Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Department of Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
PLoS Med. 2023 Jul 24;20(7):e1004274. doi: 10.1371/journal.pmed.1004274. eCollection 2023 Jul.
The risk of incident diabetes following Coronavirus Disease 2019 (COVID-19) vaccination remains to be elucidated. Also, it is unclear whether the risk of incident diabetes after Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection is modified by vaccination status or differs by SARS-CoV-2 variants. We evaluated the incidence of diabetes following mRNA (BNT162b2), inactivated (CoronaVac) COVID-19 vaccines, and after SARS-CoV-2 infection.
In this population-based cohort study, individuals without known diabetes were identified from an electronic health database in Hong Kong. The first cohort included people who received ≥1 dose of COVID-19 vaccine and those who did not receive any COVID-19 vaccines up to September 2021. The second cohort consisted of confirmed COVID-19 patients and people who were never infected up to March 2022. Both cohorts were followed until August 15, 2022. A total of 325,715 COVID-19 vaccine recipients (CoronaVac: 167,337; BNT162b2: 158,378) and 145,199 COVID-19 patients were 1:1 matched to their respective controls using propensity score for various baseline characteristics. We also adjusted for previous SARS-CoV-2 infection when estimating the conditional probability of receiving vaccinations, and vaccination status when estimating the conditional probability of contracting SARS-CoV-2 infection. Hazard ratios (HRs) and 95% confidence intervals (CIs) for incident diabetes were estimated using Cox regression models. In the first cohort, we identified 5,760 and 4,411 diabetes cases after receiving CoronaVac and BNT162b2 vaccines, respectively. Upon a median follow-up of 384 to 386 days, there was no evidence of increased risks of incident diabetes following CoronaVac or BNT162b2 vaccination (CoronaVac: 9.08 versus 9.10 per 100,000 person-days, HR = 0.998 [95% CI 0.962 to 1.035]; BNT162b2: 7.41 versus 8.58, HR = 0.862 [0.828 to 0.897]), regardless of diabetes type. In the second cohort, we observed 2,109 cases of diabetes following SARS-CoV-2 infection. Upon a median follow-up of 164 days, SARS-CoV-2 infection was associated with significantly higher risk of incident diabetes (9.04 versus 7.38, HR = 1.225 [1.150 to 1.305])-mainly type 2 diabetes-regardless of predominant circulating variants, albeit lower with Omicron variants (p for interaction = 0.009). The number needed to harm at 6 months was 406 for 1 additional diabetes case. Subgroup analysis revealed no evidence of increased risk of incident diabetes among fully vaccinated COVID-19 survivors. Main limitations of our study included possible misclassification bias as type 1 diabetes was identified through diagnostic coding and possible residual confounders due to its observational nature.
There was no evidence of increased risks of incident diabetes following COVID-19 vaccination. The risk of incident diabetes increased following SARS-CoV-2 infection, mainly type 2 diabetes. The excess risk was lower, but still statistically significant, for Omicron variants. Fully vaccinated individuals might be protected from risks of incident diabetes following SARS-CoV-2 infection.
新冠肺炎(COVID-19)疫苗接种后发生糖尿病的风险仍需阐明。此外,SARS-CoV-2 感染后发生糖尿病的风险是否因疫苗接种状态而改变,以及是否因 SARS-CoV-2 变异体而不同,目前尚不清楚。我们评估了信使 RNA(BNT162b2)、灭活(CoronaVac)COVID-19 疫苗接种以及 SARS-CoV-2 感染后的糖尿病发病率。
在这项基于人群的队列研究中,我们从香港的电子健康数据库中确定了没有已知糖尿病的个体。第一队列包括至少接种了一剂 COVID-19 疫苗的人群和截至 2021 年 9 月未接种任何 COVID-19 疫苗的人群。第二队列由确诊的 COVID-19 患者和截至 2022 年 3 月从未感染过 COVID-19 的人群组成。两组均随访至 2022 年 8 月 15 日。共有 325715 名 COVID-19 疫苗接种者(CoronaVac:167337;BNT162b2:158378)和 145199 名 COVID-19 患者与各自的对照组通过各种基线特征的倾向评分进行了 1:1 匹配。在估计接种疫苗的条件概率时,我们还调整了以前的 SARS-CoV-2 感染情况,在估计感染 SARS-CoV-2 的条件概率时,我们调整了疫苗接种情况。使用 Cox 回归模型估计了糖尿病发病的风险比(HR)和 95%置信区间(CI)。在第一队列中,我们在接种 CoronaVac 和 BNT162b2 疫苗后分别发现了 5760 例和 4411 例糖尿病病例。在中位数为 384 至 386 天的随访期间,接种 CoronaVac 或 BNT162b2 疫苗后没有证据表明糖尿病发病风险增加(CoronaVac:每 10 万人日 9.08 例与 9.10 例,HR=0.998[95%CI 0.962 至 1.035];BNT162b2:7.41 例与 8.58 例,HR=0.862[0.828 至 0.897]),无论糖尿病类型如何。在第二队列中,我们观察到了 2109 例 SARS-CoV-2 感染后发生的糖尿病病例。在中位数为 164 天的随访期间,SARS-CoV-2 感染与糖尿病发病风险显著增加相关(9.04 例与 7.38 例,HR=1.225[1.150 至 1.305]),主要是 2 型糖尿病,尽管与 Omicron 变异体相比风险较低(p 交互作用=0.009)。每增加 1 例糖尿病的危害人数为 406 人。亚组分析表明,在完全接种 COVID-19 疫苗的幸存者中,没有证据表明发生糖尿病的风险增加。本研究的主要局限性包括可能存在 1 型糖尿病通过诊断编码确定的错误分类偏倚,以及由于其观察性性质可能存在残余混杂因素。
COVID-19 疫苗接种后没有证据表明糖尿病发病风险增加。SARS-CoV-2 感染后糖尿病发病风险增加,主要是 2 型糖尿病。对于 Omicron 变异体,风险虽低,但仍具有统计学意义。完全接种疫苗的个体可能免受 SARS-CoV-2 感染后发生糖尿病的风险。