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1 NAFLD affected 24.2% of lean patients.
2 NAFLD can range in severity from steatosis to fibrotic s
3 NAFLD develops at the interface between environmental fa
4 NAFLD has a two-fold higher prevalence in HFpEF compared
5 NAFLD is associated with obesity; however, it can occur
6 NAFLD is associated with significant morbidity and morta
7 NAFLD patients had a higher frequency of advanced heart
8 NAFLD patients with evidence of nonalcoholic steatohepat
9 NAFLD was assessed using ultrasonography in the absence
10 NAFLD was diagnosed by transient elastography (TE) and d
11 NAFLD was present in 27% of the full cohort and 50% of t
12 NAFLD-associated liver complications are projected to be
13 3-10.7) or high (HR, 12.6; 95% CI, 4.3-36.3) NAFLD liver fat score, and a high NAFLD fibrosis score (
19 ns in a 3-dimensional "risk space." Although NAFLD genomics sometimes appears to be "lost in translat
21 OR, 0.96; P = .036) and a reduced risk of an NAFLD activity score of 4 or higher (ADH1B*2: OR, 0.83;
25 bserved between red meat and cholesterol and NAFLD with cirrhosis than without cirrhosis (P heterogen
27 The relationship between body mass index and NAFLD severity was significantly modified by ADH1B*2, ev
30 to ketogenic environment during obesity and NAFLD has the potential to aggravate hepatic mitochondri
37 cause of cancer-related death worldwide, and NAFLD has been identified as a rapidly emerging risk fac
41 s that have been implicated as links between NAFLD and type 2 diabetes, cardiovascular disease, and n
43 hepatic comorbidities that are influenced by NAFLD are type 2 diabetes, cardiovascular disease, and i
44 ts and scoring systems exist to characterize NAFLD and NASH, liver biopsy is the only accepted method
46 s enrol patients with histologically-defined NAFLD (non-alcoholic fatty liver disease) activity score
47 a cross-validation: a classifier to diagnose NAFLD (MRI PDFF >= 5%) and a fat fraction estimator to p
51 ecrease in nonalcoholic fatty liver disease (NAFLD) Activity Score >=2 points without worsening of fi
54 common in non-alcoholic fatty liver disease (NAFLD) and appears to also be associated with myocardial
58 lopment of nonalcoholic fatty liver disease (NAFLD) and its progression to NASH are commonly accompan
59 valence of nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH), have ste
61 jects with nonalcoholic fatty liver disease (NAFLD) and prediabetes (obese-NAFLD; n = 22).RESULTSInsu
62 he acronym nonalcoholic fatty liver disease (NAFLD) and provide suggestions on terminology that more
63 bolism and nonalcoholic fatty liver disease (NAFLD) are common in patients with human immunodeficienc
64 betes and non-alcoholic fatty liver disease (NAFLD) are increasing and may jointly become the major c
66 litus and non-alcoholic fatty liver disease (NAFLD) but studies examining the shape and content of th
67 ChREBP to nonalcoholic fatty liver disease (NAFLD) development in a mouse model for hepatic GSD 1a.
70 actors for nonalcoholic fatty liver disease (NAFLD) from population-based studies, particularly in an
71 Worldwide, nonalcoholic fatty liver disease (NAFLD) has reached epidemic proportions and in parallel,
72 eatures of nonalcoholic fatty liver disease (NAFLD) in children that relate to improvement in liver h
73 ients with nonalcoholic fatty liver disease (NAFLD) in the absence of elevated enzymes is unclear.
74 on during non-alcoholic fatty liver disease (NAFLD) include remodeling of ketogenic flux and sustaine
82 patients, nonalcoholic fatty liver disease (NAFLD) is associated with incident metabolic complicatio
96 e form of Non-alcoholic fatty liver disease (NAFLD), a chronic liver disease with a significant unmet
97 rus (HCV), nonalcoholic fatty liver disease (NAFLD), and alcohol-associated liver disease (ALD) are m
98 everity of nonalcoholic fatty liver disease (NAFLD), based on histologic analysis, compared with no a
99 creased in nonalcoholic fatty liver disease (NAFLD), but its relationship with liver inflammation is
100 ession of non-alcoholic fatty liver disease (NAFLD), but the underlying mechanisms are largely unknow
122 ups (P < .01 for all NITs in F3 and for ELF, NAFLD Fibrosis Score, Fibrosis-4 (FIB-4), and liver stif
123 val [CI]: 90%, 99%) (98 of 102) accuracy for NAFLD diagnosis (sensitivity, 97% [95% CI: 90%, 100%], 6
125 (HRs) and 95% confidence intervals (CIs) for NAFLD in association with all-cause and cause-specific m
126 algorithms that use radiofrequency data for NAFLD assessment, with MRI-derived proton density fat fr
129 he odds ratio (95% confidence intervals) for NAFLD comparing participants in the 5(th) quintile of PS
137 known NAFLD or who were suspected of having NAFLD were prospectively recruited between August 2015 a
138 4.3-36.3) NAFLD liver fat score, and a high NAFLD fibrosis score (HR, 12.2; 95% CI, 1.9-80.6) adjust
139 the U.S. population, PNPLA3 I148M and higher NAFLD liver fat and fibrosis scores were associated with
140 ifiers known to be relevant players in human NAFLD and which may determine key components of the heri
141 healthcare resources, strategies to improve NAFLD identification, staging, and promotion of lifestyl
143 ventional rodent studies (10,364 animals) in NAFLD to assess which variables influenced treatment res
153 study we define two distinct types of NI in NAFLD: inclusions bounded by the nuclear membrane, conta
157 ture on the impact of cellular senescence in NAFLD/NASH and discuss the effectiveness and safety of n
158 bariatric surgery guidelines should include NAFLD as a comorbid indication when determining eligibil
164 Materials and Methods Adults with known NAFLD or who were suspected of having NAFLD were prospec
174 ta show that enhanced ChREBP activity limits NAFLD development in GSD 1a by balancing hepatic TG prod
176 tive species are administered in three mouse NAFLD models to evaluate their effects on liver damage.
