Matsumoto Akiko, Kodera Sachiko, Matsuura Tatsuya, Takayama Yoko, Yamada Yuya, Hirata Akimasa
Department of Social and Environmental Medicine, Saga University.
Center of Biomedical Physics and Information Technology, Nagoya Institute of Technology.
Environ Health Prev Med. 2024;29:52. doi: 10.1265/ehpm.24-00191.
An increased risk of diabetes after COVID-19 exposure has been reported in Caucasians during the early phase of the pandemic, but the effects across viral variants and in non-Caucasians have not been evaluated.
To address this gap, survival analyses were performed for five outbreak periods. From an anonymized health insurance database REZULT for the employees and their dependents of large companies or government agencies in Japan, 5 matched cohorts were generated based on age, sex, area of residence (47 prefectures), and 7 ranges of medical bills (COVID-19 exposed:unexposed = 1:4). Observation of each matching group began on the same day. Incident diabetes type 1 (T1D) and type 2 (T2D) were defined as the first claim during the target period, including at least 1 year before the start of observation.
T1D accounted for 0.8% of incident diabetes after the first COVID-19 exposure, similar to the non-exposed cohort. Most T2D in the COVID-19 cohort was observed within a few weeks. After further adjustment for the number of days from the start of observation to hospitalization (a time-dependent variable), the hazard ratio for incident T2D ranged from 14.1 to 20.0, with 95% confidence intervals (95%CI) of 8.7 to 32.0, during the 2-month follow-ups from the original strain outbreak to the Delta variant outbreak (by September 2021), and decreased to 2.0, with a 95%CI of 1.6 to 2.5, during the Omicron outbreak (by March 2022). No association was found during the BA.4/5 outbreak (until September 2022). Males had a higher risk, and the trend toward higher risk in older age groups was inconsistent across the periods.
Our large dataset, covering 2019-2023, reports for the first time the impact of COVID-19 on incident diabetes in non-Caucasians. The risk intensity and attributes of post-COVID-19 T2D were inconsistent across outbreak periods, suggesting diverse biological effects of different SARS-CoV-2 variants.
在疫情早期阶段,有报道称高加索人感染新冠病毒后患糖尿病的风险增加,但不同病毒变种对非高加索人的影响尚未得到评估。
为填补这一空白,对五个疫情暴发期进行了生存分析。从日本大型公司或政府机构员工及其家属的匿名健康保险数据库REZULT中,根据年龄、性别、居住地区(47个县)和7个医疗费用范围(新冠病毒暴露组:未暴露组 = 1:4)生成了5个匹配队列。每个匹配组的观察从同一天开始。1型糖尿病(T1D)和2型糖尿病(T2D)的发病定义为目标期间的首次理赔,包括观察开始前至少1年。
首次感染新冠病毒后,T1D占新发糖尿病的0.8%,与未暴露队列相似。新冠病毒队列中的大多数T2D在几周内被观察到。在进一步调整从观察开始到住院的天数(一个随时间变化的变量)后,从原始毒株暴发至德尔塔变种暴发(截至2021年9月)的2个月随访期间,新发T2D的风险比为14.1至20.0,95%置信区间(95%CI)为8.7至32.0,在奥密克戎毒株暴发期间(截至2022年3月)降至2.0,95%CI为1.6至2.5。在BA.4/5毒株暴发期间(截至2022年9月)未发现关联。男性风险更高,各时期老年组风险升高的趋势不一致。
我们涵盖2019 - 2023年的大型数据集首次报告了新冠病毒对非高加索人新发糖尿病的影响。新冠病毒感染后T2D的风险强度和特征在不同暴发期不一致,表明不同的严重急性呼吸综合征冠状病毒2变种具有不同的生物学效应。