Baseline neutrophil-to-lymphocyte ratio predicts response to corticosteroids and is associated with infection and renal dysfunction in alcoholic hepatitis.
Acute Kidney Injury
/ blood
Adrenal Cortex Hormones
/ therapeutic use
Biomarkers, Pharmacological
/ blood
Female
Hepatitis, Alcoholic
/ blood
Humans
Infections
/ blood
Leukocyte Count
Lymphocytes
/ pathology
Male
Middle Aged
Neutrophils
/ pathology
Prednisolone
/ therapeutic use
Prognosis
Retrospective Studies
Severity of Illness Index
Treatment Outcome
Journal
Alimentary pharmacology & therapeutics
ISSN: 1365-2036
Titre abrégé: Aliment Pharmacol Ther
Pays: England
ID NLM: 8707234
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
18
02
2019
revised:
13
03
2019
accepted:
14
05
2019
pubmed:
18
7
2019
medline:
16
5
2020
entrez:
18
7
2019
Statut:
ppublish
Résumé
Treating severe alcoholic hepatitis involves the exposure of patients to corticosteroids for 7 days to assess "response". To assess the prognostic and therapeutic implications of baseline neutrophil-to-lymphocyte ratio (NLR) in patients with severe alcoholic hepatitis. Patients recruited to the STOPAH trial and an independent validation group were analysed retrospectively. Area under the receiver operating curve (AUC) analysis was performed. Kaplan-Meier analysis was used to assess survival. Log-rank test and odds ratio (OR) were used for comparative analysis. Baseline NLR was available for 789 STOPAH patients. The AUC for NLR was modest for 90-day outcome (0.660), but was associated with infection, acute kidney injury (AKI) and severity of alcoholic hepatitis. Ninety-day survival was not affected by prednisolone treatment if NLR < 5 or > 8 but mortality was reduced with prednisolone treatment when the NLR was 5-8 (21.0% cf. 34.5%; P = 0.012). Prednisolone treatment increased the chance of Lille response if the NLR was ≥ 5 (56.5% cf. 41.1%: P = 0.01; OR 1.86) but increased the risk of day 7 infection (17.3% cf. 7.4%: P = 0.006; OR 2.60) and AKI (20.8% cf. 7.0%: P = 0.008; OR 3.46) if the NLR was > 8. Incorporation of NLR into a modified Glasgow alcoholic hepatitis score (mGAHS) improved the AUC to 0.783 and 0.739 for 28-day and 90-day outcome, respectively. The NLR is associated with AKI and infection in severe alcoholic hepatitis. The NLR identifies those most likely to benefit from corticosteroids at baseline (NLR 5-8). The mGAHS has a good predictive value for 28- and 90-day outcomes.
Sections du résumé
BACKGROUND
Treating severe alcoholic hepatitis involves the exposure of patients to corticosteroids for 7 days to assess "response".
AIM
To assess the prognostic and therapeutic implications of baseline neutrophil-to-lymphocyte ratio (NLR) in patients with severe alcoholic hepatitis.
METHODS
Patients recruited to the STOPAH trial and an independent validation group were analysed retrospectively. Area under the receiver operating curve (AUC) analysis was performed. Kaplan-Meier analysis was used to assess survival. Log-rank test and odds ratio (OR) were used for comparative analysis.
RESULTS
Baseline NLR was available for 789 STOPAH patients. The AUC for NLR was modest for 90-day outcome (0.660), but was associated with infection, acute kidney injury (AKI) and severity of alcoholic hepatitis. Ninety-day survival was not affected by prednisolone treatment if NLR < 5 or > 8 but mortality was reduced with prednisolone treatment when the NLR was 5-8 (21.0% cf. 34.5%; P = 0.012). Prednisolone treatment increased the chance of Lille response if the NLR was ≥ 5 (56.5% cf. 41.1%: P = 0.01; OR 1.86) but increased the risk of day 7 infection (17.3% cf. 7.4%: P = 0.006; OR 2.60) and AKI (20.8% cf. 7.0%: P = 0.008; OR 3.46) if the NLR was > 8. Incorporation of NLR into a modified Glasgow alcoholic hepatitis score (mGAHS) improved the AUC to 0.783 and 0.739 for 28-day and 90-day outcome, respectively.
CONCLUSION
The NLR is associated with AKI and infection in severe alcoholic hepatitis. The NLR identifies those most likely to benefit from corticosteroids at baseline (NLR 5-8). The mGAHS has a good predictive value for 28- and 90-day outcomes.
Substances chimiques
Adrenal Cortex Hormones
0
Biomarkers, Pharmacological
0
Prednisolone
9PHQ9Y1OLM
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
442-453Subventions
Organisme : Medical Research Council
ID : MR/R014019/1
Pays : United Kingdom
Organisme : NIHR-Imperial Biomedical Research Centre
Pays : International
Organisme : National Institute for Health Research Health Technology Assessment program
Pays : International
Organisme : MRC Stratified Medicine Grant
Pays : International
Organisme : Medical Research Council
ID : MR/M003132/1
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2019 Crown copyright. Alimentary Pharmacology and Therapeutics © 2019 John Wiley & Sons Ltd.