Clinical utility of 30% relative decline in MRI-PDFF in predicting fibrosis regression in non-alcoholic fatty liver disease.
Clinical utility of 30% relative decline in MRI-PDFF in predicting fibrosis regression in non-alcoholic fatty liver disease.
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DOI:
10.1136/gutjnl-2021-324264
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发表时间:
2022-05
期刊:
影响因子:
24.5
通讯作者:
Loomba R
中科院分区:
文献类型:
--
作者:
Tamaki N;Munaganuru N;Jung J;Yonan AQ;Loomba RR;Bettencourt R;Ajmera V;Valasek MA;Behling C;Sirlin CB;Loomba R
Emerging data suggest that a 30% relative decline in liver fat as assessed by magnetic resonance imaging-proton density fat fraction (MRI-PDFF) may be associated with Nonalcoholic fatty liver disease (NAFLD) Activity Score improvement, but the association between decline in MRI-PDFF and fibrosis regression is not known. Therefore, we aimed to examine the association between ≥ 30% relative decline in MRI-PDFF and fibrosis regression in NAFLD. This prospective study included 100 well-characterized patients with biopsy-proven NAFLD with paired contemporaneous MRI-PDFF assessment at two time points. MRI-PDFF response was defined as ≥ 30% relative decline in MRI-PDFF. The primary outcome was ≥1 stage histological fibrosis regression. The median (interquartile range) age was 54 (43-62) years, and body mass index was 31.9 (29-36) kg/m2. In multivariable-adjusted logistic regression analysis (adjusted for age, gender, diabetes status, race/ethnicity, interval between biopsies, gamma-glutamyl transferase, liver stiffness by magnetic resonance elastography, and change in platelet counts), MRI-PDFF response was an independent predictor of fibrosis regression with adjusted odds ratio of 6.46 (95% confidence interval: 1.1-37.0, p = 0.04). The proportion of patients with MRI-PDFF response with fibrosis regression, fibrosis no change, and fibrosis progression were 40.0%, 24.6%, and 13.0%, respectively, and the proportion of patients with MRI-PDFF response increased with fibrosis regression (p = 0.03). ≥ 30% reduction in MRI-PDFF in early phase trials can provide a useful estimate of odds of ≥ 1 stage improvement in fibrosis. These data may be helpful in sample-size estimation in nonalcoholic steatohepatitis trials.
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DOI:
10.1002/hep.26455
发表时间:
2013-12
期刊:
Hepatology (Baltimore, Md.)
影响因子:
--
作者:
Noureddin M;Lam J;Peterson MR;Middleton M;Hamilton G;Le TA;Bettencourt R;Changchien C;Brenner DA;Sirlin C;Loomba R
通讯作者:
Loomba R
影响因子:
4
作者:
Kanta J
通讯作者:
Kanta J
影响因子:
4.8
作者:
Kanda Y
通讯作者:
Kanda Y
DOI:
10.1002/hep.29797
发表时间:
2018-08
期刊:
Hepatology (Baltimore, Md.)
影响因子:
--
作者:
Caussy C;Reeder SB;Sirlin CB;Loomba R
通讯作者:
Loomba R
DOI:
10.1002/hep.29477
发表时间:
2018-05
期刊:
Hepatology (Baltimore, Md.)
影响因子:
--
作者:
Friedman SL;Ratziu V;Harrison SA;Abdelmalek MF;Aithal GP;Caballeria J;Francque S;Farrell G;Kowdley KV;Craxi A;Simon K;Fischer L;Melchor-Khan L;Vest J;Wiens BL;Vig P;Seyedkazemi S;Goodman Z;Wong VW;Loomba R;Tacke F;Sanyal A;Lefebvre E
通讯作者:
Lefebvre E