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Table 1 Characteristics of the two long COVID cohorts derived from the GOLD study dataset

From: Genetic risk factors for severe and fatigue dominant long COVID and commonalities with ME/CFS identified by combinatorial analysis

 

Severe long COVID n = 1323

Fatigue dominant long COVID n = 1386

Cases (n = 459)

Controls (n = 864)

Cases (n = 477)

Controls (n = 909)

Age [median (IQR)]

45 (37–54)

54 (41–64)

45 (37–54)

54 (41–63)

Sex [n (%)] *

M: 129 (28.1)

M: 402 (46.5)

M: 121 (25.4)

M: 429 (47.2)

F: 329 (71.7)

F: 462 (53.5)

F: 355 (74.4)

F: 480 (52.8)

Self-reported ethnicity [n (%)] *

 Wh = White

Wh: 419 (91.3)

Wh: 781 (90.4)

Wh: 436 (91.4)

Wh: 825 (90.1)

 As = Asian

Mx: 19 (4.1)

As: 33 (3.8)

Mx: 17 (3.6)

As: 33 (3.6)

 Mx = Mixed

As: 12 (2.6)

Mx: 22 (2.5)

As: 14 (2.9)

Mx: 23 (2.5)

 Bl = Black

Ot: 4 (0.9)

Bl: 12 (1.4)

Bl: 4 (0.8)

Ot: 13 (1.4)

 Ot = Other

Bl: 2 (0.4)

Ot: 12 (1.4)

Ot: 3 (0.6)

Bl: 11 (1.2)

 No = None

No: 2 (0.4)

No: 1 (0.1)

No: 2 (0.4)

No: 1 (0.1)

Recovery time in days (Median [IQR])

479 (247–572)

18 (8–122)

484 (256–573)

18 (8–111)

COVID-19 related hospitalization [n (%)]

60 (13.1)

26 (3.0)

66 (13.8)

26 (2.9)

Reported problems after COVID-19 related hospital discharge [n (%)]

60 (13.1)

20 (2.3)

66 (13.8)

19 (2.1)

Hospitalized [n (%)]

46 (10.0)

7 (0.8)

50 (10.5)

8 (0.9)

Co-morbidities (pre-existing or post-COVID-19) [n (%)]

 Asthma†

108 (23.5)

121 (14.0)

110 (23.1)

133 (14.6)

 Alzheimer’s disease

0 (0.0)

1 (0.1)

0 (0.0)

1 (0.1)

 Coronary artery disease

2 (0.4)

13 (1.5)

3 (0.6)

13 (1.4)

 Chronic fatigue syndrome†

36 (7.8)

6 (0.7)

40 (8.4)

5 (0.6)

 Diabetes type 1

1 (0.2)

9 (1.0)

1 (0.2)

10 (1.1)

 Diabetes type 2

15 (3.3)

33 (3.8)

13 (2.7)

33 (3.6)

 Heart attack

5 (1.1)

7 (0.8)

3 (0.6)

7 (0.8)

 Irritable bowel syndrome†

65 (14.2)

41 (4.7)

74 (15.5)

47 (5.2)

 Kidney disease†

3 (0.7)

2 (0.2)

3 (0.6)

2 (0.2)

 Liver disease†

9 (2.0)

6 (0.7)

8 (1.7)

7 (0.8)

  1. Data for fields marked with asterisk (*) were not available for all individuals. Comorbidities marked with † were consistently over-represented in cases compared to controls in all cohorts