Table 1.

Demographic and clinical characteristics of patients with VEXAS syndrome and thrombotic events

CharacteristicParticipants (N = 119)
Demographic characteristics  
Male sex, n (%) 119 (100) 
Age (y), median (range) 64.5 (39.0-86.0) 
Arterial thrombosis risk factors, n (%)  
Hypertension 59 (50) 
Obesity 38 (36) 
Smoking 29 (27) 
Hyperlipidemia 51 (44) 
Type II diabetes 29 (25) 
Atrial fibrillation 24 (21) 
Somatic UBA1 mutations, n (%) (n = 117) 
p.Met41Thr 69 (59) 
p.Met41Val 27 (23) 
p.Met41Leu 16 (14) 
Splice motif mutation 5 (4) 
VEXAS syndrome phenotype, n (%)  
Systemic symptoms (fever, fatigue, weight loss) 95 (80) 
Skin involvement (rash) 89 (75) 
Sweet syndrome 13 (11) 
Inflammatory eye disease (episcleritis, uveitis) 35 (30) 
Inner ear involvement (hearing loss, tinnitus, vertigo) 36 (30) 
Chondritis (ear, nose) 50 (42) 
Relapsing polychondritis 49 (41) 
Cardiac involvement (myocarditis, pericarditis, pericardial effusion) 7 (6) 
Pulmonary involvement (lung infiltrates, pleural effusion) 60 (50) 
Musculoskeletal involvement (arthritis, tenosynovitis) 76 (64) 
Macrocytic anemia 107 (90) 
MDS 36 (30) 
Plasma cell dyscrasia 21 (18) 
Thrombosis (VTE or arterial) 58 (49) 
Venous thrombotic events  
VTE, n (%) 49 (41) 
DVT, n (% of VTE) 41 (84) 
Proximal DVT, n (% of VTE) 27 (55) 
Distal DVT, n (% of VTE) 12 (24) 
PE, n (% of VTE) 17 (35) 
Unprovoked event, n (% of VTE) 30 (61) 
Recurrent event, n (% of VTE) 20 (41) 
Event while on anticoagulation, n (% of VTE) 10 (20) 
Arterial thrombotic events  
Any, n (%) 15 (13) 
Stroke, n (% of arterial) 5 (33) 
MI, n (% of arterial) 7 (47) 
Other, n (% of arterial) 3 (27) 
Recurrent event, n (% of arterial) 1 (7) 
CharacteristicParticipants (N = 119)
Demographic characteristics  
Male sex, n (%) 119 (100) 
Age (y), median (range) 64.5 (39.0-86.0) 
Arterial thrombosis risk factors, n (%)  
Hypertension 59 (50) 
Obesity 38 (36) 
Smoking 29 (27) 
Hyperlipidemia 51 (44) 
Type II diabetes 29 (25) 
Atrial fibrillation 24 (21) 
Somatic UBA1 mutations, n (%) (n = 117) 
p.Met41Thr 69 (59) 
p.Met41Val 27 (23) 
p.Met41Leu 16 (14) 
Splice motif mutation 5 (4) 
VEXAS syndrome phenotype, n (%)  
Systemic symptoms (fever, fatigue, weight loss) 95 (80) 
Skin involvement (rash) 89 (75) 
Sweet syndrome 13 (11) 
Inflammatory eye disease (episcleritis, uveitis) 35 (30) 
Inner ear involvement (hearing loss, tinnitus, vertigo) 36 (30) 
Chondritis (ear, nose) 50 (42) 
Relapsing polychondritis 49 (41) 
Cardiac involvement (myocarditis, pericarditis, pericardial effusion) 7 (6) 
Pulmonary involvement (lung infiltrates, pleural effusion) 60 (50) 
Musculoskeletal involvement (arthritis, tenosynovitis) 76 (64) 
Macrocytic anemia 107 (90) 
MDS 36 (30) 
Plasma cell dyscrasia 21 (18) 
Thrombosis (VTE or arterial) 58 (49) 
Venous thrombotic events  
VTE, n (%) 49 (41) 
DVT, n (% of VTE) 41 (84) 
Proximal DVT, n (% of VTE) 27 (55) 
Distal DVT, n (% of VTE) 12 (24) 
PE, n (% of VTE) 17 (35) 
Unprovoked event, n (% of VTE) 30 (61) 
Recurrent event, n (% of VTE) 20 (41) 
Event while on anticoagulation, n (% of VTE) 10 (20) 
Arterial thrombotic events  
Any, n (%) 15 (13) 
Stroke, n (% of arterial) 5 (33) 
MI, n (% of arterial) 7 (47) 
Other, n (% of arterial) 3 (27) 
Recurrent event, n (% of arterial) 1 (7) 

Obesity was defined as body mass index >30. Smoking history was defined as >10 pack-years. Missing data: n = 2 patients had missing UBA1 genotype data; n = 2 had missing hypertension, hyperlipidemia, diabetes, and atrial fibrillation data; n = 14 had missing body mass index; n = 10 had missing smoking data.

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