Effect of different doses of aspirin on the prognosis of Kawasaki disease

Kawasaki disease (KD) is a vascular inflammatory disease. KD is currently the most common acquired heart disease, and has already surpassed the rate of rheumatic heart disease [1]. The incidence of KD in Japan and South Korea is the highest in the world, with an incidence of 330 and 194.7 per 100,000 people, respectively. However, the incidence of KD in the United States, the United Kingdom, and Australia ranges from 8.39 to 25 per 100,000 people [2‐6]. KD primarily endangers children and can cause coronary artery aneurysms (CAAs). The incidence of CAA has fallen sharply after standardized treatment [7].

The initial treatment of KD with IVIG has generally reached consensus worldwide. However, there is still controversy about the appropriate aspirin dose to be used as a secondary cornerstone treatment. In North America, under the guidance of the America Heart Association (AHA) guidelines, high-dose aspirin (80–100 mg/kg/day) is used in the acute phase of KD [7]. In Asian regions under the guidance of the Japanese guidelines, moderate-dose aspirin (30–50 mg/kg/day) is widely used [8], and the aspirin dose in Western Europe is the same as that in Asia. Some Centers are opting to use low dose aspirin (3–5 mg/kg/day) [9].

Because of a lack of high-quality, randomized, and controlled trials, each dose has its supporting basis and cannot be completely unified. To balance the risks and benefits of aspirin, we performed a study to determine whether different doses of aspirin affect the outcome of KD including IVIG resistance and coronary artery damage.

Application of aspirin in KD was reported earlier than that of IVIG [12]. Previous studies [13] have suggested that high-dose aspirin combined with IVIG is beneficial for preventing coronary damage. Subsequent studies have indicated that coronary damage is only negatively correlated with the dose of IVIG, but not associated with aspirin [14]. However, to date, Japanese [15] and American [7] guidelines still recommend the use of moderate-dose aspirin (30–0 mg/kg/day) and high-dose aspirin (80–100 mg/kg/day), respectively. Clinically, because of the pharmaceutical dosage form, tablet aspirin is usually 50 mg, 100 mg, but the weight of the children varies. Clinical use of guidelines recommend 30–50 mg/kg of body weight, but the actual accurate calculation may be 20–50 mg. Coupled with the actual practice habits of different centers, some centers rapidly reduce the dose of aspirin to 3–5 mg/kg/day after being afebrile, and even some patients with atypical KD without fever before IVIG use usually have a low dose (3–5 mg/kg/day). Therefore, we took into account the case of a dose > 20 mg/kg/day in the acute phase of KD. In the present study, no significant difference was found in gender and IVIG treatment time among the groups. The difference found in age is related to the true clinical situation in the case of low-weight children and aspirin dosage forms. With a younger age and lower weight, the relative value of aspirin/weight is greater. At the same time, in younger children, clinicians are more careful and the rate of IVIG use is higher.

In recent years, many studies have been performed to determine the optimum dose of aspirin, and they have shown that the current recommended dose is not reasonable. Ogata et al. reported that there was no significant difference between moderate and high aspirin dose in KD [16]. A multicenter, randomized, single blind trial in Taiwan also showed that there was no significant difference in short-term coronary lesions of KD between high-dose and low-dose aspirin in the acute phase [17]. Huang et al. [18] reported that low-dose aspirin and moderate-dose aspirin had no effect on coronary artery damage in KD, although they did not show cardiac B-ultrasound time. Recent reports by Brooks et al. And Zheng et al. demonstrate that low-dose aspirin has there was no no significant difference in fever days and coronary artery damage rate between low-dose and traditional high-dose aspirin dose groups [19, 20]. This finding suggested that increasing the aspirin dose in the acute phase of KD may not needed. Furthermore, Migally et al. [21] found that the duration of high-dose aspirin had no relationship with long-term prognosis of the coronary artery. This evidence suggests that high-, moderate-, and low-dose aspirin appear to have no significant difference in the prognosis of KD. Pi et al. [22] reported that 11-dehydrothromboxane B2, the final product of the thromboxaneA2 pathway, was not reduced by using aspirin. Additionally, conflicting conclusions were reached by clinical researchers who showed that administration of different doses of aspirin was associated with protection against CAA. Dhanrajani et al. [23] found that IVIG resistance easily occurs with low-dose aspirin. Kim et al. [24] reported that moderate–high-dose aspirin was a risk factor for coronary artery CAA after adjusting for various factors compared with low-dose aspirin. In the present study, our findings showed that there was no significant differences in the incidence of CAA and the proportion of IVIG resistance between KD children who received different doses of aspirin. Our logistic analysis indicated that after adjusting for age, weight, sex, IVIG treatment options, IVIG treatment time, Hb levels, albumin levels, and FIB levels, the risk of CAA was not different among the three groups, indicating that there was no significant correlation between the dose of aspirin and the prevalence of CAA.

As a classic non-steroidal anti-inflammatory drug with acetylsalicylic acid, clinically, aspirin is widely used in preventing cardiovascular disease and postoperative thrombosis. Remarkably, aspirin combines anti-inflammatory (high dose) effects and anti-platelet (low dose) effects. Aspirin inhibits prostaglandin synthetase, reducing prostaglandin production to achieve anti-inflammatory and analgesic effects [25]. The anti-inflammatory effect of aspirin increases with dose accumulation. CRP levels proportionally reflect the grade of inflammation. In the present study, CRP levels were comparable among the groups. But the CRP levels of Group 3 (40–50 mg/kg/day) were lower than those of the other two groups. This finding indicates that relatively high doses of aspirin have better anti-inflammatory effects, although after treatment, CRP levels in the three groups all fell to within the normal range. Aspirin inhibits the Cyclooxygenase pathway and disrupts production of thromboxane thromboxaneA2, thereby reducing platelet aggregation and formation of a thrombus [26]. In the present study, significant differences were also found in PLT levels among three goups, the PLT count after treatment of 20–29 mg/kg/day of aspirin was the lowest among the groups, and to some extent, the relatively low dose of aspirin achieved an antiplatelet effect. Additionally, in the human body, aspirin is mainly absorbed in the stomach and small intestine, and rapidly hydrolyzed to salicylic acid. The rate of aspirin binding to plasma albumin is approximately 80–90%. However, during the acute phase of KD, the inflammatory responses of the gastrointestinal tract and a decrease in serum albumin levels lead to decreased efficacy of aspirin. After inflammation is relieved, gastrointestinal function and albumin levels are rapidly restored, which may even lead to drug toxicity [27]. Our results showed that Hb and albumin levels were significantly higher, and FIB levels were significantly lower in group 1 than those in the other two groups before treatment, while Hb and albumin levels in the three groups after treatment were the same as those before treatment. This finding suggested that the aspirin dose had little effect on these variables. While equally effective in therapeutic benefits, low-dose aspirin produces fewer side effects compared with traditional relatively high-dose aspirin.

Limitations of this study include its single-center and retrospective nature that is prone to indication bias, as well as a loss of follow-up data. However, our study reflects the real clinical condition. Additionally, the Z value could not be used to calibrate coronary damage results because of a lack of height data of children with KD. Therefore, a larger and more in-depth study is required and Z values should be used as possible variations. To the best of our knowledge, no prospective study has been performed to minimize moderate-dose aspirin for preventing CAA in KD.

In conclusion, our data show that in clinical practice, the commonly recommended dosage of 30–50 mg/kg/day of aspirin is not better than 20–29 mg/kg/day.