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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 1225A<br />

2085<br />

Neutrophil to Lymphocyte Ratio (NLR) Predicts Liver<br />

Related Death in Low MELD Cirrhotic Patients Awaiting<br />

Liver Transplant<br />

Avash Kalra 1 , Joel P. Wedd 2 , Kiran Bambha 1 , Jane Gralla 1 , Hugo<br />

R. Rosen 1 , Scott W. Biggins 1 ; 1 University of Colorado Denver,<br />

Aurora, CO; 2 Division of Digestive Diseases, Emory, Atlanta, GA<br />

MELD score has reduced accuracy in cirrhotic patients with<br />

MELD ≤20. The D’Amico 5 Stages of Cirrhosis model is a<br />

cumulative clinical staging tool and aids in identifying low<br />

MELD patients at higher risk for liver related death (Liver Transpl<br />

2014; 20:1193-1201). High (≥4, J Hepatol 2013; 58:58-64)<br />

Neutrophil to Lymphocyte Ratio (NLR) is associated with inflammatory<br />

states and may predict cirrhotic decompensation and<br />

low MELD death in cirrhosis. AIM: To evaluate the prognostic<br />

utility of high NLR (≥4) for liver related death among low MELD<br />

patients listed for liver transplant (LT), controlling for Cirrhosis<br />

Stage. METHODS: A nested case-control study was performed<br />

using adults (>17 yo) with cirrhosis awaiting LT from 2/2002-<br />

5/2011; Cases= liver related death and MELD≤20 within 90<br />

days of death; and Controls= alive for ≥90 days after LT listing.<br />

Controls were randomly chosen from all listed patients<br />

and matched (up to 3:1) to Cases by listing year, lab MELD,<br />

age, gender, and disease etiology. NLR, Cirrhosis Stage, Na,<br />

albumin, and hepatic encephalopathy (HE) were assessed at<br />

date of lowest MELD within 90 days of death for Cases and<br />

within 90 days after listing for Controls. Cirrhosis Stages are<br />

1=no varices or ascites, 2=varices, 3=variceal bleed, 4=ascites,<br />

5=ascites and variceal bleed. Conditional logistic regression<br />

was used to evaluate risk of liver related death. RESULTS:<br />

There were 41 Cases and 66 Controls; MELD scores were similar.<br />

Clinical states contributing to death in Cases were: sepsis<br />

49%, spontaneous bacterial peritonitis 15%, variceal bleeding<br />

24%, and hepatorenal syndrome 22%. NLR 25 th , 50 th , 75 th<br />

percentile cut offs were 1.9, 3.1, and 6.8. NLR was ≥4 in<br />

4/41 (59%) Cases and 14/66 (21%) Controls. Median (IQR)<br />

NLR for Cases and Controls was 5.0 (3.0-10.3) and 2.35<br />

(1.6-3.9). In univariate analysis, NLR (continuous, ≥1.9, ≥4,<br />

≥6.8), increasing Cirrhosis Stage (**categorical,1-5), variceal<br />

bleeding, large ascites, HE, Na, Albumin were significantly<br />

(p 30 ng/ml) had significantly (P = 0.009) higher daily<br />

exposure to all thresholds of lux intensities, as compared to<br />

patients with vitamin D deficiency. A seasonal comparison confirmed<br />

significantly higher lux accrued in spring and summer (P<br />

< 0.0001). Median dietary vitamin D intake (1.48 mcg/day,<br />

0.26 - 12.12) was lower than typical intakes in the general<br />

population (2 - 4 mcg). We observed no correlations between<br />

light exposure and BMI or physical activity, neither between<br />

body fat mass and serum vitamin D levels. Light intensity was<br />

the only independent predictor of serum vitamin D level in multivariate<br />

regression analysis (P = 0.004). Serum vitamin D levels<br />

were highest in patients with > 30 min exposure at > 1000<br />

lux/day (P = 0.002). Conclusions: In CLD patients, serum vitamin<br />

D levels positively correlate with light exposure but not with<br />

dietary vitamin D intake. The contribution of vitamin D from diet<br />

is minimal and below the recently revised recommendations for<br />

vitamin D intake. In contrast, our findings highlight the need<br />

for combined interventions to treat vitamin D deficiency and<br />

may guide specific recommendations for sunlight exposure in<br />

patients with CLD.<br />

Disclosures:<br />

The following authors have nothing to disclose: Elisabeth Nick, Ralf Kaiser, Frank<br />

Lammert, Caroline S. Stokes

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