Table 1.

Clinical features of 18 patients tested for the pathogenic UBA1 variants

FeatureBeck et al2,* (N = 25)P1-8P9P10P11-18
Mutations, n/N p.Met41Thr (c.122T>C) (15/25) p.Met41Thr (c.122 T>C) (5/8) p.Met41Val (c.121A>G) (3/8) p.Ser56Phe (c.167C>T) p.(splice) (c.118-1G>C) UBA1 negative 
p.Met41Val (c.121A>G) (5/25) 
p.Met41Leu (c121A>C) (5/25) 
Demographics      
 Males, n/N (%) 25/25 (100) 8/8 Male Male 8/8 
 Age of onset, mean (range) 64 (45-80) 67 (60-74) 76 67 60 (40-71) 
 Deceased, n/N (%) 10/25 (40) 4/8 (50) No (current age 81 y) Yes (age of death 72 y) 1/8 
Laboratory findings      
 CRP, median (IQR), mg/L 73 (18-128) 100 (19-268) 48 (7-204) 48 (13-84) 98 (25-263) 
 Paraprotein, n/N  No (8/8) No IgGκ Yes 2/8 
IgAκ ×1 
IgAλ ×1 
Key Features      
 Fever, n (%) 23 (92) 8/8 (100) Yes Yes 8/8 
 Skin involvement, n (%) 22 (88) 7/8 (88) Painful nodular rash Painful nodular rash 5/8 
Painful nodular rash (4/8) Eczematous rash Painful nodular rash (2/8) 
Panniculitis (1/8) Erythema nodosum (1/1) 
Urticarial vasculitis (1/8) PG (1/1) 
Bullous vasculitis (1/8) Sweets (1/1) 
Eczematous rash (1/8) Nonspecific (1/1) 
Periorbital angioedema/cellulitis (1/8) Cellulitis like (1/1) 
 Pulmonary infiltrate, n (%) 18 (72) 2/8 (25) No No No 
 Ear/nose chondritis, n (%) 16 (64) 4/8 (50) No No 3/8 
 Venous thromboembolism, n (%) 11 (44) 1/8 (12.5) No No No 
 Macrocytic anemia, n (%) 24 (96) 8/8 (100) Yes Yes 4/4, 4/4 Normocytic anemia 
 Other, n/N N/A Weight loss (8/8) Myalgia, generalized stiffness, weight loss, fleeting arthralgia Orchitis, generalized arthritis Arthritis (2/8) 
Arthritis (1/8) Myalgia (3/8) 
Liver microabscesses (1/8) Myofasciitis (1/1) 
Interstitial nephritis (1/8)  
Ischemic colitis (1/8) Splenomegaly (1/1) 
 Principal diagnosis For details, see Beck et al AOSD (1/8) PMR/MDS Unclassified AOSD (1/8) 
Unclassified (6/8) MDS (3/8) 
RP (1/8) GCA/PMR (3/8) 
PG/sweets (1/) 
Bone marrow features      
 Cellularity, n/N ↑ (4/4) ↑ (2/2) ↑ ↑ ↑ (2/6) 
 Erythropoiesis, n/N ↓ (4/4) ↓ (2/2) ↑ with dysplastic change, nuclear inclusions ↓ with dysplastic change ↓ (2/6) 
 Granulopoiesis, n/N Expanded with dysplasia (4/4) Expanded with dysplasia (2/2) ↓ ↑ with minor dysplasia (<10%), vacuoles in promyelocytes Expanded with dysplasia (3/6) 
 Megakaryocytes, n/N ↑ with dysplastic change (4/4) ↑ with dysplastic change (1/2) ↑ with dysplastic change Normal number with dysplastic change ↑ with dysplastic change (3/6) 
Normal number with atypical forms (1/2) 
 
