On-demand anakinra treatment is effective in mevalonate kinase deficiency

被引:119
作者
Bodar, E. J. [1 ]
Kuijk, L. M. [2 ]
Drenth, J. P. H. [3 ]
van der Meer, J. W. M. [1 ]
Simon, A. [1 ]
Frenkel, J. [2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Gen Internal Med, NL-6500 HB Nijmegen, Netherlands
[2] Univ Med Ctr Utrecht, Dept Gen Paediat, Utrecht, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Gastroenterol & Hepatol, NL-6500 HB Nijmegen, Netherlands
关键词
HYPERIMMUNOGLOBULINEMIA-D; INFLAMMATORY ATTACKS; FOLLOW-UP; THERAPY;
D O I
10.1136/ard.2011.149922
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Mevalonate kinase deficiency (MKD) is a hereditary autoinflammatory syndrome marked by recurrent attacks of fever and inflammation. Severe enzyme deficiency results in mevalonic aciduria (MA) and milder deficiency in hyperimmunoglobulin D syndrome (HIDS). Treatment remains a challenge. Objective To observe the effect of the recombinant interleukin-1 receptor antagonist anakinra in patients with MKD. Methods A prospective observational study was undertaken. Two patients with MA started continuous treatment with anakinra (1-2 mg/kg/day) and nine patients with HIDS chose between continuous treatment and on-demand treatment (starting at first symptoms of attack, 100 mg/day or 1 mg/kg/day for 5-7 days). Results Anakinra induced partial remission in one patient with MA but there was no response in the other patient with MA. In one patient with HIDS continuous treatment induced complete remission for 7 months but was stopped because of side effects. Eight patients with HIDS preferred on-demand treatment from the start. This induced a clinical response (>= 50% reduction in duration) in 8 of 12 treated attacks without a change in attack frequency. Anakinra prevented fever attacks due to vaccination without inhibiting antibody induction. No major side effects were seen. Conclusions On-demand treatment with anakinra in HIDS decreases the duration and severity of fever attacks. Because of the burden of daily injections and relatively long asymptomatic intervals of HIDS, all patients with HIDS preferred on-demand treatment.
引用
收藏
页码:2155 / 2158
页数:4
相关论文
共 17 条
  • [1] Bodar EJ, 2005, NETH J MED, V63, P260
  • [2] Anakinra is safe and effective in controlling hyperimmunoglobulinaemia D syndrome-associated febrile crisis
    Cailliez, M.
    Garaix, F.
    Rousset-Rouviere, C.
    Bruno, D.
    Kone-Paut, I.
    Sarles, J.
    Chabrol, B.
    Tsimaratos, M.
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (06) : 763 - 763
  • [3] Schnitzler syndrome: Beyond the case reports: Review and follow-up of 94 patients with an emphasis on prognosis and treatment
    de Koning, Heleen D.
    Bodar, Evelien J.
    van der Meer, Jos W. M.
    Simon, Anna
    [J]. SEMINARS IN ARTHRITIS AND RHEUMATISM, 2007, 37 (03) : 137 - 148
  • [4] Blocking interleukin-1β in acute and chronic autoinflammatory diseases
    Dinarello, C. A.
    [J]. JOURNAL OF INTERNAL MEDICINE, 2011, 269 (01) : 16 - 28
  • [5] Therapy of autoinflammatory syndromes
    Hoffman, Hal M.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2009, 124 (06) : 1129 - 1138
  • [6] Hyperimmunoglobulinemia D and periodic fever syndrome in children. Review on therapy with biological drugs and case report
    Korppi, M.
    van Gijn, M. E.
    Antila, K.
    [J]. ACTA PAEDIATRICA, 2011, 100 (01) : 21 - 25
  • [7] Efficacy and Safety of Anakinra Therapy in Pediatric and Adult Patients With the Autoinflammatory Muckle-Wells Syndrome
    Kuemmerle-Deschner, Jasmin B.
    Tyrrell, Pascal N.
    Koetter, Ina
    Wittkowski, Helmut
    Bialkowski, Anja
    Tzaribachev, Nicolai
    Lohse, Peter
    Koitchev, Assen
    Deuter, Christoph
    Foell, Dirk
    Benseler, Susanne M.
    [J]. ARTHRITIS AND RHEUMATISM, 2011, 63 (03): : 840 - 849
  • [8] HMG-CoA reductase inhibition induces IL-1β release through Rac1/PI3K/PKB-dependent caspase-1 activation
    Kuijk, Loes M.
    Beekman, Jeffrey M.
    Koster, Janet
    Waterham, Hans R.
    Frenkel, Joost
    Coffer, Paul J.
    [J]. BLOOD, 2008, 112 (09) : 3563 - 3573
  • [9] Mevalonate kinase deficiency syndrome with structural damage responsive to anakinra
    Lequerre, T.
    Vittecoq, O.
    Pouplin, S.
    Klemmer, N.
    Mejjad, O.
    Daragon, A.
    Prieur, A. M.
    Le Loet, X.
    [J]. RHEUMATOLOGY, 2007, 46 (12) : 1860 - 1862
  • [10] Phenotype, genotype, and sustained response to anakinra in 22 patients with autoinflammatory disease associated with CIAS-1/NALP3 mutations
    Leslie, Kieron S.
    Lachmann, Helen J.
    Bruning, Elizabeth
    McGrath, John A.
    Bybee, Alison
    Gallimore, J. Ruth
    Roberts, Philip F.
    Woo, Patricia
    Grattan, Clive E.
    Hawkins, Philip N.
    [J]. ARCHIVES OF DERMATOLOGY, 2006, 142 (12) : 1591 - 1597