INTRODUCTION
Chronic urticaria (CU) has a lifelong prevalence of 0.5-1% in the United States.1 Reports have demonstrated that the disability suffered by CU patients is similar to that of patients with coronary artery disease.2 CU is defined as urticarial wheals and pruritus for duration of at least six weeks.3 Chronic urticaria
is associated with angioedema in 40 percent of cases.4 Approximately
50–80 percent chronic urticaria cases have no known etiology limiting the management approach to a focus on controlling
the symptoms.5-6 Though antihistamines are used as first-line treatment, as many as 50 percent of patients do not adequately respond to antihistamines alone.2 Second-line medications for patients unresponsive to antihistamines include dapsone, methotrexate,
cyclosporine, and mycophenolate mofetil, and other immunomodulatory
therapies.7-9 However, these medications can be associated with serious adverse effects, such as renal dysfunction,
liver function abnormalities, and pancytopenia.
Colchicine is an anti-inflammatory drug that is FDA approved for the treatment of gout, familial Mediterranean fever, Behcet´s disease,
and pericarditis.10 Case reports suggest a role for colchicine in the treatment of urticarial vasculitis.11-13 Colchicine induces mitotic arrest leading to inhibition of DNA synthesis and suppresses
leukocyte function.14 The mechanism of action involves suppressing cell-mediated immune responses via inhibition of immunoglobulin secretion, interleukin-1 production, histamine release, and HLA-DR expression.10,14 Colchicine has a known safety profile in children and adults. One study reported 6–13 years of colchicine use in children with familial Mediterranean fever, and colchicine treatment did not prompt early withdrawal for toxicity or effects on growth, development, and fertility of children.15-16 The common potential side effects of colchicine include
diarrhea (77% of patients who take high dose and 23% of patients who take low dose colchicine), nausea, and vomiting. Other less common adverse events include neutropenia, thrombocytopenia,
pancytopenia, myelosuppression, transaminitis, myoneuropathy, and renal dysfunction in individuals with a prior history of renal insufficiency.
This paper evaluates the therapeutic potential of colchicine, an alternative to immunosuppressive therapy for CU. We evaluated colchicine’s adverse effect profile and its effectiveness in achieving eradication of the symptoms of urticaria. In our study, we identified
patients through retrospective chart review of our institutional experience with colchicine for the treatment of recalcitrant CU.