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Rheumatology 2014-Nov

Endothelial function in patients with familial Mediterranean fever-related amyloidosis and association with cardiovascular events.

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Entra registrati
Il collegamento viene salvato negli appunti
Mahmut I Yilmaz
Erkan Demirkaya
Cengizhan Acikel
Mehmet Saldir
Servet Akar
Tuncer Cayci
Mutlu Saglam
Hilmi U Unal
Mahmut Gok
Adem Polat

Parole chiave

Astratto

OBJECTIVE

Secondary amyloidosis is the most important complication of FMF and endothelial function is more severely impaired. Elevated asymmetric dimethyl arginine (ADMA) may mediate the excess cardiovascular disease (CVD) risk of this group. We aimed to compare endothelial function characteristics, including ADMA, in patients with FMF-related amyloidosis and primary glomerulopathies and to define risk factors for a CVD event.

METHODS

We undertook a cross-sectional study with prospective follow-up including consecutive patients with FMF-related amyloidosis (n = 98) or other non-diabetic glomerulopathies (n = 102). All patients had nephrotic-range proteinuria and normal glomerular filtration rate. Flow-mediated dilatation (FMD) was assessed and ADMA levels, CRP and pentraxin 3 (PTX3) were determined. Patients were followed for cardiovascular events.

RESULTS

Amyloidosis patients secondary to FMF showed higher levels of ADMA, CRP and PTX3 and lower FMD as compared with patients with other glomerulopathies. Cardiovascular events (n = 54) were registered during 3 years of follow-up. Increased ADMA levels and lower FMD were observed in patients with cardiovascular risk in both groups, but especially in individuals with amyloidosis.

CONCLUSIONS

Patients with FMF-related amyloidosis have increased CVD event risk, probably related to the high ADMA levels, elevated inflammatory markers and decreased FMD measures observed in these patients.

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