Prevalence of Chemosensory Dysfunction in COVID-19 Patients: A Systematic Review and Meta-analysis Reveals Significant Ethnic Differences

ACS Chem Neurosci. 2020 Oct 7;11(19):2944-2961. doi: 10.1021/acschemneuro.0c00460. Epub 2020 Sep 17.

Abstract

A significant proportion of people who test positive for COVID-19 have chemosensory deficits. However, the reported prevalence of these deficits in smell and taste varies widely, and the reason for the differences between studies is unclear. We determined the pooled prevalence of such chemosensory deficits in a systematic review and meta-analysis. We searched the COVID-19 portfolio of the National Institutes of Health for studies that reported the prevalence of smell or taste deficits or both in patients diagnosed with COVID-19. One-hundred-four studies reporting on 38 198 patients qualified and were subjected to a systematic review and meta-analysis. Estimated random prevalence of olfactory dysfunction was 43.0%, that of taste dysfunction was 44.6%, and that of overall chemosensory dysfunction was 47.4%. We examined the effects of age, gender, disease severity, and ethnicity on chemosensory dysfunction. Prevalence of smell or taste dysfunction or both decreased with older age, male gender, and disease severity. Ethnicity was highly significant: Caucasians had a three times higher prevalence of chemosensory dysfunctions (54.8%) than Asians (17.7%). The finding of geographic differences points to two causes that are not mutually exclusive. A virus mutation (D614G) may cause differing infectivity, while at the host level genetic, ethnicity-specific variants of the virus-binding entry proteins may facilitate virus entry in the olfactory epithelium and taste buds. Both explanations have major implications for infectivity, diagnosis, and management of the COVID-19 pandemic.

Keywords: SARS-CoV-2; anosmia; ethnicity; prevalence; smell; taste.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Age Factors
  • Angiotensin-Converting Enzyme 2
  • Asian People / statistics & numerical data*
  • Betacoronavirus / genetics
  • Betacoronavirus / pathogenicity
  • COVID-19
  • Coronavirus Infections / epidemiology
  • Coronavirus Infections / physiopathology*
  • Ethnicity
  • Genetic Variation
  • Humans
  • Olfaction Disorders / epidemiology
  • Olfaction Disorders / ethnology*
  • Olfaction Disorders / physiopathology
  • Pandemics
  • Peptidyl-Dipeptidase A / genetics
  • Pneumonia, Viral / epidemiology
  • Pneumonia, Viral / physiopathology*
  • Prevalence
  • SARS-CoV-2
  • Serine Endopeptidases / genetics
  • Severity of Illness Index
  • Sex Factors
  • White People / statistics & numerical data*

Substances

  • Peptidyl-Dipeptidase A
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • Serine Endopeptidases
  • TMPRSS2 protein, human