Rhinology and Skull Base Research Group, Baton Rouge General Medical Center, 8585 Picardy Ave., Suite 210, Baton Rouge, LA 70809, USA.
Department of Otorhinolaryngology, Cairo University, Cairo 11451, Egypt.
Viruses. 2021 Mar 18;13(3):503. doi: 10.3390/v13030503.
COVID-19 has become a global pandemic of the highest priority. Multiple treatment protocols have been proposed worldwide with no definitive answer for acure. A prior retrospective study showed association between bitter taste receptor 38 (T2R38) phenotypes and the severity of COVID-19. Based on this, we proposed assessing the different T2R38 phenotypes response towards a targeted treatment protocol. Starting July 2020 till December 2020, we tested subjects for T2R38 phenotypic expression (supertasters, tasters, and nontasters). Subjects who were subsequently infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (diagnosed via PCR) were included. Based on their taster status, supertasters were given dexamethasone for 4 days; tasters were given azithromycin and dexamethasone +/- hydroxychloroquine for 7 days; and nontasters were given azithromycin and dexamethasone for 12 days. Subjects were followed prospectively and their outcomes were documented. Seven hundred forty-seven COVID-19 patients were included, with 184 (24.7%) supertasters, 371 (49.6%) tasters, and192 (25.7%) nontasters. The average duration of symptoms with the treatment protocol was 5 days for supertasters, 8.1 days for tasters, and 16.2 days for nontasters. Only three subjects (0.4%) required hospitalization (3/3 nontasters). Targeted treatment protocol showed significant correlation ( < 0.05) based on patients' T2R38 phenotypic expression. Assessing treatment protocols for COVID-19 patients according to their T2R38 phenotype could provide insight into the inconsistent results obtained from the different studies worldwide. Further study is warranted on the categorization of patients based on their T2R38 phenotype.
COVID-19 已成为全球高度优先关注的大流行病。全球提出了多种治疗方案,但尚无明确的治愈方法。先前的回顾性研究表明,苦味受体 38(T2R38)表型与 COVID-19 的严重程度之间存在关联。基于此,我们提出评估不同 T2R38 表型对靶向治疗方案的反应。从 2020 年 7 月到 2020 年 12 月,我们测试了受试者的 T2R38 表型表达(超敏者、敏者和非敏者)。随后通过 PCR 诊断出感染严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的受试者被纳入研究。根据他们的味觉状态,超敏者接受地塞米松治疗 4 天;敏者接受阿奇霉素和地塞米松 +/-羟氯喹治疗 7 天;非敏者接受阿奇霉素和地塞米松治疗 12 天。对受试者进行前瞻性随访并记录其结果。共纳入 747 例 COVID-19 患者,其中 184 例(24.7%)为超敏者,371 例(49.6%)为敏者,192 例(25.7%)为非敏者。接受治疗方案后,超敏者的症状平均持续 5 天,敏者为 8.1 天,非敏者为 16.2 天。只有 3 名受试者(0.4%)需要住院治疗(3/3 例非敏者)。基于患者的 T2R38 表型表达,靶向治疗方案显示出显著相关性(<0.05)。根据 T2R38 表型评估 COVID-19 患者的治疗方案可以为全球不同研究中获得的不一致结果提供深入了解。需要进一步研究根据患者的 T2R38 表型对患者进行分类。