An association study of SERPINA1 gene polymorphisms with the risk of metabolic dysfunction-associated steatotic liver disease In an Iranian population: A preliminary case-control study DOI

S H Abdollahi,

Abbas Sahebghadam Lotfi,

Ramin Saravani

et al.

Biochemistry and Biophysics Reports, Journal Year: 2025, Volume and Issue: 42, P. 101974 - 101974

Published: March 18, 2025

Language: Английский

Metabolic-Associated Fatty Liver Disease Is Highly Prevalent in the Postacute COVID Syndrome DOI Creative Commons
Jovana Milić, S. Barbieri, Licia Gozzi

et al.

Open Forum Infectious Diseases, Journal Year: 2022, Volume and Issue: 9(3)

Published: Jan. 10, 2022

Abstract Background A proposal has recently been advanced to change the traditional definition of nonalcoholic fatty liver disease metabolic-associated (MAFLD), reflect cluster metabolic abnormalities that may be more closely associated with cardiovascular risk. Long coronavirus 2019 (COVID-19) is a smoldering inflammatory condition, characterized by several symptom clusters. This study aims determine prevalence MAFLD in patients postacute COVID syndrome (PACS) and its association other PACS-cluster phenotypes. Methods We included 235 observed at single university outpatient clinic. The diagnosis PACS was based on ≥1 symptoms: respiratory, neurocognitive, musculoskeletal, psychological, sensory, dermatological. outcome detected transient elastography during first postdischarge follow-up visit. time hospital admission calculated retrospectively using hepatic steatosis index. Results Of patients, 162 (69%) were men (median age 61). 55.3% 37.3% (P < .001). Insulin resistance (odds ratio [OR] = 1.5; 95% confidence interval [CI], 1.14–1.96), body mass index (OR 1.14; CI, 1.04–1.24), 2.54; 1.13–5.68) independent predictors MAFLD. number clusters inversely 0.86; .76–0.97). Thirty-one (13.2%) had no All correlations between weak. Conclusions Metabolic-associated highly prevalent after discharge represent specific phenotype, potential long-term health implications.

Language: Английский

Citations

30

Secondary bile acids improve risk prediction for non‐invasive identification of mild liver fibrosis in nonalcoholic fatty liver disease DOI

A‐Na Liu,

Cuifang Xu, Ya‐Ru Liu

et al.

Alimentary Pharmacology & Therapeutics, Journal Year: 2023, Volume and Issue: 57(8), P. 872 - 885

Published: Jan. 20, 2023

Dysregulated bile acid (BA) metabolism has been linked to steatosis, inflammation, and fibrosis in nonalcoholic fatty liver disease (NAFLD).

Language: Английский

Citations

20

The interplay of post-acute COVID-19 syndrome and aging: a biological, clinical and public health approach DOI
Giovanni Guaraldi, Jovana Milić, Matteo Cesari

et al.

Ageing Research Reviews, Journal Year: 2022, Volume and Issue: 81, P. 101686 - 101686

Published: July 9, 2022

Language: Английский

Citations

27

Nonalcoholic Fatty Liver Disease and Endocrine Axes—A Scoping Review DOI Creative Commons
Madalena von Hafe, Marta Borges‐Canha, Catarina Vale

et al.

Metabolites, Journal Year: 2022, Volume and Issue: 12(4), P. 298 - 298

Published: March 29, 2022

Nonalcoholic fatty liver disease (NAFLD) is the leading cause of chronic disease. NAFLD often occurs associated with endocrinopathies. Evidence suggests that endocrine dysfunction may play an important role in development, progression, and severity. Our work aimed to explore summarize crosstalk between different organs, their hormones, dysfunctions. For instance, our results show hyperprolactinemia, hypercortisolemia, polycystic ovary syndrome seem worsen NAFLD’s pathway. Hypothyroidism low growth hormone levels also contribute a bidirectional association hypercortisolism hypogonadism pathway looks likely, given current evidence. Therefore, we concluded it appears likely there link several disorders other than typically known type 2 diabetes mellitus metabolic (MS). Nevertheless, controversial insufficient evidence this area knowledge.

Language: Английский

Citations

25

Nonalcoholic fatty liver disease and osteoporosis: A potential association with therapeutic implications DOI
Ilias D. Vachliotis, Athanasios D. Anastasilakis, A. Goulas

et al.

Diabetes Obesity and Metabolism, Journal Year: 2022, Volume and Issue: 24(9), P. 1702 - 1720

Published: May 20, 2022

Nonalcoholic fatty liver disease (NAFLD) and osteoporosis are two highly prevalent metabolic diseases. Increasing experimental evidence supports a pathophysiological link between NAFLD osteoporosis. A key feature could be chronic, low-grade inflammation, which characterizes possibly affects bone metabolism. In this context, several factors, including but not limited to receptor activator of nuclear factor kappa-B ligand, osteoprotegerin, osteopontin osteocalcin, may serve as mediators. the clinical setting, most all epidemiological indicates that is associated with lower mineral density or in adults. Although an association has yet been established, thus remains speculative, pharmacological considerations already exist. Some current emerging options for have shown possible anti-osteoporotic properties (eg, vitamin E, obeticholic acid, semaglutide), while others pioglitazone, canagliflozin) increased risk fractures avoided patients concomitant osteoporosis, especially those at high fracture risk. Conversely, some medications (denosumab) might benefit NAFLD, (raloxifene) adversely affect it and, consequently, NAFLD. If medication target both diseases would great advancement. This review summarizes main on potential focuses treatment derived from association.

