ObvioHealth, 3452 Lake Lynda Dr., Bld. 100 Ste 151, Orlando, FL, 32832, USA.
Cardiovasc Diabetol. 2022 Feb 14;21(1):24. doi: 10.1186/s12933-022-01462-3.
Pre-existing cardiometabolic comorbidities place SARS-CoV-2 positive patients at a greater risk for poorer clinical course and mortality than those without it. We aimed to analyze real-world registry data focused primarily on participants with cardiometabolic diseases (CMD), which were remotely obtained via a digital platform.
Participants were divided into two groups: CMD or no cardiometabolic disease (non-CMD). They were evaluated based on their medical history, current medications/supplements, COVID-19 status, demographics, and baseline characteristics. The frequency of medications/supplements for CMD were compared using relative risks and 95% confidence intervals. The WHO (Five) Well-Being Index (WHO-5) were collected monthly for 6 months to assess psychological well-being which included cheerfulness, calmness, vigor, rest, and engagement with daily activities of interest.
The 791 enrollees represented 49 U.S. states. The CMD group had significantly higher (p < 0.0001) BMI (mean + 3.04 kg/m) and age (mean + 9.15 years) compared to non-CMD group. In the CMD group, participants who tested positive for COVID-19 had lower (p < 0.0001) well-being scores than those without COVID-19. For the 274 participants on CMD medications/supplements, there was no statistical difference in risk of COVID-19 contracture based on medication/supplement type; however, all six participants who were not being treated for CMD were COVID-19 positive (RR ~ 104). For 89 participants who were on treatment for diabetes or insulin resistance, there was a 90% reduced risk of COVID-19 incidence (p = 0.0187).
The well-being score of the CMD group was dependent on whether they tested positive for COVID-19. Type of CMD treatment did not impact COVID-19 status, but absence of treatment significantly increased COVID-19 incidence. With respect to SARS-CoV-2, our analysis supports continued use of the statins, ACE-I, ARBs, and diabetes medications in CMD patients.
ClinicalTrials.gov Identifier: NCT04348942.
与没有合并症的患者相比,合并心血管代谢合并症的 SARS-CoV-2 阳性患者临床预后和死亡率更差。我们旨在分析主要针对心血管代谢疾病(CMD)患者的真实世界登记数据,这些数据是通过数字平台远程获得的。
参与者分为两组:CMD 或无心血管代谢疾病(非 CMD)。根据他们的病史、当前药物/补充剂、COVID-19 状态、人口统计学和基线特征进行评估。使用相对风险和 95%置信区间比较 CMD 药物/补充剂的使用频率。每月收集 6 个月的世界卫生组织(五)幸福感指数(WHO-5),以评估心理健康,包括愉快、平静、活力、休息和参与感兴趣的日常活动。
791 名参与者代表美国 49 个州。CMD 组的 BMI(平均+3.04kg/m)和年龄(平均+9.15 岁)明显高于非 CMD 组(p<0.0001)。在 CMD 组中,COVID-19 检测呈阳性的参与者的幸福感评分明显低于未感染 COVID-19 的参与者(p<0.0001)。对于 274 名服用 CMD 药物/补充剂的参与者,根据药物/补充剂类型,COVID-19 感染的风险没有统计学差异;然而,所有 6 名未接受 CMD 治疗的参与者均 COVID-19 检测呈阳性(RR~104)。对于 89 名接受糖尿病或胰岛素抵抗治疗的参与者,COVID-19 发病风险降低了 90%(p=0.0187)。
CMD 组的幸福感评分取决于他们是否 COVID-19 检测呈阳性。CMD 治疗类型不影响 COVID-19 状态,但缺乏治疗显著增加 COVID-19 的发病率。关于 SARS-CoV-2,我们的分析支持在 CMD 患者中继续使用他汀类药物、ACE-I、ARB 和糖尿病药物。
ClinicalTrials.gov 标识符:NCT04348942。