Key result
Elevated MMPs may drive coronary artery aneurysm development in Kawasaki disease.
Imbalances in matrix metalloproteinases and their inhibitors may play a key pathophysiological role in the development of coronary artery aneurysms in Kawasaki disease, highlighting a potential therapeutic target.
Kawasaki disease is an acute inflammatory syndrome that takes the form of systemic vasculitis, and predominantly affects children. Important complications of this disease are coronary artery dilation and aneurysm formation. Recent studies indicate that Kawasaki disease patients have elevated expression, activity, or protein levels of matrix metalloproteinases (MMPs), and suggest that imbalances in MMPs or MMP/tissue inhibitor of MMP (TIMP) play important pathophysiological roles in the development of coronary artery lesions in this disease. However, it remains unclear whether MMP activities at the site of coronary artery lesions are indeed increased. Further studies on the effects of MMP inhibition on coronary outcome are needed to define the roles of MMPs and TIMPs in the formation of coronary artery lesions in Kawasaki disease; findings of such studies may support the use of MMP inhibitors for the prevention of coronary artery complications in patients with this disease.
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Hideaki Senzaki (2006) conducted a review in Kawasaki disease. Matrix metalloproteinases (MMPs) was evaluated. Elevated expression and imbalances of matrix metalloproteinases (MMPs) may play a pathophysiological role in the development of coronary artery aneurysms in Kawasaki disease.
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