Mukhija Sasha, Sunog Max, Magdamo Colin, Albers Mark W
Neurology Department, Massachusetts General Hospital, Boston, USA (Mukhija, Sunog, Magdamo, Albers).
Laboratory of Systems Pharmacology, Harvard Medical School, Boston, USA (Mukhija, Magdamo, Albers).
medRxiv. 2025 Mar 28:2025.03.26.25324688. doi: 10.1101/2025.03.26.25324688.
Severe COVID-19 infection has been associated with neurological complications, but its role in accelerating cognitive decline remains unclear.
To determine whether individuals hospitalized for severe COVID-19 exhibit a higher incidence of new onset cognitive impairment compared to those hospitalized for other conditions.
A retrospective study emulating a target trial using Mass General Brigham electronic health records (March 2020-August 2024). The causal effect of COVID-19 hospitalization was estimated via cumulative incidence functions accounting for the competing risk of death.
Multicenter hospital-based study across the Mass General Brigham healthcare system.
A total of 221613 hospitalized patients met the eligibility criteria, including 6454 (2.0%) admitted due to COVID-19 and 215159 (98.0%) for all other conditions. Patients were excluded if they had less than three months of follow-up (due to censoring, cognitive impairment, or death), were younger than 55 years at baseline, or had no prior visit to Mass General Brigham in the year before baseline.
The primary outcome was new-onset cognitive impairment, identified via ICD codes and dementia medication prescriptions. The primary analysis estimated the hazard ratio for cognitive impairment with COVID-19 hospitalization relative to other hospitalizations, along with the risk difference at 4.5 years estimated via cumulative incidence functions. Inverse propensity score weighting was used to balance covariates (age, sex, comorbidities, hospitalization period).
Among eligible patients (mean [SD] age, 69.55 [9.42] years, 55% female), those hospitalized for COVID-19 were significantly older and had more comorbidities (p < 0.05). COVID-19 hospitalization was associated with a higher risk of developing cognitive impairment (Hazard Ratio: 1.14 [95% CI: 1.02-1.30], P = 0.018). At 4.5 years, the cumulative incidence of cognitive impairment was 12.5% [95% CI: 11.3-13.5] in the COVID-19 group, compared to 11.6% [95% CI: 11.1-12.1] in the non-COVID-19 group.
Severe COVID-19 infection was associated with an elevated risk of developing clinically recognized cognitive impairment. Future studies are needed to validate findings in other health care settings. Early screening and intervention for cognitive decline may help optimize long-term outcomes for COVID-19 patients.
重症新型冠状病毒肺炎(COVID-19)感染与神经并发症相关,但其在加速认知衰退方面的作用仍不明确。
确定因重症COVID-19住院的个体与因其他疾病住院的个体相比,新发认知障碍的发生率是否更高。
一项使用麻省总医院布莱根分院电子健康记录进行的回顾性研究(2020年3月至2024年8月),模拟目标试验。通过考虑死亡竞争风险的累积发病率函数来估计COVID-19住院的因果效应。
基于麻省总医院布莱根医疗系统的多中心医院研究。
共有221613名住院患者符合纳入标准,其中6454名(2.0%)因COVID-19入院,215159名(98.0%)因所有其他疾病入院。如果患者的随访时间少于三个月(由于审查、认知障碍或死亡)、基线时年龄小于55岁或在基线前一年未去过麻省总医院布莱根分院,则被排除。
主要结局是新发认知障碍,通过国际疾病分类代码和痴呆症药物处方确定。主要分析估计了COVID-19住院患者与其他住院患者相比发生认知障碍的风险比,以及通过累积发病率函数估计的4.5年时的风险差异。使用逆倾向评分加权来平衡协变量(年龄、性别、合并症、住院时间)。
在符合条件的患者中(平均[标准差]年龄为69.55[9.42]岁,55%为女性),因COVID-19住院的患者年龄显著更大,合并症更多(p<0.05)。COVID-19住院与发生认知障碍的较高风险相关(风险比:1.14[95%置信区间:1.02-1.30],P = 0.018)。在4.5年时,COVID-19组认知障碍的累积发病率为12.5%[95%置信区间:11.3-13.5],而非COVID-19组为11.6%[95%置信区间:11.1-12.1]。
重症COVID-19感染与发生临床认可的认知障碍的风险升高相关。未来需要在其他医疗环境中验证研究结果。对认知衰退进行早期筛查和干预可能有助于优化COVID-19患者的长期结局。