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Pathophysiology, Functional Assessment and Prognostic Implications of Nutritional Disorders in Systemic Amyloidosis.
Dongiglio, Francesca; Monda, Emanuele; Palmiero, Giuseppe; Verrillo, Federica; Rubino, Marta; Diana, Gaetano; Cirillo, Annapaola; Fusco, Adelaide; Vetrano, Erica; Lioncino, Michele; Caiazza, Martina; Cerciello, Giuseppe; Capodicasa, Laura; Chiosi, Flavia; Simonelli, Vincenzo; De Rimini, Maria Luisa; Natale, Francesco; Di Santo, Alessandro; Moscarella, Elisabetta; Calabrò, Paolo; Limongelli, Giuseppe.
Afiliación
  • Dongiglio F; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Monda E; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Palmiero G; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Verrillo F; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Rubino M; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Diana G; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Cirillo A; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Fusco A; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Vetrano E; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Lioncino M; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Caiazza M; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Cerciello G; Haematology Unit, Department of Clinical Medicine and Surgery, University of Naples "Federico II", Via S. Pansini, 80131 Naples, Italy.
  • Capodicasa L; Department of Nephrology, Monaldi Hospital, Via L. Bianchi, 80131 Naples, Italy.
  • Chiosi F; Department of Ophthalmology, Monaldi Hospital, Via L. Bianchi, 80131 Naples, Italy.
  • Simonelli V; Department of Neurology, Monaldi Hospital, Via L. Bianchi, 80131 Naples, Italy.
  • De Rimini ML; Department of Nuclear Medicine, Monaldi Hospital, Via L. Bianchi, 80131 Naples, Italy.
  • Natale F; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Di Santo A; NeMO-Napoli Clinical Center for Neuromuscular Diseases, Monaldi Hospital, Via L. Bianchi, 80131 Naples, Italy.
  • Moscarella E; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Calabrò P; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
  • Limongelli G; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, 80131 Naples, Italy.
J Clin Med ; 12(2)2023 Jan 09.
Article en En | MEDLINE | ID: mdl-36675458
Gastrointestinal involvement is a common clinical feature of patients with systemic amyloidosis. This condition is responsible for invalidating gastrointestinal symptoms, a significant macro and micronutrient deficit, and is a marker of disease severity. Gastrointestinal involvement should be actively sought in patients with systemic amyloidosis, while its diagnosis is challenging in patients with isolated gastrointestinal symptoms. The nutritional status in systemic amyloidosis plays an essential role in the clinical course and is considered a significant prognostic factor. However, the definition of nutritional status is still challenging due to the lack of internationally accepted thresholds for anthropometric and biochemical variables, especially in specific populations such as those with systemic amyloidosis. This review aims to elucidate the fundamental steps for nutritional assessment by using clinical and instrumental tools for better prognostic stratification and patient management regarding quality of life and outcomes.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article País de afiliación: Italia