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Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations

Lara D. Veeken · 2006 · Vol. 45(6) · pp. 746–750
Helen J. LachmannBülent ŞengülTuğba YavuzşenDavid R. BoothS E BoothA BybeeJ. Ruth GallimoreMüjde SoytürkServet AkarMehmet TuncaPhilip N. Hawkins

Abstract

Substantial sub-clinical inflammation occurs widely and over prolonged periods in patients with FMF, indicating that the relatively infrequent clinically overt attacks represent the 'tip of the iceberg' in this disorder. Both basal and peak acute phase protein concentrations were greater in MEFV heterozygotes than in wild-type controls, regardless of mutation demonstrating a 'pro-inflammatory' phenotype among FMF carriers. Upregulation of the acute phase response among carriers of FMF may augment their innate host response and contribute to better resistance to infection.

Inflammasome and immune disordersIL-33, ST2, and ILC PathwaysMEFVFamilial Mediterranean feverMedicineAsymptomaticInternal medicineHeterozygote advantageGastroenterologyCompound heterozygosityPopulationImmunology

MeSH terms

PyrinAcute-Phase ReactionSerum Amyloid A ProteinC-Reactive ProteinCytoskeletal ProteinsGenotypeHeterozygoteHumansMutationFamilial Mediterranean FeverProspective StudiesBiomarkers

Funding

  • Wellcome Trust
  • Medical Research Council
Citations
370
FWCI
7.74
field-weighted impact
References
46
Percentile
98%
vs. same field & year
Citations per year
Cited by
Familial Mediterranean Fever
Medicine · 2012 · 1,039 citations
References
Familial Mediterranean fever
The American Journal of Medicine · 1967 · 1,122 citations
Familial Mediterranean Fever
Medicine · 2012 · 1,039 citations
Criteria for the diagnosis of familial mediterranean fever
Arthritis & Rheumatism · 1997 · 1,551 citations
Familial Mediterranean Fever (FMF) in Turkey
Medicine · 2005 · 757 citations
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