Evidence map›Paper›PMID 37147676›Full record

ArticleOrphanet journal of rare diseases2023

Hepatic fibrosis: a manifestation of the liver disease evolution in patients with Ataxia-telangiectasia.

Talita Lemos Neves Barreto, Roberto José de Carvalho Filho, David Carlos Shigueoka, Fernando Luiz Affonso Fonseca, Ariel Cordeiro Ferreira, Cristiane Kochi, Carolina Sanchez Aranda, Roseli Oselka Saccardo Sarni

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

Talita Lemos Neves BarretoDepartment of Pediatrics, Division of Allergy, Clinical Immunology and Rheumatology, Universidade Federal de São Paulo (UNIFESP), 731 Otonis St., Vila Clementino, São Paulo, SP, Brazil. talita.lemos@unifesp.br.ORCID 0000-0001-5440-4615
Roberto José de Carvalho FilhoDepartment of Gastroenterology, Universidade Federal de São Paulo (UNIFESP), 1570 Loefgren St., Vila Clementino, São Paulo, SP, Brazil.
David Carlos ShigueokaDepartment of Diagnostic Imaging, Universidade Federal de São Paulo (UNIFESP), 800 Napoleão de Barros St., Vila Clmementino, São Paulo, SP, Brazil.
Fernando Luiz Affonso FonsecaCentro Universitário FMABC, 821 Príncipe de Gales Av., Santo André, SP, Brazil.
Ariel Cordeiro FerreiraCentro Universitário FMABC, 821 Príncipe de Gales Av., Santo André, SP, Brazil.
Cristiane KochiFaculdade de Ciências Médicas da Santa Casa de São Paulo (FCMSCSP), 61 Dr. Cesário Motta Jr. St., São Paulo, SP, Brazil.
Carolina Sanchez ArandaDepartment of Pediatrics, Division of Allergy, Clinical Immunology and Rheumatology, Universidade Federal de São Paulo (UNIFESP), 731 Otonis St., Vila Clementino, São Paulo, SP, Brazil.
Roseli Oselka Saccardo SarniDepartment of Pediatrics, Division of Allergy, Clinical Immunology and Rheumatology, Universidade Federal de São Paulo (UNIFESP), 731 Otonis St., Vila Clementino, São Paulo, SP, Brazil.
Faculdade de Medicina do ABC · BRUniversidade Federal de São Paulo · BRFaculdade de Ciências Médicas da Santa Casa de São Paulo · BRFundação de Apoio à Universidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtaxia-telangiectasia (A-T) is a DNA repair disorder characterized by changes in several organs and systems. Advances in clinical protocols have resulted in increased survival of A-T patients, however disease progression is evident, mainly through metabolic and liver changes.

objectiveTo identify the frequency of significant hepatic fibrosis in A-T patients and to verify the association with metabolic alterations and degree of ataxia.

methodsThis is a cross-sectional study that included 25 A-T patients aged 5 to 31 years. Anthropometric data, liver, inflammatory, lipid metabolism and glucose biomarkers (oral glucose tolerance test with insulin curve-OGTT) were collected. The Cooperative Ataxia Rating Scale was applied to assess the degree of ataxia. The following were calculated: Homeostasis Model Assessment-Insulin Resistance, Homeostasis Model Assessment-Adiponectin (HOMA-AD), Matsuda index, aspartate aminotransferase (AST): platelet ratio index, nonalcoholic fatty liver disease fibrosis score and BARD score. Liver ultrasonography and transient liver elastography by FibroScan

resultsSignificant hepatic fibrosis was observed in 5/25 (20%). Patients in the group with significant hepatic fibrosis were older (p < 0.001), had lower platelet count values (p = 0.027), serum albumin (p = 0.019), HDL-c (p = 0.013) and Matsuda index (p = 0.044); and high values of LDL-c (p = 0.049), AST (p = 0.001), alanine aminotransferase (p = 0.002), gamma-glutamyl transferase (p = 0.001), ferritin (p = 0.001), 120-min glycemia by OGTT (p = 0.049), HOMA-AD (p = 0.016) and degree of ataxia (p = 0.009).

conclusionsA non-invasive diagnosis of significant hepatic fibrosis was observed in 20% of A-T patients associated with changes in liver enzymes, ferritin, increased HOMA-AD, and the severity of ataxia in comparison with patients without hepatic fibrosis.

Indexed as

Ataxia TelangiectasiaInsulin ResistanceNon-alcoholic Fatty Liver DiseaseCross-Sectional StudiesHumansLiverLiver CirrhosisAtaxia-telangiectasiaHepatic fibrosisImage techniques by elasticityInflammationInsulin resistance

Identifiers

PMID37147676
PMCPMC10161655
OpenAlexW4372336062

What OpenQuestion holds

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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.