Evidence map›Paper›PMID 37638982›Full record

ArticlePediatric nephrology (Berlin, Germany)2024

Kidney manifestations of pediatric Sjögren's syndrome.

Saverio La Bella, Marina Vivarelli, Armando Di Ludovico, Giulia Di Donato, Francesco Chiarelli, Luciana Breda

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Renal disease in pediatric rheumatology.Current opinion in rheumatology · 2024
    Review
  9. Article
  10. Article
  11. 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

6 authors at 2 institutions in 1 country.

Saverio La BellaDepartment of Pediatrics, University "G. D'Annunzio" of Chieti-Pescara, Chieti, Italy. saverio.labella@studenti.unich.it.ORCID 0000-0002-1244-0789
Marina VivarelliDivision of Nephrology, Laboratory of Nephrology, Bambino Gesù Children's Hospital IRCCS, Rome, Italy.
Armando Di LudovicoDepartment of Pediatrics, University "G. D'Annunzio" of Chieti-Pescara, Chieti, Italy.
Giulia Di DonatoDepartment of Pediatrics, University "G. D'Annunzio" of Chieti-Pescara, Chieti, Italy.
Francesco ChiarelliDepartment of Pediatrics, University "G. D'Annunzio" of Chieti-Pescara, Chieti, Italy.
Luciana BredaDepartment of Pediatrics, University "G. D'Annunzio" of Chieti-Pescara, Chieti, Italy.
University of Chieti-Pescara · ITBambino Gesù Children's Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately 1% of all patients with Sjögren's syndrome (SS) are children. Unlike the adult form, in which sicca syndrome is the main presentation, in children, the most common clinical finding is recurrent enlargement of the salivary glands. In pediatric SS, extraglandular manifestations represent a significant feature and, among these, kidney manifestations are relevant. Kidney involvement is observed in 5-20.5% of children with SS, most frequently tubulointerstitial nephritis. This injury can lead to serious phenotypes, including distal kidney tubular acidosis with the development of severe hypokalemia, which can lead to ECG abnormalities, weakness, and hypokalemic periodic paralysis. Kidney implications in pediatric SS also include nephrolithiasis, nephrocalcinosis, and various types of glomerular damage, which often require immunosuppressive therapies. Laboratory findings are usually comparable to adults, including hyperglobulinemia and high rates of antinuclear antibodies (ANA, 63.6-96.2%), and anti-Ro/SSA (36.4-84.6%). The current classification criteria for SS are inaccurate for the pediatric population, and more specific criteria are needed to improve the diagnostic rate. Due to the rarity of the disease, strong recommendations for treatment are lacking, and several therapeutic strategies have been reported, mostly based on glucocorticoids and disease-modifying antirheumatic drugs, with different outcomes. The aim of this paper is to provide an overview of the kidney implications of pediatric SS based on the latest evidence of the medical literature.

Indexed as

Acidosis, Renal TubularHypokalemiaNephritis, InterstitialSjogren's SyndromeAdultChildHumansKidneyKidneyPediatric Sjögren’s syndromePrimary Sjogren’s syndromeRenalTubulointerstitial nephritis

Identifiers

PMID37638982
OpenAlexW4386208837

What OpenQuestion 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 OpenQuestion graph.