Language: Английский

Citations

23

Nonalcoholic Steatohepatitis Drug Development Pipeline: An Update DOI
Nicholas Chew, Cheng Han Ng, Emily Truong

et al.

Seminars in Liver Disease, Journal Year: 2022, Volume and Issue: 42(03), P. 379 - 400

Published: June 16, 2022

Nonalcoholic steatohepatitis (NASH) is a burgeoning global health crisis that mirrors the obesity pandemic. This has stimulated active research to develop novel NASH pharmacotherapies targeting dysregulated inflammatory, cellular stress, and fibrogenetic processes include (1) metabolic pathways improve insulin sensitivity, de novo lipogenesis, mitochondrial utilization of fatty acids; (2) injury or inflammatory targets reduce cell recruitment signaling; (3) liver–gut axis influence bile acid enterohepatic circulation (4) antifibrotic targets. In this review, we summarize several therapeutic agents have been studied in phase 2 3 randomized trials. addition reviewing drugs nuclear receptor pathways, liver chemokine receptors, lipid metabolism, lipotoxicity death, glucagon-like peptide-1 also discuss rationale behind use combination therapy lessons learned from unsuccessful negative clinical

Language: Английский

Citations

23

Associations of MAFLD and MAFLD subtypes with the risk of the incident myocardial infarction and stroke DOI
Chen Shen, Hongliang Xue, Rong Huang

et al.

Diabetes & Metabolism, Journal Year: 2023, Volume and Issue: 49(5), P. 101468 - 101468

Published: Aug. 14, 2023

Language: Английский

Citations

14

NAFLD: Challenges and opportunities to address the public health problem in Latin America DOI Creative Commons
Juan Pablo Arab, Luis Antonio Díaz, Melisa Dirchwolf

et al.

Annals of Hepatology, Journal Year: 2021, Volume and Issue: 24, P. 100359 - 100359

Published: May 15, 2021

Non-alcoholic fatty liver disease (NAFLD) is reaching epidemic proportions worldwide. Collectively, Latin American countries have some of the highest obesity rates in world and fastest-growing prevalence type 2 diabetes mellitus (T2DM). Since T2DM are intrinsically linked with NAFLD, epidemiological projections worrisome. In addition to this adverse setting, region America faces unique challenges obstacles addressing growing burden NAFLD. article, on occasion International NASH Day June 10, 2021, we describe main opportunities improve care people living NAFLD America. Among major be tackled are: lack awareness, limited educational for healthcare personnel general public, health system fragmentation, effective strategies prevention treatment common comorbidities, namely T2DM. Wide dissemination current concepts extensive collaboration between scientific societies, governments, non-governmental organizations, pharmaceutical industry, other stakeholders urgently needed advance public policies agenda that allows us address a whole society approach.

Language: Английский

Citations

31

Design of Hepatic Targeted Drug Delivery Systems for Natural Products: Insights into Nomenclature Revision of Nonalcoholic Fatty Liver Disease DOI
Rou Tang, Rui Li, He Li

et al.

ACS Nano, Journal Year: 2021, Volume and Issue: 15(11), P. 17016 - 17046

Published: Oct. 27, 2021

Nonalcoholic fatty liver disease (NAFLD), recently renamed metabolic-dysfunction-associated (MAFLD), affects a quarter of the worldwide population. Natural products have been extensively utilized in treating NAFLD because their distinctive advantages over chemotherapeutic drugs, despite fact that there are no approved drugs for therapy. Notably, limitations many natural products, such as poor water solubility, low bioavailability vivo, hepatic distribution, and lack targeted effects, severely restricted clinical application. These issues could be resolved via drug delivery systems (HTDDS) boost efficacy decrease adverse effects on other organs. Herein an overview comprising formulas, single medicinal plants, crude extracts has presented to treat NAFLD. Also, molecular mechanism active monomer compounds against systematically discussed. The HTDDS explored provide different nanotechnology-based treatment strategy make suggestions natural-product-based nanocarrier design. Finally, challenges opportunities put forth by nomenclature update outlined along with insights into how improve therapy design more rigorous nanocarriers HTDDS. In brief, we summarize up-to-date developments NAFLD-HTDDS based viewpoints establishment stringent anti-NAFLD natural-product-targeted nanoformulations.

Language: Английский

Citations

29

Histological assessment based on liver biopsy: the value and challenges in NASH drug development DOI Open Access

Xiaofei Tong,

Qianyi Wang, Xinyan Zhao

et al.

Acta Pharmacologica Sinica, Journal Year: 2022, Volume and Issue: 43(5), P. 1200 - 1209

Published: Feb. 14, 2022

Language: Английский

Citations

22