. Receiver operating characteristics curve (ROC) analysis was applied to determine an optimal cutoff value for AαA to discriminate patients with and without LN at the highest sensitivity and specificity. The association of AαA with LN was determined by logistic regression analysis with calculation of odds ratio (OR).

resultsSerum AαA was significantly lower in LN as compared with SLE patients without LN (P=0.001). Serum AαA at cutoff levels ≤ 59.5 pg/ml discriminated the two groups with sensitivity, specificity, positive predictive values of 60%. 90% and 85.7%, respectively. Serum AαA level ≤ 59.5 pg/ml was significantly associated with LN (OR=13.5, P=0.001) and the OR increased to 25.2 (P=0.003) after adjustment for age, sex, C3, C4, anti-ds-DNA, SLEDAI.

conclusionThis study indicates that serum AαA decreases in LN and serum level ≤ 59.5 pg/ml is SLE and is predictive of nephritis.

Indexed as

Anti-alpha-actinicn antibodyDiagnosis.NephritisSystemic lupus erythematous

Identifiers

PMID27999645
PMCPMC5153519
OpenAlexW2585760866

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.