{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,13]],"date-time":"2026-07-13T14:18:39Z","timestamp":1783952319615,"version":"3.55.0"},"reference-count":27,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,7,13]],"date-time":"2026-07-13T00:00:00Z","timestamp":1783900800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,7,13]],"date-time":"2026-07-13T00:00:00Z","timestamp":1783900800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["aspenjournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Nut in Clin Prac"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>We report the case of a 23\u2010year\u2010old woman with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and preserved kidney function who was followed with a supervised plant\u2010based ketogenic diet for 11 months. The intervention was associated with a marked reduction in albuminuria (from 80 to 10\u2009mg\/g) and a stable estimated glomerular filtration rate (eGFR), with no clinically relevant metabolic or electrolyte disturbances; whereas total kidney volume increased from 617 to 709\u2009cc during follow\u2010up. This case highlights the feasibility, safety, and possible association with favorable renal biomarker changes, warranting further investigation in controlled studies in early\u2010stage ADPKD.<\/jats:p>","DOI":"10.1002\/ncp.70150","type":"journal-article","created":{"date-parts":[[2026,7,13]],"date-time":"2026-07-13T13:30:31Z","timestamp":1783949431000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Plant\u2010based ketogenic nutritional intervention in a young woman with autosomal dominant polycystic kidney disease: A case report"],"prefix":"10.1002","author":[{"given":"Paola Azucena","family":"Alvarado\u2010Pelayo","sequence":"first","affiliation":[{"name":"Department of Food and Nutrition University of Guadalajara Guadalajara M\u00e9xico"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xunaxi Nahomi","family":"Garc\u00eda\u2010Rodr\u00edguez","sequence":"additional","affiliation":[{"name":"Department of Nutrition International Ibero\u2010American University Mexico City M\u00e9xico"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Erika Fabiola","family":"G\u00f3mez\u2010Garc\u00eda","sequence":"additional","affiliation":[{"name":"Faculty of Medicine and Psychology Autonomous University of Baja California Tijuana Mexico"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0000-1945-7682","authenticated-orcid":false,"given":"Ari","family":"Cisneros\u2010Hern\u00e1ndez","sequence":"additional","affiliation":[{"name":"Faculty of Medicine University of Colima Colima Mexico"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,7,13]]},"reference":[{"issue":"10174","key":"e_1_2_8_2_1","doi-asserted-by":"crossref","first-page":"919","DOI":"10.1016\/S0140-6736(18)32782-X","article-title":"Autosomal dominant polycystic kidney disease","volume":"393","author":"Cornec\u2010Le Gall E","year":"2019","journal-title":"Lancet"},{"issue":"2","key":"e_1_2_8_3_1","doi-asserted-by":"crossref","first-page":"S1","DOI":"10.1016\/j.kint.2024.07.009","article-title":"KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD)","volume":"107","author":"Devuyst O","year":"2025","journal-title":"Kidney Int"},{"issue":"2","key":"e_1_2_8_4_1","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1016\/j.kint.2024.07.010","article-title":"KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal 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