Prevalence of Antibodies to COVID-19 Due to Infection or Vaccination in US Adults.

Q3 Medicine
Robert L Stout, Steven J Rigatti
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引用次数: 0

Abstract

Objective: -Determine the seroprevalence of SARS-CoV-2 infection and vaccination in a population applying for life insurance.

Setting: -This is a cross-sectional study of 2584 US life insurance applicants, to determine the seroprevalence of antibodies to COVID-19. This convenience sample was selected on two consecutive days April 25-26, 2022.

Results: -For COVID-19, 97.3% are seropositive, and 63.9% have antibodies to nucleocapsid protein, a marker of prior infection. An additional, 33.7% have been vaccinated with no serologic evidence of infection.

Methodology: -Serum and urine samples from a nationwide group of insurance applicants for routine risk assessment were collected. The examination of applicants typically occurs, in their homes, their place of employment, or a clinic. The paramedic exam occurs 7-14 days after the insurance application. Before the exam, an office assistant calls the applicant and inquires if they have been in contact with a person with SARS-CoV-2, been ill within the last 2 weeks, felt sick, or recently had a fever. If the applicant answers yes, the exam is rescheduled. Before sample collection, the applicant reads and signs a consent form to release medical information and testing. Next, the examiner records the applicant's blood pressure, height, and weight. Then, a blood and a urine sample are collected and sent with the consent form to our laboratory via Federal Express. On April 25-26, 2022, we tested 2584 convenience samples from adult insurance applicants for the presence of antibodies to nucleocapsid and spike proteins from SARS-CoV-2. As a standard practice, we reported the client-specified test profile results to our life insurance carriers. In contrast, the COVID-19 test results were only available to the authors. Patient and Public Involvement.-There was no patient involvement in study design, reporting of results, or journal publication selection. There was patient consent to publish de-identified study results. No public involvement occurred in the creation or completion of the study. The authors thank the participants in this study for approving the use of their blood samples to further society's understanding of the SARS-CoV-19 pandemic. Ethics Review.-Western Institutional Review Board reviewed the study design and determined it to be exempt under the Common Rule and applicable guidance. Therefore, it is exempt under 45 CFR § 46.104(d)(4) from using de-identified study samples for epidemiologic investigation, WIRB Work Order #1-1324846-1. In addition, all test subjects had signed a consent allowing research of their blood and urine samples with the removal of personally identifiable information.

Results: -The combined seroprevalence for antibodies to nucleocapsid, a marker of prior infection, and antibodies to spike protein, an indicator of either previous infection or vaccination, was 97.3%. Higher infection rates occur in younger vs older age groups, with a non-statistical difference for vaccinated and acquired natural immunity. For the age group 16-84, the total estimated seroprevalence of COVID-19 in the US is 249 million cases.

Conclusions: -The US population has widespread immune resistance to current variants of COVID-19 due to prior infection or vaccination. The infectivity of new variants and silent disease, independent of previous infection or vaccination, are the driving force behind the sporadic increase in clinical SARS-CoV-2 cases.

美国成年人感染或接种新冠肺炎抗体的流行率。
目的:确定申请人寿保险人群中严重急性呼吸系统综合征冠状病毒2型感染和疫苗接种的血清流行率。背景:-这是一项针对2584名美国人寿保险申请人的横断面研究,旨在确定新冠肺炎抗体的血清流行率。该方便样本于2022年4月25日至26日连续两天选择。结果:-对于新冠肺炎,97.3%的人血清阳性,63.9%的人具有核衣壳蛋白抗体,核衣壳蛋白质是既往感染的标志物。另外,33.7%的人接种了疫苗,但没有感染的血清学证据。方法:从全国范围内的一组保险申请人中收集血清和尿液样本,用于常规风险评估。对申请人的检查通常在他们的家中、工作地点或诊所进行。护理人员检查在保险申请后7-14天进行。考试前,一名办公室助理打电话给申请人,询问他们是否与严重急性呼吸系统综合征冠状病毒2型患者有过接触,是否在过去两周内生病,是否感到不适,或最近发烧。如果申请人回答是,考试将重新安排。在采集样本之前,申请人阅读并签署同意书,以发布医疗信息和检测。接下来,审查员记录申请人的血压、身高和体重。然后,采集血液和尿液样本,并通过联邦快递将同意书发送到我们的实验室。2022年4月25日至26日,我们测试了来自成人保险申请人的2584份便利样本,以确定是否存在严重急性呼吸系统综合征冠状病毒2型核衣壳和刺突蛋白抗体。作为标准做法,我们向我们的人寿保险公司报告客户指定的测试档案结果。相比之下,新冠肺炎检测结果仅提供给作者。患者和公众参与-没有患者参与研究设计、结果报告或期刊出版物选择。患者同意公布未鉴定的研究结果。研究的创建或完成过程中未发生任何公众参与。作者感谢这项研究的参与者批准使用他们的血液样本,以进一步加深社会对严重急性呼吸系统综合征冠状病毒-19大流行的理解。道德审查-西方机构审查委员会审查了该研究设计,并根据共同规则和适用指南将其确定为豁免。因此,根据《美国联邦法规》第45卷第46.104(d)(4)条,它可以免于使用未鉴定的研究样本进行流行病学调查,WIRB工作指令#1-12324846-1。此外,所有受试者都签署了一份同意书,允许对他们的血液和尿液样本进行研究,并删除个人身份信息。结果:-既往感染的标志物核衣壳抗体和既往感染或疫苗接种的指标刺突蛋白抗体的联合血清流行率为97.3%。年轻组和老年组的感染率较高,接种疫苗和获得的自然免疫力存在非统计差异。对于16-84岁年龄组,美国新冠肺炎的总估计血清流行率为2.49亿例。结论:-由于先前感染或接种疫苗,美国人群对新冠肺炎的当前变种具有广泛的免疫抵抗力。新变种和无声疾病的传染性,独立于先前的感染或疫苗接种,是临床严重急性呼吸系统综合征冠状病毒2型病例零星增加的驱动力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
6
期刊介绍: The Journal of Insurance Medicine is a peer reviewed scientific journal sponsored by the American Academy of Insurance Medicine, and is published quarterly. Subscriptions to the Journal of Insurance Medicine are included in your AAIM membership.
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