TY - JOUR
T1 - Changes in Serum Myostatin Levels in Alcoholic Hepatitis Correlate with Improvement in MELD
AU - Shamseddeen, Hani
AU - Madathanapalli, Abhishek
AU - Are, Vijay S.
AU - Shah, Vijay H.
AU - Sanyal, Arun J.
AU - Tang, Qing
AU - Liang, Tiebing
AU - Gelow, Kayla
AU - Zimmers, Teresa A.
AU - Chalasani, Naga
AU - Desai, Archita P.
N1 - Funding Information:
APD is funded by the American Association for the Study of Liver Disease Foundation’s 2017 Career Development Award. Collection of serum samples and serum myostatin analysis was funded by the NIH 3U01AA021840-07S1.
Publisher Copyright:
© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2021/9
Y1 - 2021/9
N2 - Background: Alcoholic hepatitis (AH) is a serious clinical syndrome often associated with muscle wasting. Myostatin, a member of the transforming growth factor-β superfamily, has been studied in diseases with muscle wasting; however, the role of myostatin in AH is unknown. Aims: To investigate the association between myostatin, clinical variables, and outcomes in AH. Methods: We analyzed data for cases of AH and controls of heavy drinkers (HD) in TREAT001 (NCT02172898) with serum myostatin levels (AH: n = 131, HD: n = 124). We compared characteristics between the two groups at baseline, 30, and 90 days and explored correlations between myostatin and clinical variables. We then modeled the relationship of myostatin to other variables, including mortality. Results: Baseline median myostatin was lower in AH compared to HD (males: 1.58 vs 3.06 ng/ml, p < 0.001; females: 0.84 vs 2.01 ng/ml, p < 0.001). In multivariable linear regression, bilirubin, WBC, and platelet count remained negatively correlated with myostatin in AH. AH females who died at 90 days had significantly lower myostatin, but in a multivariable logistic model with MELD and myostatin, only MELD remained significantly associated with 90-day mortality. During 1-year follow-up, AH cases (n = 30) demonstrated an increase in myostatin (mean, 1.73 ng/ml) which correlated with decreasing MELD scores (ρ = − 0.42, p = 0.01). Conclusions: Myostatin levels are significantly lower in AH compared to HD and are negatively correlated with total bilirubin, WBC, and platelet count. Myostatin increased as patients experienced decreases in MELD. Overall, myostatin demonstrated a dynamic relationship with AH outcomes and future studies are needed to understand the prognostic role of myostatin in AH.
AB - Background: Alcoholic hepatitis (AH) is a serious clinical syndrome often associated with muscle wasting. Myostatin, a member of the transforming growth factor-β superfamily, has been studied in diseases with muscle wasting; however, the role of myostatin in AH is unknown. Aims: To investigate the association between myostatin, clinical variables, and outcomes in AH. Methods: We analyzed data for cases of AH and controls of heavy drinkers (HD) in TREAT001 (NCT02172898) with serum myostatin levels (AH: n = 131, HD: n = 124). We compared characteristics between the two groups at baseline, 30, and 90 days and explored correlations between myostatin and clinical variables. We then modeled the relationship of myostatin to other variables, including mortality. Results: Baseline median myostatin was lower in AH compared to HD (males: 1.58 vs 3.06 ng/ml, p < 0.001; females: 0.84 vs 2.01 ng/ml, p < 0.001). In multivariable linear regression, bilirubin, WBC, and platelet count remained negatively correlated with myostatin in AH. AH females who died at 90 days had significantly lower myostatin, but in a multivariable logistic model with MELD and myostatin, only MELD remained significantly associated with 90-day mortality. During 1-year follow-up, AH cases (n = 30) demonstrated an increase in myostatin (mean, 1.73 ng/ml) which correlated with decreasing MELD scores (ρ = − 0.42, p = 0.01). Conclusions: Myostatin levels are significantly lower in AH compared to HD and are negatively correlated with total bilirubin, WBC, and platelet count. Myostatin increased as patients experienced decreases in MELD. Overall, myostatin demonstrated a dynamic relationship with AH outcomes and future studies are needed to understand the prognostic role of myostatin in AH.
KW - Alcoholism
KW - Biomarker
KW - Muscle wasting
KW - TREAT001
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U2 - 10.1007/s10620-020-06632-5
DO - 10.1007/s10620-020-06632-5
M3 - Article
C2 - 33074470
AN - SCOPUS:85092726930
SN - 0163-2116
VL - 66
SP - 3062
EP - 3073
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 9
ER -