Choroidal Thickness Changes in the Acute Attack Period in Patients with Familial Mediterranean Fever

Fatih C Gundogan1, Fahrettin Akay, Salih Uzun

  • 1Department of Ophthalmology, Gulhane Military Medical Academy, Ankara, Turkey.

Abstract

Insights

Familial Mediterranean fever (FMF) patients show increased choroidal thickness during acute attacks, linked to inflammation. This finding suggests potential ocular involvement in FMF inflammatory processes.

Area of Science:

  • Ophthalmology
  • Rheumatology
  • Internal Medicine

Background:

  • Familial Mediterranean fever (FMF) is a genetic autoinflammatory disorder characterized by recurrent episodes of fever and serositis.
  • Ocular manifestations in FMF are not well-defined, though inflammation is a key feature of the disease.

Purpose of the Study:

  • To investigate potential changes in choroidal thickness during acute attacks of familial Mediterranean fever (FMF).
  • To explore the relationship between choroidal thickness, inflammatory markers, and clinical findings in FMF patients.

Main Methods:

  • A comparative study involving 50 FMF patients during acute attacks and 50 healthy controls.
  • Choroidal thickness was measured using spectral-domain optical coherence tomography (SD-OCT) at multiple points around the foveola.
  • Blood inflammatory markers including white blood cell count, erythrocyte sedimentation rate (ESR), fibrinogen, and C-reactive protein (CRP) were assessed.

Main Results:

  • FMF patients exhibited significantly increased choroidal thickness compared to controls during acute attacks (p < 0.05).
  • Choroidal thickness positively correlated with ESR, fibrinogen, and particularly CRP levels.
  • No significant association was found between clinical FMF manifestations (peritonitis, arthritis, pleuritis) and choroidal thickness.

Conclusions:

  • Elevated choroidal thickness during acute FMF attacks may be attributed to inflammatory and edematous changes within the choroid.
  • These findings suggest that the choroid could be affected during the systemic inflammation associated with FMF.

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