COVID-19 疫苗接种反应与糖尿病患者发生突破性感染的风险:源自社区报告者的队列研究。

Q2 Medicine JMIR Diabetes Pub Date : 2024-02-27 DOI:10.2196/45536
Nancy A Dreyer, Kendall B Knuth, Yiqiong Xie, Matthew W Reynolds, Christina D Mack
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引用次数: 0

摘要

背景:这项探索性研究比较了自称患有糖尿病的人与未自称患有糖尿病的人自我报告的COVID-19疫苗副作用和突破性感染:本研究使用个人报告数据来评估患有糖尿病的成年人与未报告患有糖尿病的成年人对 COVID-19 疫苗副作用的感知差异:这是一项回顾性队列研究,使用的是居住在美国的 18 岁及以上成年人在线提供的数据。在 2021 年 3 月 19 日至 2022 年 7 月 16 日期间自愿自行加入 IQVIA COVID-19 积极研究体验项目的参与者报告了临床和人口统计学信息、COVID-19 疫苗接种情况、是否出现过任何副作用、检测确认的感染情况,并同意与处方索赔挂钩。本研究没有区分糖尿病前期或 1 型和 2 型糖尿病,也没有核实 COVID-19 检测呈阳性的报告。个人报告的药物使用情况通过药房报销单进行验证,链接数据的一个子集用于药物影响的敏感性分析。多变量逻辑回归用于估算糖尿病状态下疫苗副作用或突破性感染的调整几率比例,并对年龄、性别、教育程度、种族、民族(西班牙裔或拉丁裔)、体重指数、吸烟者、接种过流感疫苗、疫苗生产商和所有医疗条件进行调整。对糖尿病药物特异性疫苗副作用的评估以图表的形式展示,以支持对用于控制糖尿病的各种药物和药物组合的副作用差异程度的研究:结果:糖尿病患者(n=724)在接种COVID-19疫苗后两周内出现的副作用少于非糖尿病患者(n=6417;平均2.7,SD 2.0 vs 平均3.1,SD 2.0)。糖尿病患者出现特定副作用或任何副作用的调整后风险较低,在最长随访时间内,疲劳和头痛的风险显著降低,但突破性感染的风险没有差异。无论是使用自我报告的药物使用情况,还是仅使用由同时报告患有糖尿病的人的药房健康保险索赔确认的糖尿病药物,糖尿病药物使用情况都不会持续影响特定副作用的风险:结论:与未报告患有糖尿病的参与者相比,糖尿病患者报告的疫苗副作用较少,发生突破性感染的风险相似:试验注册:ClinicalTrials.gov NCT04368065;https://clinicaltrials.gov/study/NCT04368065。
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COVID-19 Vaccination Reactions and Risk of Breakthrough Infections Among People With Diabetes: Cohort Study Derived From Community Reporters.

Background: This exploratory study compares self-reported COVID-19 vaccine side effects and breakthrough infections in people who described themselves as having diabetes with those who did not identify as having diabetes.

Objective: The study uses person-reported data to evaluate differences in the perception of COVID-19 vaccine side effects between adults with diabetes and those who did not report having diabetes.

Methods: This is a retrospective cohort study conducted using data provided online by adults aged 18 years and older residing in the United States. The participants who voluntarily self-enrolled between March 19, 2021, and July 16, 2022, in the IQVIA COVID-19 Active Research Experience project reported clinical and demographic information, COVID-19 vaccination, whether they had experienced any side effects, test-confirmed infections, and consented to linkage with prescription claims. No distinction was made for this study to differentiate prediabetes or type 1 and type 2 diabetes nor to verify reports of positive COVID-19 tests. Person-reported medication use was validated using pharmacy claims and a subset of the linked data was used for a sensitivity analysis of medication effects. Multivariate logistic regression was used to estimate the adjusted odds ratios of vaccine side effects or breakthrough infections by diabetic status, adjusting for age, gender, education, race, ethnicity (Hispanic or Latino), BMI, smoker, receipt of an influenza vaccine, vaccine manufacturer, and all medical conditions. Evaluations of diabetes medication-specific vaccine side effects are illustrated graphically to support the examination of the magnitude of side effect differences for various medications and combinations of medications used to manage diabetes.

Results: People with diabetes (n=724) reported experiencing fewer side effects within 2 weeks of vaccination for COVID-19 than those without diabetes (n=6417; mean 2.7, SD 2.0 vs mean 3.1, SD 2.0). The adjusted risk of having a specific side effect or any side effect was lower among those with diabetes, with significant reductions in fatigue and headache but no differences in breakthrough infections over participants' maximum follow-up time. Diabetes medication use did not consistently affect the risk of specific side effects, either using self-reported medication use or using only diabetes medications that were confirmed by pharmacy health insurance claims for people who also reported having diabetes.

Conclusions: People with diabetes reported fewer vaccine side effects than participants not reporting having diabetes, with a similar risk of breakthrough infection.

Trial registration: ClinicalTrials.gov NCT04368065; https://clinicaltrials.gov/study/NCT04368065.

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来源期刊
JMIR Diabetes
JMIR Diabetes Computer Science-Computer Science Applications
CiteScore
4.00
自引率
0.00%
发文量
35
审稿时长
16 weeks
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