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Bawden, Stephen James; Hoad, Caroline; Kaye, Philip; Stephenson, Mary; Dolman, Grace; James, Martin W; Wilkes, Emilie; Austin, Andrew; Guha, Indra Neil; Francis, Susan; Gowland, Penny; Aithal, Guruprasad P
Comparing magnetic resonance liver fat fraction measurements with histology in fibrosis: the difference between proton density fat fraction and tissue mass fat fraction Journal Article
In: MAGMA, vol. 36, no. 4, pp. 553–563, 2023.
Abstract | Tags: Fatty liver, fibrosis, liver cirrhosis, Liver diseases, Non-alcoholic fatty liver disease
@article{Bawden2023-bk,
title = {Comparing magnetic resonance liver fat fraction measurements
with histology in fibrosis: the difference between proton
density fat fraction and tissue mass fat fraction},
author = {Stephen James Bawden and Caroline Hoad and Philip Kaye and Mary Stephenson and Grace Dolman and Martin W James and Emilie Wilkes and Andrew Austin and Indra Neil Guha and Susan Francis and Penny Gowland and Guruprasad P Aithal},
year = {2023},
date = {2023-08-01},
journal = {MAGMA},
volume = {36},
number = {4},
pages = {553\textendash563},
publisher = {Springer Science and Business Media LLC},
abstract = {OBJECTIVE: Magnetic resonance spectroscopy (MRS) provides a
powerful method of measuring fat fraction. However, previous
studies have shown that MRS results give lower values compared
with visual estimates from biopsies in fibrotic livers. This
study investigated these discrepancies and considered whether a
tissue water content correction, as assessed by MRI relaxometry,
could provide better agreement. MATERIALS AND METHODS: 110
patients were scanned in a 1.5 T Philips scanner and biopsies
were obtained. Multiple echo MRS (30 $times$ 30 $times$ 30 mm
volume) was used to determine Proton Density Fat Fraction
(PDFF). Biopsies were assessed by visual assessment for fibrosis
and steatosis grading. Digital image analysis (DIA) was also
used to quantify fat fraction within tissue samples. T1
relaxation times were then used to estimate tissue water content
to correct PDFF for confounding factors. RESULTS: PDFF values
across the four visually assessed steatosis grades were
significantly less in the higher fibrosis group (F3-F4) compared
to the lower fibrosis group (F0-F2). The slope of the linear
regression of PDFF vs DIA fat fraction was ~ 1 in the low
fibrosis group and 0.77 in the high fibrosis group. Correcting
for water content based on T1 increased the gradient but it did
not reach unity. DISCUSSION: In fibrotic livers, PDFF
underestimated fat fraction compared to DIA methods. Values were
improved by applying a water content correction, but fat
fractions were still underestimated.},
keywords = {Fatty liver, fibrosis, liver cirrhosis, Liver diseases, Non-alcoholic fatty liver disease},
pubstate = {published},
tppubtype = {article}
}
Hall, Caitlin; Gehmlich, Katja; Denning, Chris; Pavlovic, Davor
Complex relationship between cardiac fibroblasts and cardiomyocytes in health and disease Journal Article
In: J. Am. Heart Assoc., vol. 10, no. 5, pp. e019338, 2021.
Abstract | Tags: arrhythmias, cardiac fibroblasts, cardiomyocytes, fibrosis, heart failure, myofibroblast
@article{Hall2021-eq,
title = {Complex relationship between cardiac fibroblasts and
cardiomyocytes in health and disease},
author = {Caitlin Hall and Katja Gehmlich and Chris Denning and Davor Pavlovic},
year = {2021},
date = {2021-02-01},
journal = {J. Am. Heart Assoc.},
volume = {10},
number = {5},
pages = {e019338},
publisher = {Ovid Technologies (Wolters Kluwer Health)},
abstract = {Cardiac fibroblasts are the primary cell type responsible for
deposition of extracellular matrix in the heart, providing
support to the contracting myocardium and contributing to a
myriad of physiological signaling processes. Despite the
importance of fibrosis in processes of wound healing, excessive
fibroblast proliferation and activation can lead to pathological
remodeling, driving heart failure and the onset of arrhythmias.
Our understanding of the mechanisms driving the cardiac
fibroblast activation and proliferation is expanding, and
evidence for their direct and indirect effects on cardiac
myocyte function is accumulating. In this review, we focus on
the importance of the fibroblast-to-myofibroblast transition and
the cross talk of cardiac fibroblasts with cardiac myocytes. We
also consider the current use of models used to explore these
questions.},
keywords = {arrhythmias, cardiac fibroblasts, cardiomyocytes, fibrosis, heart failure, myofibroblast},
pubstate = {published},
tppubtype = {article}
}
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