Aims: Vitamin D serves an important role in regulating immune response mechanisms, and
vitamin D deficiency has been associated with unfavourable outcomes in patients infected
with chronic hepatitis C. Patients with advanced liver disease frequently suffer from
vitamin D deficiency. However, it remains unknown whether vitamin D deficiency has
an influence on mortality in these patients. Thus, we prospectively studied a cohort
of patients with advanced liver disease to assess the influence of vitamin D deficiency
on survival.
Patients and methods: Ninety-two patients with liver cirrhosis (mean age, 55 years; range, 19–76 years;
66% males; CTP stage C, 41%) were included in our prospective single-center survival
study. Serum for determination of vitamin D status was available from 61 patients.
AUC analysis, Chi-square statistics and multivariate binary regression analysis were
used to determine the optimal cut-off. Vitamin D levels were determined using a chemiluminescence
immunoassay.
Results: Median vitamin D levels were 8.2ng/ml (range <4ng/ml –95.8ng/ml) Overall, 51% of
patients (31/61) died during a minimal follow-up of 24 months. AUC analysis determined
a vitamin D level of 6ng/ml as optimal cut-off for discriminating survivors from non-survivors.
Kaplan-Meier analysis of survival confirmed low vitamin D levels as a significant
predictor of death (p=0.004).
Of note, multivariate analysis identified low vitamin D levels (OR=6.3; CI: 1.2–31.2;
p=0.024) and MELD scores (OR=1.4; CI: 1.2–1.7; p<0.001) as independent predictors
of survival. Patients with low vitamin D levels died more often from septic complications
(43%) than patients with vitamin D levels >6ng/ml (20%).
Conclusion: Extremely low serum levels of vitamin D levels are associated with increased mortality
in patients with advanced liver disease. Infectious complications are more frequent
in these patients. We speculate that a impaired immune function due to vitamin D deficiency
may explain this observation. Further studies in larger cohorts are warranted to replicate
this finding.