 Bone marrow vacuoles, n/N (2/4) (2/2) Undetermined Yes Undetermined (not commented) 
 Bone marrow diagnosis, n/N Nondiagnostic (3/4) Nondiagnostic (1/2) MDS with multilineage dysplasia MDS with multilineage dysplasia MDS (2/6) 
MDS (1/4) MDS with excess blasts MDS-AML (1/6) 
MGUS (2/6) 
Normal (1/6) 
Treatment history      
 Glucocorticoids, n,N (%) 25/25 (100) 8/8 (100) Yes PR Yes PR 8/8 
 Synthetic DMARDs, n/N For details, see Beck et al CyS (1/8) NR None None CyS (1/8) NR 
AZA (2/8) NR AZA (2/8) NR 
MTX (2/8) NR MTX (2/8) PR (1/1) 
CyC (2/8) NR MMF (2/8) NR 
MMF (2/8) NR Dapsone (1/8) NR 
Dapsone (1/8) NR Leflunomide (1/8) NR 
 Biological DMARDs, n/N For details, see Beck et al Tocilizumab (3/4) 2 NR, 1 PR None None Infliximab (1/1) R 
Anakinra (1/4) NR Anakinra (1/1) R 
Rituximab (1/4) NR Tocilizumab (1/1) R 
FeatureBeck et al2,* (N = 25)P1-8P9P10P11-18
Mutations, n/N p.Met41Thr (c.122T>C) (15/25) p.Met41Thr (c.122 T>C) (5/8) p.Met41Val (c.121A>G) (3/8) p.Ser56Phe (c.167C>T) p.(splice) (c.118-1G>C) UBA1 negative 
p.Met41Val (c.121A>G) (5/25) 
p.Met41Leu (c121A>C) (5/25) 
Demographics      
 Males, n/N (%) 25/25 (100) 8/8 Male Male 8/8 
 Age of onset, mean (range) 64 (45-80) 67 (60-74) 76 67 60 (40-71) 
 Deceased, n/N (%) 10/25 (40) 4/8 (50) No (current age 81 y) Yes (age of death 72 y) 1/8 
Laboratory findings      
 CRP, median (IQR), mg/L 73 (18-128) 100 (19-268) 48 (7-204) 48 (13-84) 98 (25-263) 
 Paraprotein, n/N  No (8/8) No IgGκ Yes 2/8 
IgAκ ×1 
IgAλ ×1 
Key Features      
 Fever, n (%) 23 (92) 8/8 (100) Yes Yes 8/8 
 Skin involvement, n (%) 22 (88) 7/8 (88) Painful nodular rash Painful nodular rash 5/8 
Painful nodular rash (4/8) Eczematous rash Painful nodular rash (2/8) 
Panniculitis (1/8) Erythema nodosum (1/1) 
Urticarial vasculitis (1/8) PG (1/1) 
Bullous vasculitis (1/8) Sweets (1/1) 
Eczematous rash (1/8) Nonspecific (1/1) 
Periorbital angioedema/cellulitis (1/8) Cellulitis like (1/1) 
 Pulmonary infiltrate, n (%) 18 (72) 2/8 (25) No No No 
 Ear/nose chondritis, n (%) 16 (64) 4/8 (50) No No 3/8 
 Venous thromboembolism, n (%) 11 (44) 1/8 (12.5) No No No 
 Macrocytic anemia, n (%) 24 (96) 8/8 (100) Yes Yes 4/4, 4/4 Normocytic anemia 
 Other, n/N N/A Weight loss (8/8) Myalgia, generalized stiffness, weight loss, fleeting arthralgia Orchitis, generalized arthritis Arthritis (2/8) 
Arthritis (1/8) Myalgia (3/8) 
Liver microabscesses (1/8) Myofasciitis (1/1) 
Interstitial nephritis (1/8)  
Ischemic colitis (1/8) Splenomegaly (1/1) 
 Principal diagnosis For details, see Beck et al AOSD (1/8) PMR/MDS Unclassified AOSD (1/8) 
Unclassified (6/8) MDS (3/8) 
RP (1/8) GCA/PMR (3/8) 
PG/sweets (1/) 
Bone marrow features      
 Cellularity, n/N ↑ (4/4) ↑ (2/2) ↑ ↑ ↑ (2/6) 
 Erythropoiesis, n/N ↓ (4/4) ↓ (2/2) ↑ with dysplastic change, nuclear inclusions ↓ with dysplastic change ↓ (2/6) 
 Granulopoiesis, n/N Expanded with dysplasia (4/4) Expanded with dysplasia (2/2) ↓ ↑ with minor dysplasia (<10%), vacuoles in promyelocytes Expanded with dysplasia (3/6) 
 Megakaryocytes, n/N ↑ with dysplastic change (4/4) ↑ with dysplastic change (1/2) ↑ with dysplastic change Normal number with dysplastic change ↑ with dysplastic change (3/6) 
Normal number with atypical forms (1/2) 
 
 Bone marrow vacuoles, n/N (2/4) (2/2) Undetermined Yes Undetermined (not commented) 
 Bone marrow diagnosis, n/N Nondiagnostic (3/4) Nondiagnostic (1/2) MDS with multilineage dysplasia MDS with multilineage dysplasia MDS (2/6) 
MDS (1/4) MDS with excess blasts MDS-AML (1/6) 
MGUS (2/6) 
Normal (1/6) 
Treatment history      
 Glucocorticoids, n,N (%) 25/25 (100) 8/8 (100) Yes PR Yes PR 8/8 
 Synthetic DMARDs, n/N For details, see Beck et al CyS (1/8) NR None None CyS (1/8) NR 
AZA (2/8) NR AZA (2/8) NR 
MTX (2/8) NR MTX (2/8) PR (1/1) 
CyC (2/8) NR MMF (2/8) NR 
MMF (2/8) NR Dapsone (1/8) NR 
Dapsone (1/8) NR Leflunomide (1/8) NR 
 Biological DMARDs, n/N For details, see Beck et al Tocilizumab (3/4) 2 NR, 1 PR None None Infliximab (1/1) R 
Anakinra (1/4) NR Anakinra (1/1) R 
Rituximab (1/4) NR Tocilizumab (1/1) R 

↑, above normal range; ↓, below normal range; AML, acute myeloid leukaemia; AOSD, adult onset stills disease; AZA, azathioprine; CRP, C reactive protein; CyS, cyclosporin; CyC, cyclophosphamide; DMARDs, disease-modifying antirheumatic drugs; GCA, giant cell arteritis; MDS, myelodysplastic syndrome; MGUS, monoclonal gammopathy of undetermined significance; MMF, mycophenolate; MTX, methotrexate; N/A, not applicable; NR, nonresponder; PG, pyoderma gangrenous; PMR, polymyalgia rheumatica; PR, partial response; R, response; RP, relapsing polychondritis.

*

Shown as median and interquartile range (IQR).

Summary of bone marrow features of 4 confirmed VEXAS cases which were included in Beck et al.

Good response to steroids, but now steroid dependent for control of inflammatory symptoms.

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