Kawasaki disease (KD) is a common vasculitis disease in childhood and usually affects children under 5 years of age.<br><br>Pathogen infection is a potential trigger for susceptible children.<br><br>It is believed by Marrani and others that patients with KD have a strong congenital immune response, which causes inflammatory damage to systemic blood vessels. However, unlike most infectious diseases, there are significant differences in race, indicating that genetics has certain pathogenic mechanisms in the disease.<br><br>It has identified several susceptible genes (e.g. ITPKC, CASP3, CD40 and ORAI) and chromosome regions associated with KD through genome-wide association and genome-wide interlocking studies.<br><br>Genetic testing can make early diagnosis and treatment of KD easier and reduce inappropriate treatment in patients with other diagnoses. Coronary artery injury is the most important complication of Kawasaki disease, which can lead to severe coronary artery stenosis and ischemic heart disease.<br>For KD, clinically, the treatment plan of propylene globulin combined with aspirin is mainly. The use of intravenous immunoglobulin (IVIG) and aspirin greatly reduced the occurrence of coronary artery lesions in sick children, aspirin is a nonsteroidal anti-inflammatory drug, with anti-heat, pain relief effect, but also can inhibit the inflammatory reaction mediated by prostatin, inhibit angiotisitis response, but also has the role of plate plate aggregation, coronary damage has a certain control effect. In addition, aspirin is also able to regulate the hypothyclin thermothermia center, effectively control the body temperature of patients, for patients with Kawasaki disease has a high safety. The combined application of immunoglobulin and aspirin can play a synergy in alleviating symptoms and improving the inflammatory response of patients, but there is currently no uniform standard for the dose and dosage cycle of immunoglobulin, Dietz and others advocate that the dose of immunoglobulin is high dose, with a view to quickly controlling the disease and alleviating symptoms. Dionne and other studies have concluded that high-dose immunoglobulin intravenous injection (2 g / kg, single application) and conventional dose (1g/kg) immunoglobulin intravenous injection can not only play a more advantageous clinical therapeutic effect, but also safe and effective. At the same time, coronary artery lesions also have a very beneficial preventive effect, can reduce its occurrence rate to less than 5%.<br>The mechanism of vascular damage in patients with Kawasaki disease is thought to be related to the activation of monocyte/macrophage systems in the body, thereby releasing a large number of inflammatory media and inflammatory factors, causing endodertic damage to blood vessels. The research shows that TNF-a can stimulate T cells to produce various inflammatory factors and aggravate inflammatory reactions, which play an important role in the body's inflammatory response and immunomodulation. CRP can be significantly increased in the early stages of inflammatory reactions. IL-6 is an inflammatory factor that stimulates the proliferation and differentiation of T- and B-cells, increases the release of inflammatory factors and aggravates inflammatory reactions. This study also confirmed that the above-mentioned inflammatory factor levels increased significantly in the pre-treatment serum of patients with Kawasaki disease, suggesting the presence of a high inflammatory response state in the body. Therefore, for the treatment of Kawasaki disease, reducing the level of inflammatory factors and protecting the endothor function of blood vessels is also the key.<br>Although the role of corticosteroids is still controversial, more literature supports the possible benefits of glucoticoids in the treatment of the disease. Gamez and others believe that the first-line treatment for the disease includes intravenous use of immunoglobulin and corticosteroids, and that low-dose, short-course hormone therapy has lower side effects and is more likely to be accepted. Studies such as Miyata have also confirmed that small doses of pernisone acetate have relatively small side effects.<br>Our study confirmed that, on the basis of oral aspirin therapy, high-dose propylene globulin single-dose impact therapy combined with small-dose percetic acid pernicone therapy, patients with TNF-a, CRP, IL-6 and other inflammatory factors decreased the level of more significantly than conventional propylene globulin therapy (p).
正在翻译中..