Neurodegenerative diseases (ND) are among the leading causes of disability and mortality. Considerable sex differences exist in the occurrence of the various manifestations leading to cognitive decline. Alzheimer's disease (AD) exhibits substantial sexual dimorphisms and disproportionately affects women. Women have a higher life expectancy compared to men and, consequently, have more lifespan to develop AD. The emerging precision medicine and pharmacology concepts – taking into account the individual genetic and biological variability relevant for disease risk, prevention, detection, diagnosis, and treatment – are expected to substantially enhance our knowledge and management of AD. Stratifying the affected individuals by sex and gender is an important basic step towards personalization of scientific research, drug development, and care. We hypothesize that sex and gender differences, extending from genetic to psychosocial domains, are highly relevant for the understanding of AD pathophysiology, and for the conceptualization of basic/translational research and for clinical therapy trial design.

Precision medicine and drug development in Alzheimer's disease: the importance of sexual dimorphism and patient stratification / Hampel, Harald; Vergallo, Andrea; Giorgi, Filippo Sean; Kim, Seung Hyun; Depypere, Herman; Graziani, Manuela; Saidi, Amira; Nisticò, Robert; Lista, Simone. - In: FRONTIERS IN NEUROENDOCRINOLOGY. - ISSN 0091-3022. - ELETTRONICO. - (2018). [10.1016/j.yfrne.2018.06.001]

Precision medicine and drug development in Alzheimer's disease: the importance of sexual dimorphism and patient stratification

Graziani, Manuela;SAIDI, AMIRA;
2018

Abstract

Neurodegenerative diseases (ND) are among the leading causes of disability and mortality. Considerable sex differences exist in the occurrence of the various manifestations leading to cognitive decline. Alzheimer's disease (AD) exhibits substantial sexual dimorphisms and disproportionately affects women. Women have a higher life expectancy compared to men and, consequently, have more lifespan to develop AD. The emerging precision medicine and pharmacology concepts – taking into account the individual genetic and biological variability relevant for disease risk, prevention, detection, diagnosis, and treatment – are expected to substantially enhance our knowledge and management of AD. Stratifying the affected individuals by sex and gender is an important basic step towards personalization of scientific research, drug development, and care. We hypothesize that sex and gender differences, extending from genetic to psychosocial domains, are highly relevant for the understanding of AD pathophysiology, and for the conceptualization of basic/translational research and for clinical therapy trial design.
2018
Alzheimer's disease; biomarkers; clinical trials; gender; homeostasis; precision medicine; precision pharmacology; sex; sexual dimorphism; systems biology; endocrine and autonomic systems
01 Pubblicazione su rivista::01a Articolo in rivista
Precision medicine and drug development in Alzheimer's disease: the importance of sexual dimorphism and patient stratification / Hampel, Harald; Vergallo, Andrea; Giorgi, Filippo Sean; Kim, Seung Hyun; Depypere, Herman; Graziani, Manuela; Saidi, Amira; Nisticò, Robert; Lista, Simone. - In: FRONTIERS IN NEUROENDOCRINOLOGY. - ISSN 0091-3022. - ELETTRONICO. - (2018). [10.1016/j.yfrne.2018.06.001]
File allegati a questo prodotto
File Dimensione Formato  
Hampel_Precision-medicine_2018.pdf

solo gestori archivio

Tipologia: Documento in Post-print (versione successiva alla peer review e accettata per la pubblicazione)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 1.98 MB
Formato Adobe PDF
1.98 MB Adobe PDF   Contatta l'autore

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1120332
Citazioni
  • ???jsp.display-item.citation.pmc??? 14
  • Scopus 44
  • ???jsp.display-item.citation.isi??? 38
social impact