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Disease Severity and Genotype Affect Physical Growth in Children With Familial Mediterranean Fever
Rabia Miray Kişla Ekinci1, Sibel Balci1, Eray Akay2
1Department of Pediatric Rheumatology, Çukurova University Faculty of Medicine, Adana, Turkey.
Insights
Children with familial Mediterranean fever (FMF) and severe genotypes or intermediate-to-severe disease activity may experience growth disturbances. Monitoring disease severity is crucial for preventing impaired growth in pediatric FMF patients.
Area of Science:
- Pediatric Rheumatology
- Genetics
- Growth and Development
Background:
- Familial Mediterranean Fever (FMF) is a genetic autoinflammatory disorder.
- Growth parameters in children with FMF require careful evaluation.
- Disease genotype and severity are potential factors influencing growth.
Purpose of the Study:
- To analyze growth parameters in pediatric FMF patients.
- To correlate growth parameters with FMF genotype and disease severity.
- To identify risk factors for growth disturbances in FMF.
Main Methods:
- Retrospective study of 126 pediatric FMF patients.
- MEFV gene sequencing using next-generation sequencing.
- Disease severity assessed using a validated scoring system.
- Growth parameters (height, weight) analyzed using SD scores.
Main Results:
- Lower mean height SD scores observed at the last visit compared to pre-treatment.
- Patients with M694V mutations showed lower initial height SD scores.
- Intermediate to severe disease activity was associated with significantly lower initial and final height and weight SD scores compared to mild disease.
Conclusions:
- Physicians should prospectively assess FMF disease severity.
- Close attention to patients with intermediate-to-severe FMF is recommended to prevent growth issues.
- Early intervention and monitoring may mitigate growth disturbances in pediatric FMF.
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.
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