Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ 07110, USA.
Department of Pediatrics, Hackensack University Medical Center, Hackensack, NJ 07601, USA.
Viruses. 2023 Aug 5;15(8):1699. doi: 10.3390/v15081699.
New Jersey was among the first states impacted by the COVID-19 pandemic, with one of the highest overall death rates in the nation. Nevertheless, relatively few reports have been published focusing specifically on New Jersey. Here we report on molecular, clinical, and epidemiologic observations, from the largest healthcare network in the state, in a cohort of vaccinated and unvaccinated individuals with laboratory-confirmed SARS-CoV-2 infection. We conducted molecular surveillance of SARS-CoV-2-positive nasopharyngeal swabs collected in nine hospitals from December 2020 through June 2022, using both whole genome sequencing (WGS) and a real-time RT-PCR screening assay targeting spike protein mutations found in variants of concern (VOCs) within our region. De-identified clinical data were obtained retrospectively, including demographics, COVID-19 vaccination status, ICU admission, ventilator support, mortality, and medical history. Statistical analyses were performed to identify associations between SARS-CoV-2 variants, vaccination status, clinical outcomes, and medical risk factors. A total of 5007 SARS-CoV-2-positive nasopharyngeal swabs were successfully screened and/or sequenced. Variant screening identified three predominant VOCs, including Alpha ( = 714), Delta ( = 1877), and Omicron ( = 1802). Omicron isolates were further sub-typed as BA.1 ( = 899), BA.2 ( = 853), or BA.4/BA.5 ( = 50); the remaining 614 isolates were classified as "Other". Approximately 31.5% (1577/5007) of the samples were associated with vaccine breakthrough infections, which increased in frequency following the emergence of Delta and Omicron. Severe clinical outcomes included ICU admission (336/5007 = 6.7%), ventilator support (236/5007 = 4.7%), and mortality (430/5007 = 8.6%), with increasing age being the most significant contributor to each ( < 0.001). Unvaccinated individuals accounted for 79.7% (268/336) of ICU admissions, 78.3% (185/236) of ventilator cases, and 74.4% (320/430) of deaths. Highly significant ( < 0.001) increases in mortality were observed in individuals with cardiovascular disease, hypertension, cancer, diabetes, and hyperlipidemia, but not with obesity, thyroid disease, or respiratory disease. Significant differences ( < 0.001) in clinical outcomes were also noted between SARS-CoV-2 variants, including Delta, Omicron BA.1, and Omicron BA.2. Vaccination was associated with significantly improved clinical outcomes in our study, despite an increase in breakthrough infections associated with waning immunity, greater antigenic variability, or both. Underlying comorbidities contributed significantly to mortality in both vaccinated and unvaccinated individuals, with increasing risk based on the total number of comorbidities. Real-time RT-PCR-based screening facilitated timely identification of predominant variants using a minimal number of spike protein mutations, with faster turnaround time and reduced cost compared to WGS. Continued evolution of SARS-CoV-2 variants will likely require ongoing surveillance for new VOCs, with real-time assessment of clinical impact.
新泽西州是受 COVID-19 大流行影响的首批州之一,其总体死亡率在全美处于较高水平。然而,专门针对新泽西州的报告相对较少。在这里,我们报告了来自该州最大的医疗保健网络的分子、临床和流行病学观察结果,涉及接种疫苗和未接种疫苗的实验室确诊 SARS-CoV-2 感染个体。我们使用全基因组测序 (WGS) 和针对我们所在地区关注变体 (VOC) 中发现的刺突蛋白突变的实时 RT-PCR 筛选检测,对 2020 年 12 月至 2022 年 6 月期间从 9 家医院收集的 SARS-CoV-2 阳性鼻咽拭子进行了分子监测。我们回顾性地获得了去识别的临床数据,包括人口统计学、COVID-19 疫苗接种状态、重症监护病房 (ICU) 入院、呼吸机支持、死亡率和病史。进行了统计分析,以确定 SARS-CoV-2 变体、疫苗接种状态、临床结果和医疗风险因素之间的关联。共成功筛选和/或测序了 5007 份 SARS-CoV-2 阳性鼻咽拭子。变体筛查确定了三种主要的 VOC,包括 Alpha( = 714)、Delta( = 1877)和 Omicron( = 1802)。Omicron 分离株进一步分为 BA.1( = 899)、BA.2( = 853)或 BA.4/BA.5( = 50);其余 614 株被归类为“其他”。大约 31.5%(1577/5007)的样本与疫苗突破性感染有关,Delta 和 Omicron 出现后,这种感染的频率增加。严重的临床结果包括 ICU 入院(336/5007 = 6.7%)、呼吸机支持(236/5007 = 4.7%)和死亡率(430/5007 = 8.6%),年龄增长是导致每种情况的最重要因素(<0.001)。未接种疫苗的个体占 ICU 入院(268/336)、呼吸机病例(185/236)和死亡(320/430)的 79.7%、78.3%和 74.4%。在患有心血管疾病、高血压、癌症、糖尿病和高脂血症的个体中,观察到死亡率显著增加(<0.001),但在肥胖、甲状腺疾病或呼吸系统疾病患者中没有观察到这种情况。在 SARS-CoV-2 变体之间也观察到显著的临床结果差异,包括 Delta、Omicron BA.1 和 Omicron BA.2。尽管与免疫减弱、抗原变异性增加或两者相关的突破性感染增加,但疫苗接种与改善临床结果显著相关。在接种疫苗和未接种疫苗的个体中,基础合并症对死亡率的影响都很大,随着合并症总数的增加,风险也随之增加。基于实时 RT-PCR 的筛查通过使用最少数量的刺突蛋白突变来快速识别主要变体,与 WGS 相比,具有更快的周转时间和更低的成本。SARS-CoV-2 变体的持续演变可能需要持续监测新的 VOC,并实时评估临床影响。