MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1097/mcg.0000000000002234

Медицинская библиотека · Journal of clinical gastroenterology · 2025

A Perfect MASH Comparing Resmetirom and GLP-1 Agonists for Metabolic-Associated Steatohepatitis: What Does the Current Evidence Suggest?

Lin Joanne, Green Victoria, Sohal Aalam, Roytman Marina

СтатьяОбзорПеревод пока не подготовлен

Аннотация

Metabolic dysfunction-associated steatotic liver disease (MASLD) has become one of the most common causes of chronic liver disease recently due to the rise of metabolic disorders such as diabetes and obesity. It will continue to have a major impact on health care systems globally given its association with cardiovascular disease and liver-related complications such as cirrhosis and hepatocellular carcinoma. In recent years, promising pharmacotherapies have emerged to address MASLD and fibrosis, such as resmetirom and glucagon-like-1 receptor agonists. There are ongoing studies to better understand resmetirom, glucagon-like-1 receptor agonists, and other possible pharmacotherapies. We discuss the current available literature on resmetirom, glucagon-like-1 receptor agonists, their safety and efficacy among patients with MASLD. Furthermore, we propose an algorithm to guide clinicians on which currently available pharmacological therapy to select for effective management of MASLD.

Для цитирования: Lin Joanne, Green Victoria, Sohal Aalam, Roytman Marina. A Perfect MASH Comparing Resmetirom and GLP-1 Agonists for Metabolic-Associated Steatohepatitis: What Does the Current Evidence Suggest?. Journal of clinical gastroenterology. 2025. DOI: 10.1097/mcg.0000000000002234.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.