177 1 Asians with biopsy-proven NAFLD and 31 non-NAFLD controls are analyzed using 16S rRNA sequencing; a
181 fter glucose ingestion in obese-NL and obese-NAFLD is due to an increase in insulin secretion, withou
182 liver disease (NAFLD) and prediabetes (obese-NAFLD; n = 22).RESULTSInsulin sensitivity progressively
187 lt individuals with ultrasound assessment of NAFLD from the Third National Health and Nutrition Exami
191 BMP signaling is an important determinant of NAFLD in a murine model and is associated with NAFLD in
194 ffspring body composition and development of NAFLD while focusing on proteomic-based analysis of the
196 that confer high risk for the development of NAFLD: hyperglycemia, insulin resistance, and dyslipidem
200 viduals, we associated histologic markers of NAFLD severity with significant decreases in viral diver
202 igh-cholesterol diet-induced rodent model of NAFLD, we observed a progressive stepwise reduction in t
205 tes per week) demonstrated 40% lower odds of NAFLD, whereas transportation-related PA was associated
206 In the race-specific analysis, the PAFs of NAFLD for all-cause mortality (9.3%; 95% CI, 4.0, 14.6)
208 selected variants in the pathophysiology of NAFLD and highlight opportunities for future clinical re
212 tween perceived stress and the prevalence of NAFLD in a large sample of apparently healthy men and wo
214 y associated with an increased prevalence of NAFLD, supporting a possible relationship between percei
217 stronger association with risk reduction of NAFLD in women, women showed a lower tendency of meeting
219 ribed adaptations underlying the reversal of NAFLD by KD: That is, markedly altered hepatic mitochond
228 atients without this inflammatory subtype of NAFLD, with annual all-cause mortality rate of 25.56 per
232 argets across multiple pathways that promote NAFLD development and influence several progressive outc
233 me profiles of 171 Asians with biopsy-proven NAFLD and 31 non-NAFLD controls are analyzed using 16S r
234 ultiethnic adult patients with biopsy-proven NAFLD enrolled into 4 different studies conducted by the
235 as performed in a cohort of 83 biopsy-proven NAFLD patients and 13 patients with non-invasively diagn
236 02 patients (62.7% women) with biopsy-proven NAFLD who underwent contemporaneous MRE and liver biopsy
237 chia coli LPS in patients with biopsy-proven NAFLD, 25 simple steatosis (nonalcoholic fatty liver) an
243 o identify additional biomarkers to stratify NAFLD patients without cirrhosis who are at risk for HCC
249 vival rates were significantly higher in the NAFLD-HCC cases compared to HBV-HCC (HR = 0.35, 95% CI 0
252 hydroxysteroid 17-beta dehydrogenase 13) to NAFLD and expand the associated underlying mechanisms us
254 We examined dietary factors in relation to NAFLD risk in African Americans, Japanese Americans, Lat
258 erative liver biopsies were classified using NAFLD activity score (NAS) and steatosis, activity and f
260 ndex (BMI) was independently associated with NAFLD (aOR 1.2 95% CI 1.08-1.34), and type 2 diabetes wa
261 ry factors are independently associated with NAFLD and NAFLD-related cirrhosis in a multiethnic popul
264 ndividuals have risk factors associated with NAFLD, but the majority do not develop advanced liver di
265 005) intakes were positively associated with NAFLD, while dietary fiber intake (P trend = 0.003) was
270 taging and clinical features correlated with NAFLD among patients with heart failure with preserved e
271 pe of PA remained stable in individuals with NAFLD except for a downtrend in transportation-related P
275 reased mortality risk among individuals with NAFLD; therefore, the population attributable fractions
276 dy was performed for adult participants with NAFLD and control participants without liver disease.
277 lassifier to differentiate participants with NAFLD versus participants without NAFLD and a fat fracti
278 a study of fecal viromes from patients with NAFLD and control individuals, we associated histologic
280 review addressing HCC risk in patients with NAFLD and provide Best Practice Advice statements to add
281 R55 expression in the liver of patients with NAFLD compared with individuals without obesity and with
282 tile range, 26.5-50.7 months), patients with NAFLD had higher incidences of diabetes (4.74 [95% confi
284 addressing HCC surveillance in patients with NAFLD outside the context of established cirrhosis.
285 inicians with respect to which patients with NAFLD should undergo HCC surveillance, optimal screening
286 velopment of cirrhosis between patients with NAFLD who underwent bariatric surgery and a well-matched
298 n among those who were lean patients without NAFLD (61.9% vs 48.9% and 36.7% vs 24.2%, respectively).