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既往罕见病对新冠病毒疾病严重程度、再感染及新冠长期症状的影响,以及疫苗接种和抗病毒治疗的调节作用:一项来自国家COVID-19合作数据库(N3C数据专区)的回顾性研究

Impact of Preexisting Rare Diseases on COVID-19 Severity, Reinfection, and Long COVID, and the Modifying Effects of Vaccination and Antiviral Therapy: A Retrospective Study from the N3C Data Enclave.

作者信息

Yadaw Arjun S, Sahner David K, Sid Eric, Chew Emily Y, Pichard Dominique, Mathé Ewy A

出版信息

medRxiv. 2025 Jul 10:2025.07.09.25331138. doi: 10.1101/2025.07.09.25331138.

DOI:10.1101/2025.07.09.25331138
PMID:40672484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12265750/
Abstract

BACKGROUND

Over 10,000 rare diseases (RDs) affect more than 300 million people globally, yet their influence on COVID-19 severity, reinfection risk, and long COVID remains poorly understood. This study evaluates the impact of RDs on these outcomes and examines the effectiveness of vaccination and antiviral treatments among individuals with and without RDs.

METHODS

We conducted a retrospective cohort study using harmonized electronic health records (EHRs) from the National COVID Cohort Collaborative (N3C), encompassing 21,704,702 individuals, including 4,825,605 with confirmed SARS-CoV-2 infection between Jan 1, 2020, and Jan 4, 2024. RDs were defined using 12,003 conditions curated from GARD and Orphanet, mapped to OMOP concepts, and classified into 18 RD classes based on medical specialty involvement. Primary outcomes included: (1) COVID-19 severity (hospitalization and life-threatening disease), (2) long COVID, and (3) SARS-CoV-2 reinfection. We applied multivariable logistic regression with inverse probability of treatment weighting and reported adjusted odds ratios with 95% confidence intervals and associated p-values. Models were controlled for demographics, comorbidities, and exposure to vaccination and antiviral treatments.

FINDINGS

Of 21,704,702 individuals, we identify 4,825,605 COVID-19 positive individuals, 6.36% had RDs, with markedly higher rates of rare disease (RD) patients that have life-threatening illness (16% vs. 6.1% without life-threatening illness) and that are hospitalized (13% vs. 6.0% without hospitalization). Otorhinolaryngologic diseases showed the highest risk of life-threatening outcomes (OR 4.51; 95% CI 3.81-5.33), followed by developmental defect during embryogenesis (OR 1.84; 95% CI 1.72-1.98) and cardiac conditions (OR 1.79; 95% CI 1.51-2.11). Hospitalization risk was highest for otorhinolaryngologic (OR 2.90; 95% CI 2.61-3.23), developmental defect during embryogenesis (OR 2.06; 95% CI 1.97-2.16), and hematologic and endocrine diseases (OR 1.81; 95% CI 1.75-1.87 and OR 1.81; 95% CI 1.64-1.99, respectively).In patients with RDs, vaccination alone or antiviral treatment alone was associated with reduced odds of life-threatening COVID-19 disease compared to non-vaccinated individuals (OR 0.71; 95% CI 0.66-0.77 and OR 0.33; 95% CI 0.26-0.42, respectively). The combination of both vaccination and antiviral treatment showed the greatest reduction in odds ratio (OR 0.24; 95% CI 0.20-0.27). Similar results were observed in patients without RDs. In contrast, vaccination or antiviral therapy alone, compared to no intervention, did not significantly reduce long COVID risk in RD patients, although these interventions alone did result in a lower odds ratio in patients without RD. However, their combination was protective in both groups. Vaccination alone, compared to no vaccination, also reduced the risk of reinfection across RD and non-RD populations.

INTERPRETATION

RD patients face elevated risks of severe COVID-19 outcomes. While vaccination and antivirals significantly reduce the acute severity of illness, their impact on long COVID appears limited in this population. Notably, vaccination was protective against COVID-19 reinfection in both RD and non-RD populations. These findings highlight the need for targeted strategies to protect RD patients beyond current interventions, particularly in preventing long-term complications.

FUNDING

This work was supported in part by the intramural and extramural programs at NCATS (ZIA ZICTR000410).

