PW02-002 - Single MVK mutation and recurrent fevers

Results 31 pts with mutations in MVK were evaluated: 22 had 2 mutations (21 with V377I and 1 other mutation; 1 with V203A/H380R), 9 had only 1 mutation after testing the whole gene (8 with V377I, 1 with I268V). The carrier frequency of V377I in our control Caucasian population is 0.3% (2/739). In contrast, in 344 independent cases of recurrent fever submitted for MVK testing, 8 bore a single copy of V377I for a frequency of 2.3%. Clinical or laboratory presentation at the time of a flare was compared between the 2 groups. There was no significant difference with regard to age of onset, duration of flares, frequency of flares, flares after immunizations, GI symptoms, oral ulcers, sore throat, arthralgia, or adenopathy associated with flares. Rash was more common in pts with 2 mutations, 20/22 compared to 4/9 in those with one mutation (p=.01). While there was no difference in level of IgG, IgA was increased in those with 2 mutations (452 +230 mg/dl) compared to those with 1 mutation (230 + 175) (p=.01), as well as level of IgD, (95 + 95, 2 mutations, vs. 8.3 + 7.4, 1 mutation, p=.01) Since there was no significant difference in clinical presentation, other than presence of rash and levels of IgA and IgD, pts were considered together to evaluate their therapeutic responses. Of 8 pts treated with colchicine, 7 reported no response, 1 reported some improvement. Of 27 pts treated with prednisone at the time of a flare, 18 noted some improvement; 7 reported either none or shortening of the interval before next flare. Of 15 pts receiving montelukast, 4 reported some improvement; 11 reported none. Of 19 pts receiving intermittent anakinra at the time of a flare, 13 reported some improvement, 3 too early to assess efficacy, and 3 no improvement including one who developed acute renal failure. 5 pts received daily anakinra, with 4 reporting some improvement and 1 too early to assess. Of 9 pts receiving etanercept, 4 reported improvement, 5 report none.