118. Non-coeliac gluten sensitivity.
Non-coeliac gluten sensitivity (NCGS) refers to individuals who report intestinal and extraintestinal symptoms related to the ingestion of gluten-based or wheat-based foods, in the absence of coeliac disease or wheat allergy. Gluten is found in multiple cereals, including wheat, rye, and barley, although the precise trigger of symptoms in NCGS remains unclear. Although approximately 10% of adults worldwide self-report gluten or wheat sensitivity, meta-analyses suggest that, during controlled challenge studies, 16-30% of these individuals have symptoms specifically triggered by gluten. However, methodological variability-including the presence of fermentable carbohydrates in challenge preparations-limits interpretation. Current evidence suggests that fermentable carbohydrates and nocebo effects contribute considerably to symptom generation in many cases. The substantial size of the gluten-free market raises questions about commercial and media influences on how NCGS is portrayed, and on the direction of related research. Definitive diagnosis of NCGS remains elusive due to the absence of biomarkers, significant overlap with disorders of gut-brain interaction, and methodological challenges in dietary evaluation. Until causative agents are identified and diagnostic tests developed, NCGS remains a diagnosis of exclusion, requiring careful systematic evaluation. Management approaches should balance dietary modification with recognition of psychological factors while ensuring nutritional adequacy. This Review critically examines current evidence regarding NCGS as a distinct entity, explores potential mechanisms, and provides practical guidance for assessment and management, while acknowledging major uncertainties in the field.
119. Semaglutide and cardiovascular outcomes by baseline and changes in adiposity measurements: a prespecified analysis of the SELECT trial.
作者: John Deanfield.;A Michael Lincoff.;Steven E Kahn.;Scott S Emerson.;Ildiko Lingvay.;Benjamin M Scirica.;Jorge Plutzky.;Robert F Kushner.;Helen M Colhoun.;G Kees Hovingh.;Signe Stensen.;Peter E Weeke.;Ole Kleist Jeppesen.;Rafael Bravo.;Chau-Chung Wu.;Issei Komuro.;Ferruccio Santini.;Jøran Hjelmesæth.;Miguel Urina-Triana.;Silvio Buscemi.;Donna H Ryan.
来源: Lancet. 2025年406卷10516期2257-2268页
The SELECT trial found semaglutide reduced major adverse cardiovascular events (MACE) in patients with overweight or obesity with cardiovascular disease but without diabetes. We report a prespecified analysis of the SELECT trial on the relationships between baseline adiposity measures, treatment-induced adiposity changes, and subsequent MACE risk.
120. Global variation in patterns of care and time to initial treatment for breast, cervical, and ovarian cancer from 2015 to 2018 (VENUSCANCER): a secondary analysis of individual records for 275 792 women from 103 population-based cancer registries in 39 countries and territories.
作者: Claudia Allemani.;Pamela Minicozzi.;Bozena Morawski.;Carlos A Lima.;Damien Bennett.;Donsuk Pongnikorn.;Dafina Petrova.;Kaire Innos.;Fabio Girardi.;Yaima Galán Alvarez.;Robin Schaffar.;Luigino Dal Maso.;Florence Molinié.;Mikhail Valkov.;Karen Phillips.;Sabine Siesling.;Annemarie Schultz.;Laetitia Daubisse-Marliac.;Rafael Marcos-Gragera.;Veronica Di Carlo.; .
来源: Lancet. 2025年406卷10517期2325-2348页
Cancers of the breast, cervix, and ovary are a major public health problem worldwide. Evaluating the consistency with clinical guidelines for treatment by use of individual high-resolution data from population-based cancer registries is a powerful tool to help interpretation of global inequalities in cancer survival. The VENUSCANCER project aims to assess the worldwide variation in patterns of care and time to initial treatment for women diagnosed with one of these three common cancers.
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