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/12265750/e8217ffd9d50/nihpp-2025.07.09.25331138v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/12265750/e40012c11b0c/nihpp-2025.07.09.25331138v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/12265750/53995bbfa3d2/nihpp-2025.07.09.25331138v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/12265750/e8217ffd9d50/nihpp-2025.07.09.25331138v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/12265750/e40012c11b0c/nihpp-2025.07.09.25331138v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/12265750/53995bbfa3d2/nihpp-2025.07.09.25331138v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd00/12265750/e8217ffd9d50/nihpp-2025.07.09.25331138v1-f0003.jpg
摘要

背景

全球有超过10000种罕见病影响着超过3亿人,但它们对新冠病毒疾病严重程度、再次感染风险和新冠长期症状的影响仍知之甚少。本研究评估了罕见病对这些结果的影响,并考察了有或没有罕见病的个体接种疫苗和抗病毒治疗的效果。

方法

我们使用来自国家新冠队列协作组(N3C)的统一电子健康记录(EHR)进行了一项回顾性队列研究,涵盖21704702名个体,其中包括2020年1月1日至2024年1月4日期间确诊感染新冠病毒的4825605人。罕见病根据从全球基因和罕见病信息资源(GARD)和Orphanet精心挑选的12003种病症来定义,映射到观察医疗结果合作组织(OMOP)概念,并根据医学专科涉及情况分为18个罕见病类别。主要结果包括:(1)新冠病毒疾病严重程度(住院和危及生命的疾病),(2)新冠长期症状,以及(3)新冠病毒再次感染。我们应用了具有治疗权重逆概率的多变量逻辑回归,并报告了调整后的优势比及95%置信区间和相关p值。模型对人口统计学、合并症以及接种疫苗和抗病毒治疗的暴露情况进行了控制。

结果

在21704702名个体中,我们识别出4825605名新冠病毒检测呈阳性的个体,其中6.36%患有罕见病,患有危及生命疾病的罕见病患者比例(16%对比无危及生命疾病的6.1%)和住院患者比例(13%对比未住院的6.0%)明显更高。耳鼻喉科疾病出现危及生命结果的风险最高(优势比4.51;95%置信区间3.81 - 5.33),其次是胚胎发育期间的发育缺陷(优势比1.84;95%置信区间1.72 - 1.98)和心脏疾病(优势比1.79;%置信区间1.51 - 2.11)。耳鼻喉科疾病的住院风险最高(优势比2.90;95%置信区间2.61 - 3.23),胚胎发育期间的发育缺陷(优势比2.06;95%置信区间1.97 - 2.16),以及血液学和内分泌疾病(分别为优势比1.81;95%置信区间1.75 - 1.87和优势比1.81;95%置信区间1.64 - 1.99)。在患有罕见病的患者中,与未接种疫苗的个体相比,单独接种疫苗或单独进行抗病毒治疗与降低危及生命的新冠病毒疾病几率相关(分别为优势比0.71;95%置信区间0.66 - 0.77和优势比0.33;95%置信区间0.26 - 0.42)。疫苗接种和抗病毒治疗相结合显示出最大的优势比降低(优势比0.24;95%置信区间0.20 - 0.27)。在没有罕见病的患者中也观察到了类似结果。相比之下,在患有罕见病的患者中,单独接种疫苗或抗病毒治疗与不进行干预相比,并没有显著降低新冠长期症状风险,尽管这些干预措施单独在没有罕见病的患者中确实导致了较低的优势比。然而,它们的联合在两组中都具有保护作用。与未接种疫苗相比,单独接种疫苗也降低了有罕见病和无罕见病人群的再次感染风险。

解读

患有罕见病的患者面临新冠病毒疾病严重后果的风险更高。虽然接种疫苗和抗病毒药物显著降低了疾病的急性严重程度,但它们对这一人群的新冠长期症状的影响似乎有限。值得注意的是,接种疫苗在有罕见病和无罕见病人群中对新冠病毒再次感染均具有保护作用。这些发现凸显了除当前干预措施外,还需要有针对性的策略来保护患有罕见病的患者,特别是在预防长期并发症方面。

资金支持

这项工作部分得到了美国国立转化医学科学研究所(NCATS)的内部和外部项目的支持(ZIA ZICTR000410)。

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