Table 2.

Association of TEs and clinical characteristics at diagnosis

VariableTE
(n = 56)
No TE
(n = 211)
P value
Demographics    
Age at diagnosis, median (IQR), y 42 (26.3-58) 46 (27-62) .5353 
Sex, n (%)   .0964 
Male 30 (53.6) 86 (40.8)  
Female 26 (46.4) 125 (59.2)  
Laboratory markers, median (IQR)    
Hb (g/dL) 9.5 (8.1-11.2) 9.2 (8.1-10.7) .8396 
ANC (×109/L) 2.4 (1.2-3.9) 1.4 (0.8-2.5) .0212 
Platelets (×109/L) 85 (28-137.5) 37 (18-93) .0064 
Absolute reticulocyte count (×103/μL) 106 (61-184) 77.5 (33.8-142) .0392 
D-dimer (mg/L) 1335 (337.5-3023) 360 (237-820) .0004 
LDH (U/L) 603 (362-939) 318 (311-902) .0070 
AST (U/L) 37 (18.5-61.5) 25 (18-42.3) .1701 
ALT (U/L) 24 (17.5-56) 20.5 (14-31.8) .0606 
Creatinine (mg/dL) 0.8 (0.66-1.07) 0.8 (0.69-1.0) .7700 
Albumin (g/dL) 4 (3.8-4.5) 4.3 (4.1-4.7) .0030 
C-reactive protein (mg/dL) 7.65 (2.15-19.45) 0.7 (0.2-3) .0459 
Presence of CHIP, n (%)  8 of 35 (23%) 27 of 151 (19%) .4798 
Disease characteristics    
Prior AA, n (%) 31 (55.4) 161 (76.3) .5505 
AA to PNH, time in mo, median (IQR) 23.4 (1.5-126.4) 36.9 (3.7-85.2) .1385 
PIGA mutant, n (%) 23 (67.7) 124 (61.4) .5684 
PIGA VAF, % (IQR) 35.4 (14.6-47.4) 11.6 (5.8-36.2) .0172  
Granulocyte clone size, median (IQR) 71.3 (42.7-92.2) 12.8 (0.6-70.2) <.0001 
RBC clone size, median (IQR) 17.3 (5.9-49.3) 1.8 (0.2-19.6) <.0001 
Type II–dominant RBC clone, n (%) 13 (39.4) 13 (15.1) .0064  
Type III–dominant RBC clone, n (%) 20 (60.6) 73 (84.9)  
VariableTE
(n = 56)
No TE
(n = 211)
P value
Demographics    
Age at diagnosis, median (IQR), y 42 (26.3-58) 46 (27-62) .5353 
Sex, n (%)   .0964 
Male 30 (53.6) 86 (40.8)  
Female 26 (46.4) 125 (59.2)  
Laboratory markers, median (IQR)    
Hb (g/dL) 9.5 (8.1-11.2) 9.2 (8.1-10.7) .8396 
ANC (×109/L) 2.4 (1.2-3.9) 1.4 (0.8-2.5) .0212 
Platelets (×109/L) 85 (28-137.5) 37 (18-93) .0064 
Absolute reticulocyte count (×103/μL) 106 (61-184) 77.5 (33.8-142) .0392 
D-dimer (mg/L) 1335 (337.5-3023) 360 (237-820) .0004 
LDH (U/L) 603 (362-939) 318 (311-902) .0070 
AST (U/L) 37 (18.5-61.5) 25 (18-42.3) .1701 
ALT (U/L) 24 (17.5-56) 20.5 (14-31.8) .0606 
Creatinine (mg/dL) 0.8 (0.66-1.07) 0.8 (0.69-1.0) .7700 
Albumin (g/dL) 4 (3.8-4.5) 4.3 (4.1-4.7) .0030 
C-reactive protein (mg/dL) 7.65 (2.15-19.45) 0.7 (0.2-3) .0459 
Presence of CHIP, n (%)  8 of 35 (23%) 27 of 151 (19%) .4798 
Disease characteristics    
Prior AA, n (%) 31 (55.4) 161 (76.3) .5505 
AA to PNH, time in mo, median (IQR) 23.4 (1.5-126.4) 36.9 (3.7-85.2) .1385 
PIGA mutant, n (%) 23 (67.7) 124 (61.4) .5684 
PIGA VAF, % (IQR) 35.4 (14.6-47.4) 11.6 (5.8-36.2) .0172  
Granulocyte clone size, median (IQR) 71.3 (42.7-92.2) 12.8 (0.6-70.2) <.0001 
RBC clone size, median (IQR) 17.3 (5.9-49.3) 1.8 (0.2-19.6) <.0001 
Type II–dominant RBC clone, n (%) 13 (39.4) 13 (15.1) .0064  
Type III–dominant RBC clone, n (%) 20 (60.6) 73 (84.9)  

ALT, alanine aminotransferase; CHIP, clonal hematopoiesis of indeterminate potential; Hb, hemoglobin.

Bold values indicate statistical significance.

Missing data (PIGA molecular information available in 91 patients, and PNH RBC clone type available in 100 patients; myeloid NGS available for 186 patients).

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