Table 3.
Ref. Author (country) | COVID‐19 study population | Controls(if applicable) |
% group A patients (vs. control) P value (when applicable) |
% group O patients (vs. control) P value (when applicable) |
Blood group susceptibility to SARS‐CoV‐2 infection | Association with clinical outcomes and risk of death |
---|---|---|---|---|---|---|
Zhao J et al. [5] China |
1775 patients | 3694 normal individuals |
37·75 (32·16) P < 0·001 |
25·80 (33·84) P < 0·001 |
Yes, group A | Group A associated with higher risk of mortality than non group A |
Li J et al. [7] China |
2153 patients with COVID‐19 pneumonia | 3694 healthy controls |
38·0 (32·2) P < 0·001 |
25·7 (33·8) P < 0·001 |
Yes, group A |
Group A patients at higher risk of hospitalization following SARS‐CoV‐2 infection. Association with risk of mortality not assessed. |
Zeng X. et al. [51] China |
137 patients with mild pneumonia 97 patients with severe pneumonia |
Nil, Chinese population data used for comparison |
35·76 (28·39) 39·22 (28·39) |
32·45 (33·20) 26·47(33·20) |
Yes, group A |
Blood group A more susceptible to SARS‐CoV‐2. Blood groups not relevant to acute respiratory distress syndrome, acute kidney injury and mortality. |
Zietz M & Tatonetti [56] USA |
Observational data on 14,112 individuals tested for SARS‐CoV‐2 | None | 32·7 (32·7) | 46·9 (48·2) | Yes, group B and Rh(D) |
Risk of intubation decreased among group A and increased among groups AB and B. Risk of morality increased for group AB and decreased for groups A and B. Rh‐negative blood type protective for mortality. |
GÖKER H, et al . [49] Turkey |
186 patients | 1881 healthy controls |
57 (38) P < 0·001 |
24·8 (37·2) P = 0·001 |
Yes, group A | No significant effect of ABO and RhD on clinical outcomes including intubation, ICU stay and mortality |
Wu et al. [52] China |
187 patients | 1991 non‐COVID‐19 hospitalized patients |
36·9 (27·47) P = 0·006 |
21·92(30·19) P = 0·018 |
Yes, group A | Group A influenced clinical outcomes but no association with mortality |
Leaf RK et al. [48] USA |
561 critically ill patients. |
Nil, local population data used for comparison | 45·1 (39·8) | 37·8 (45·2) | Yes, group A | No association with any ABO phenotype and mortality |
Latz CA et al. [6] USA |
1289 patients | Nil | 34·2 (NA) | 45·5 (NA) | Yes, positive correlation with group B , AB & Rh(D)Negative with group O | No association with risk of intubation, peak of inflammatory markers and death |
Gerard C et al. [12] |
1175 patients | 3694 controls |
37·7 (32·2) P < 0·001 |
49·4 (57·6) |
Yes, presence of anti‐A antibodies in serum and more specifically IgG anti‐Aassociated with higher susceptibility to SARS‐CoV‐2 infection. |
Mortality risk not assessed |
Abdollahi A et al. [50] Iran |
397 patients | 500 normal controls |
40·3 (36) P = 0·19 |
28 (38) P = 0·002 |
Yes, group AB with higher susceptibility than other groups. |
No association of ABO or RHD phenotype with severity of disease. No association of ABO or RHD with mortality assessed. |
Hoiland et al. [4] Canada |
125 critically ill patients admitted to ICU | Nil, Comparison of blood group distributions between blood donor data was performed. |
37 (35) p‐0·60 No difference from blood donors |
Group O 43% (n = 41) No difference from blood donors |
Yes, group A and AB |
Higher proportion of COVID‐19 patients with blood group A or AB required mechanical ventilation, and continous renal replacement therapy and had longer ICU stay compared with patients with blood group O or B. |
Barnkob et al. [3] Denmark |
7422 COVID positive patients among 473 654 individuals tested |
466 232 COVID‐negative individuals |
More A (P <0·001), B (P = 0·011), and AB (P = 0·091) individuals were COVID positive. | 38·41% (95% CI, 37·30–39·50) group O compared with 41·70% (41·60–41·80) in controls | Yes, Decreased infection risk in group O |
ABO blood group as a risk factor for SARS‐CoV‐2 infection but not for hospitalization or death from COVID‐19. |