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. 2012 Aug 10;51(3):178–184. doi: 10.3164/jcbn.12-11

Table 2.

Comparison of the clinical background factors of the patients, separated according to their baseline serum albumin concentrations

Parameter Albumin below 4.0 g/dl
Albumin 4.0 g/dl or more
Treatment group Control group p value* Treatment group Control group p value*
Number 4 11 26 21
 Gender (male) 1 (25.0%) 6 (54.5%) 0.5692 14 (51.8%) 13 (48.1%) 0.8307
Age 68.1 ± 1.2 63.2 ± 10.9 0.4016 54.5 ± 13.2 58.0 ± 9.1 0.2974
BMI 23.4 ± 0.2 22.5 ± 1.5 0.4454 23.2 ± 3.5 23.1 ± 3.0 0.9625
AST (U/L) 73.0 ± 17.0 66.1 ± 30.2 0.7664 62.6 ± 26.1 54.7 ± 20.0 0.2771
ALT (U/L) 96.6 ± 65.5 56.8 ± 27.3 0.1119 88.7 ± 38.4 65.3 ± 38.0 0.0524
Platelet count (×104/µL) 10.5 ± 3.0 15.2 ± 5.7 0.1400 15.9 ± 4.1 15.8 ± 5.3 0.9081
Zinc concentration (µg/dl) 55.0 ± 11.4 51.7 ± 10.5 0.6097 60.6 ± 8.7 56.0 ± 9.6 0.0879
Albumin (g/dl) 3.7 ± 0.3 3.8 ± 0.1 0.3627 4.2 ± 0.2 4.2 ± 0.2 0.8351
Observation period (year) 7.4 ± 3.8 5.8 ± 2.4 0.3437 8.7 ± 2.0 7.7 ± 3.2 0.2266

*p<0.005. Mann-Whitney U test, chi-square test. Treatment group: patients with polaprezinc administration. Control group: patients without polaprezinc administration. The study subjects were grouped into those with baseline serum albumin concentrations below 4.0 g/dl in and those with serum albumin concentrations of 4.0 g/dl or more. Comparison of the clinical characteristics of patients with and without polaprezinc administration.