Evidence map›Paper›PMID 26095468›Full record

ArticleClinical and experimental immunology2015

C1q rs292001 polymorphism and C1q antibodies in juvenile lupus and their relation to lupus nephritis.

Y M Mosaad, A Hammad, Z Fawzy, A El-Refaaey, Z Tawhid, E M Hammad, L F Youssef, E A A ElAttar, D F Radwan, I M Fawzy

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. [Correlation of anti-C1q antibodies with active systemic lupus erythematosus and lupus nephritis in children].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2024
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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

10 authors at 3 institutions in 1 country.

Y M MosaadClinical Immunology Unit, Clinical Pathology Department and Mansoura Research Center for Cord Stem Cells (MARC_CSC), Faculty of Medicine, Mansoura University, Mansoura, Egypt.
A HammadPediatric Nephrology Unit, Mansoura University Children's Hospital, Mansoura, Egypt.
Z FawzyClinical Immunology Unit, Clinical Pathology Department and Mansoura Research Center for Cord Stem Cells (MARC_CSC), Faculty of Medicine, Mansoura University, Mansoura, Egypt.
A El-RefaaeyPediatric Nephrology Unit, Mansoura University Children's Hospital, Mansoura, Egypt.
Z TawhidClinical Immunology Unit, Clinical Pathology Department and Mansoura Research Center for Cord Stem Cells (MARC_CSC), Faculty of Medicine, Mansoura University, Mansoura, Egypt.
E M HammadRheumatology and Rehabilitation Department, Mansoura University Hospital, Mansoura, Egypt.
L F YoussefDepartment of Biochemistry, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
E A A ElAttarPediatric Department, Mansoura General Hospital, Mansoura, Egypt.
D F RadwanBlood Bank, Central Talkha Hospital, Mansoura, Egypt.
I M FawzyLaboratory Medicine Department, Mansoura Fever Hospital, Ministry of Health, Mansoura, Egypt.
Mansoura University · EGMansoura University Hospital · EGChildren's Hospital Mansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

C1q deficiency is related strongly to systemic lupus erythematosus (SLE), but very few and inconsistent studies explored the single nucleotide polymorphisms of the C1q gene in relation to juvenile SLE (jSLE) and lupus nephritis (LN). The objective of this study was to analyse whether C1q rs 292001 polymorphism is associated with SLE and disease phenotype, especially nephritis, and to investigate the relation between this polymorphism and clinical data, treatment outcome, serum level of C1q protein and antibodies. Typing of C1q rs292001 polymorphism using restriction fragment length polymorphism and measuring serum levels of C1q protein and antibodies by enzyme-linked immunosorbent assay (ELISA) were performed for 130 children with SLE and 208 healthy controls. The A allele of C1q rs292001 was associated with jSLE and LN (P = 0·005 and 0·013, respectively) and the AA genotype was associated with jSLE (P = 0·036). Low serum levels of C1q protein were found in jSLE and LN (P < 0·001 and 0·009, respectively), and these levels were increased after treatment in patients with LN (P = 0·009) and active renal disease (P = 0·027). Higher titres of C1q antibodies were found in patients with LN (P = 0·015) and correlated negatively with C1q protein level (P < 0·001) and patient age (P = 0·04). The A allele and AA genotype of C1q rs292001 can be considered a susceptibility risk factor and the GG genotype could be considered protective for jSLE and LN in the studied cohort of Egyptian children. Decreased serum levels of C1q protein and increased titres of C1q antibodies may be involved in the pathogenesis of jSLE, especially LN.

Indexed as

AutoantibodiesChildComplement C1qEgyptEnzyme-Linked Immunosorbent AssayFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansLupus NephritisMalePolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideSeverity of Illness IndexTreatment OutcomeAutoantibodiesComplement C1qautoantibodyC1qEgyptianjuvenilenephritispolymorphismserum

Identifiers

PMID26095468
PMCPMC4578505
OpenAlexW1889240260

What OpenQuestion holds

Textmetadata
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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 OpenQuestion graph.