Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Aims: Metabolic dysfunction-associated steatotic liver disease (MASLD) is associated with heart failure (HF), independent of shared risk factors. Our aim was to describe the incidence of HF in patients with biopsy-proven MASLD.

Methods And Results: We followed patients with biopsy-proven MASLD from the prospective Duke NAFLD Biorepository and Clinical Database from liver biopsy (2007-2013) until death or 5 January 2023. Clinical and echocardiographic data were abstracted via manual chart review. Incident HF was defined as one of the following: (1) hospitalization for HF, (2) medical record diagnosis of HF, (3) ≥1 sign/symptom of HF and elevated natriuretic peptide, or (4) diastolic dysfunction on transthoracic echocardiography with ≥1 sign/symptom of HF. Univariable and multivariable logistic regression models were evaluated. Overall, 570 patients with biopsy-proven MASLD were included. The mean age was 49.5 years, 42.5% were male and 87.0% were non-Hispanic White. Ten patients (1.8%) had baseline HF, leaving 560 patients to assess for incident HF. Over a median follow up of 4009 days (11.0 years) (interquartile range 2270-4672 days), 100 (17.9%) patients developed incident HF while 268 (47.9%) met criteria for HF suspicion. In a multivariable model, increasing age (odds ratio [OR] 1.05, 95% confidence interval [CI] 1.02-1.08, p < 0.001) and female sex (OR 1.85, 95% CI 1.12-3.04, p = 0.02) were associated with incident HF.

Conclusions: We found a high incidence of HF in patients with biopsy-proven MASLD. Despite nearly half of patients having suspected HF, very few carried a chart diagnosis. Screening for HF in high-risk patients and establishment of formal care pathways to address early HF may reduce morbidity and mortality.

Download full-text PDF

Source
http://dx.doi.org/10.1002/ejhf.3697DOI Listing

Publication Analysis

Top Keywords

patients biopsy-proven
16
heart failure
8
metabolic dysfunction-associated
8
dysfunction-associated steatotic
8
steatotic liver
8
liver disease
8
biopsy-proven masld
8
≥1 sign/symptom
8
patients
7
incident
4

Similar Publications

Dysautonomia as a form of presentation of primary Sjögren's disease: a case series of six patients.

Immunol Res

September 2025

Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Belisario Domínguez Sección XVI, Avenida Vasco de Quiroga 15, C.P. 14080, Tlalpan, Mexico City, Mexico.

We present six patients with dysautonomia secondary to primary Sjögren's disease (pSjD) and analyze the literature regarding this topic. Case series. Patients were retrospectively recruited from a tertiary center in Mexico from 2001 to 2022 and included if they met 2016 ACR/EULAR criteria for SjD.

View Article and Find Full Text PDF

Background: Defining immunoglobulin M (IgM) nephropathy as a discrete clinical disorder remains controversial, with limited documentation in Saudi Arabian patients.

Aim: This study analyzes the clinical and pathological features, as well as the prognosis, of IgM nephropathy in the Saudi population.

Methods: This study is conducted as a retrospective descriptive study at the nephrology unit of King Saud University Medical City in Riyadh.

View Article and Find Full Text PDF

Background: Pulmonary marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALToma) is the most common form of primary pulmonary lymphoma. Data on clinic-radiologic presentation, diagnostic methods, and clinical outcome are relatively sparse.

Methods: Retrospective study of 71 patients with biopsy-proven pulmonary MALToma encountered at Mayo Clinic from 1998 to 2022.

View Article and Find Full Text PDF

Pathophysiology of Femoral Fractures in Hypophosphatasia.

Curr Osteoporos Rep

September 2025

NIHR Cambridge Biomedical Research Centre, Department of Medicine, Addenbrooke's Hospital, University of Cambridge, Cambridge, United Kingdom.

Purpose Of Review: In this review, we will examine the pathophysiology, anatomy, biochemistry, and genotype-phenotype correlation of femoral fractures in adult hypophosphatasia.

Recent Findings: Hypophosphatasia (HPP) is a rare genetic disease characterized by low activity of tissue-nonspecific alkaline phosphatase (TNAP). The disease presents a broad spectrum of clinical manifestations primarily determined by the degree of residual TNAP activity.

View Article and Find Full Text PDF

Background: Vulvar lichen sclerosus (LS) is a chronic relapsing dermatosis commonly affecting the anogenital region in postmenopausal women, though it can affect people of any age and sex. The current gold standard treatment is lifelong topical steroid application to reduce symptoms and prevent the progression of disease, causing irreversible architectural change to the vulval tissue. LS is associated with decreased quality of life and increased risk of vulvar neoplasia.

View Article and Find Full Text PDF