Evidence map›Paper›PMID 39085658›Full record

ArticleEuropean journal of pediatrics2024

Exploring factors for predicting colchicine responsiveness in children with PFAPA.

Zeynep Özaslan, Abdulvahap Şen, Sıla Atamyıldız Uçar, Mustafa Çakan, Bengisu Sanisoğlu, Feray Kaya, Gülçin Otar Yener, Ferhat Demir, Ayşe Tanatar, Semanur Özdel and 5 more

Abstract readMulticenter Study
In one paragraph

Article in European journal of pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
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  8. 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

15 authors.

Zeynep ÖzaslanDepartment of Pediatric Rheumatology, Faculty of Medicine, MD, Kocaeli University, Kocaeli, Turkey. zeynepgozaluludag@gmail.com.ORCID http://orcid.org/0000-0003-2641-4140
Abdulvahap ŞenDepartment of Pediatric Rheumatology, Ankara Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0009-0000-8676-7197
Sıla Atamyıldız UçarDepartment of Pediatric Rheumatology, Health Sciences University, Umraniye Training and Research Hospital, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-4283-0921
Mustafa ÇakanDepartment of Pediatric Rheumatology, Zeynep Kamil Training and Research Hospital, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-1034-6406
Bengisu SanisoğluDepartment of Pediatrics, Department of Pediatric Rheumatology, İstanbul University, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-2774-9591
Feray KayaDepartment of Pediatric Rheumatology, İstanbul Medeniyet University, İstanbul, Turkey.ORCID http://orcid.org/0009-0000-9947-8298
Gülçin Otar YenerDepartment of Pediatric Rheumatology, Eskişehir City Hospital, Eskişehir, Turkey.ORCID http://orcid.org/0000-0003-2575-6309
Ferhat DemirDepartment of Pediatric Rheumatology, Acıbadem Ataşehir Hospital, Istanbul, Turkey.ORCID http://orcid.org/0000-0001-9801-925X
Ayşe TanatarDepartment of Pediatric Rheumatology, Gaziantep City Hospital, Gaziantep, Turkey.ORCID http://orcid.org/0000-0002-1386-4575
Semanur ÖzdelDepartment of Pediatric Rheumatology, Ankara Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0001-5602-4595
Kübra ÖztürkDepartment of Pediatric Rheumatology, İstanbul Medeniyet University, İstanbul, Turkey.ORCID http://orcid.org/0000-0003-0466-0228
Nihal ŞahinDepartment of Pediatric Rheumatology, Faculty of Medicine, MD, Kocaeli University, Kocaeli, Turkey.ORCID http://orcid.org/0000-0002-2122-6952
Hafize Emine SönmezDepartment of Pediatric Rheumatology, Faculty of Medicine, MD, Kocaeli University, Kocaeli, Turkey.ORCID http://orcid.org/0000-0002-9186-3068
Nuray Aktay AyazDepartment of Pediatrics, Department of Pediatric Rheumatology, İstanbul University, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-3594-7387
Betül SözeriDepartment of Pediatric Rheumatology, Health Sciences University, Umraniye Training and Research Hospital, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-5079-5644

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis syndrome (PFAPA) are the most common autoinflammatory syndromes in children. This study aimed to evaluate the clinical and laboratory parameters that may predict colchicine responsiveness.This retrospective, multicenter, cross-sectional study involved nine pediatric rheumatology centers from our country., The patients diagnosed with PFAPA were compared on the basis of their responses to colchicine. In the 806 (42.3% female 57.7% male) patients, the most common clinical findings were fever (100%), exudative tonsillitis (86.5%), pharyngitis (80.9%), and aphthous stomatitis (50.5%). The mean attack frequency was 13.5 ± 6.8 attacks per year lasting for a mean of 3.9 ± 1.1 days. Colchicine treatment was attempted in 519 (64.4%) patients, with 419 (80.7%) showing a favorable response. In patients who underwent MEFV gene analysis (70.8%), the most common variant was M694V heterozygous (16.8%). The presence of pharyngitis (p = 0.03, 95% CI 0.885 to 0.994), the presence of arthralgia (p = 0.04, 95% CI 0.169 to 0.958), and having more frequent attacks (p = 0.001, 95% CI 0.028 to 0.748) were found to be associated with colchicine unresponsiveness, whereas the carriage of the M694V variant (p = 0.001, 95% CI 0.065 to 0.242) was associated with colchicine responsiveness.

conclusionThis study identified the presence of pharyngitis, arthralgia, and increased attack frequency in patients with PFAPA as factors predicting colchicine unresponsiveness, whereas the carriage of the M694V variant emerged as a predictor of colchicine responsiveness. Predicting colchicine response at disease onset may facilitate a more effective management of PFAPA. WHAT IS KNOWN: • Colchicine treatment can be used in the prophylaxis of PFAPA disease. • Having the MEFV variant is the most commonly known factor in predicting response to colchicine. WHAT IS NEW: • The presence of pharyngitis or arthralgia, and more frequent attacks in PFAPA disease were found to be independently associated with colchicine unresponsiveness. • Carrying the M694V variant was identified as the sole factor predicting colchicine responsiveness.

Indexed as

ColchicineHereditary Autoinflammatory DiseasesLymphadenitisPharyngitisStomatitis, AphthousAdolescentChildChild, PreschoolCross-Sectional StudiesFemaleFeverHumansInfantMalePyrinRetrospective StudiesColchicineMEFV protein, humanPyrinColchicineMEFVPFAPATreatment response

Identifiers

PMID39085658
PMCPMC11413087

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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.