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. 2016 Jun 23;5(1):94–103. doi: 10.1177/2050640616646525

Table 3.

The comparison of iron overload, liver fibrosis and liver function in HSS and N-HSS (median, range)

NTDT
TM
HSS (n = 83) N-HSS (n = 22) p value HSS (n = 65) N-HSS (n = 74) p value
SF 1283 (188–19,704) 601 (36–1590) p < 0.05 4538 (559–12,500) 4305 (121–14,724) p > 0.05
LIC 11.4 (0.8–43.0) 5.8 (0.6–20.7) p < 0.05 41.2 (8.4–43.0) 42.4 (21.1–43.0) p > 0.05
C IV 60 (9–25) 63 (18–138) p > 0.05 74 (52–126) 73 (56–157) p > 0.05
PIIINP 1.3 (0.0–53.4) 0.3 (0.0–8.7) p < 0.05 3.3 (0.0–41.6) 2.9 (0.0–94.7) p > 0.05
HA 25 (0–679) 11 (0–137) p < 0.05 64 (10–258) 67 (8–864) p > 0.05
ALT 19 (5–120) 15 (9–58) p > 0.05 42 (14–282) 37 (8–232) p > 0.05
AST 28 (11–119) 26 (12–74) p > 0.05 42 (18–177) 42 (17–175) p > 0.05

NTDT: non-transfusion-dependent thalassemia; TM: thalassemia major; SF: ferritin, ng/ml; LIC: liver iron overload, mg Fe/g dw; HA: hyaluronic acid, ng/ml; PIIINP: precollagen type III, ng/ml; C IV: collagen type IV, ng/ml; HSS: patients with history of hepatomegaly, splenomegaly or splenectomized; N-HSS: patients who without history of hepatomegaly, splenomegaly or splenectomized; ALT: alanine aminotransferase; AST: aspartate aminotransferase.