Evidence map›Paper›PMID 31598594›Full record

ArticleArchives of rheumatology2019

Disease Severity and Genotype Affect Physical Growth in Children With Familial Mediterranean Fever.

Rabia Miray Kişla Ekinci, Sibel Balci, Eray Akay, Dilek Doğruel, Derya Ufuk Altintaş, Mustafa Yilmaz

Abstract read
In one paragraph

Article in Archives of rheumatology, 2019. 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
–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

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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.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rabia Miray Kişla EkinciDepartment of Pediatric Rheumatology, Çukurova University Faculty of Medicine, Adana, Turkey.
Sibel BalciDepartment of Pediatric Rheumatology, Çukurova University Faculty of Medicine, Adana, Turkey.
Eray AkayDepartment of Pediatrics, Çukurova University Faculty of Medicine, Adana, Turkey.
Dilek DoğruelDepartment of Pediatric Allergy and Immunology, Çukurova University Faculty of Medicine, Adana, Turkey.
Derya Ufuk AltintaşDepartment of Pediatric Allergy and Immunology, Çukurova University Faculty of Medicine, Adana, Turkey.
Mustafa YilmazDepartment of Pediatric Rheumatology, Çukurova University Faculty of Medicine, Adana, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study aims to analyze the growth parameters in children with familial Mediterranean fever (FMF) according to disease characteristics including genotype and disease severity by a recently validated tool in relatively more patients. Patients and methods: This retrospective study included 126 patients with FMF (70 males, 56 females; mean age 7.3±3.6 years; range, 4.1 to 18 years). MEditerranean FeVer (MEFV) gene analysis was performed with a molecular diagnostics tool by using a next-generation sequencing platform. Disease severity was determined for the first visit by the validated tool in children, international severity scoring system for FMF. Growth parameters including weight and height were investigated after standard deviation (SD) scores were calculated by anthropometric references in Turkish children. Results: Median follow-up duration was 74.7 months (range, 7.5 to 169 months). Ninety-three patients (73.8%) had at least one M694V mutation in MEFV gene. Six patients (4.8%) had severe disease, 58 (46%) had intermediate severity, and 62 (49.2%) had mild disease. Mean height SD score was significantly lower at last visit than before colchicine treatment. Initial and last height and weight SD scores were lower in patients with at least one M694V mutation than those without. However, the difference was statistically significant for only initial height SD score. We also found statistically significant lower initial height, final height, and weight SD scores in patients with intermediate severity-severe disease activity than mild disease. Conclusion: We advise physicians to score disease severity prospectively and pay attention to patients with intermediate severity-severe disease to avoid growth disturbances.

Indexed as

Disease severityfamilial Mediterranean fevergrowthinternational severity scoring system for familial Mediterranean feverM694V

Identifiers

PMID31598594
PMCPMC6768778

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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.