LAV-BPIFB4 associates with reduced frailty in humans and its transfer prevents frailty progression in old mice.


Journal

Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617

Informations de publication

Date de publication:
28 08 2019
Historique:
received: 27 06 2019
accepted: 12 08 2019
pubmed: 29 8 2019
medline: 4 9 2020
entrez: 29 8 2019
Statut: ppublish

Résumé

There is an increasing concern about age-related frailty because of the growing number of elderly people in the general population. The Longevity-Associated Variant (LAV) of the human These data indicate that specific BPIFB4 haplotypes could represent useful genetic markers of frailty. In addition, horizontal transfer of a healthy gene variant can attenuate frailty in aging organisms.

Sections du résumé

BACKGROUND
There is an increasing concern about age-related frailty because of the growing number of elderly people in the general population. The Longevity-Associated Variant (LAV) of the human
CONCLUSIONS
These data indicate that specific BPIFB4 haplotypes could represent useful genetic markers of frailty. In addition, horizontal transfer of a healthy gene variant can attenuate frailty in aging organisms.

Identifiants

pubmed: 31461407
pii: 102209
doi: 10.18632/aging.102209
pmc: PMC6738439
doi:

Substances chimiques

BPIFB4 protein, human 0
Intercellular Signaling Peptides and Proteins 0
Phosphoproteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6555-6568

Subventions

Organisme : British Heart Foundation
ID : PG/18/66/33838
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Références

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Auteurs

Marco Malavolta (M)

Advanced Technology Center for Aging Research, Scientific Technological Area, IRCCS INRCA, Ancona, Italy.

Serena Dato (S)

Department of Biology, Ecology and Earth Sciences, University of Calabria, Rende, Italy.

Francesco Villa (F)

IRCCS Multimedica, Cardiovascular Department, Milan, Italy.

Francesco De Rango (F)

Department of Biology, Ecology and Earth Sciences, University of Calabria, Rende, Italy.

Francesca Iannone (F)

Department of Biology, Ecology and Earth Sciences, University of Calabria, Rende, Italy.

Anna Ferrario (A)

IRCCS Multimedica, Cardiovascular Department, Milan, Italy.

Anna Maciag (A)

IRCCS Multimedica, Cardiovascular Department, Milan, Italy.

Elena Ciaglia (E)

Department of Medicine, University of Salerno, Baronissi, Italy.

Antonio D'amato (A)

IRCCS Neuromed, Department of Vascular Physiopathology, Pozzilli, Italy.

Albino Carrizzo (A)

IRCCS Neuromed, Department of Vascular Physiopathology, Pozzilli, Italy.

Andrea Basso (A)

Advanced Technology Center for Aging Research, Scientific Technological Area, IRCCS INRCA, Ancona, Italy.

Fiorenza Orlando (F)

Experimental Animal Models for Aging Unit, Scientific Technological Area, IRCCS INRCA, Ancona, Italy.

Mauro Provinciali (M)

Advanced Technology Center for Aging Research, Scientific Technological Area, IRCCS INRCA, Ancona, Italy.
Experimental Animal Models for Aging Unit, Scientific Technological Area, IRCCS INRCA, Ancona, Italy.

Paolo Madeddu (P)

Bristol Medical School (Translational Health Sciences), Bristol Heart Institute, University of Bristol, Bristol, UK.

Giuseppe Passarino (G)

Department of Biology, Ecology and Earth Sciences, University of Calabria, Rende, Italy.

Carmine Vecchione (C)

Department of Medicine, University of Salerno, Baronissi, Italy.
IRCCS Neuromed, Department of Vascular Physiopathology, Pozzilli, Italy.

Giuseppina Rose (G)

Department of Biology, Ecology and Earth Sciences, University of Calabria, Rende, Italy.

Annibale A Puca (AA)

IRCCS Multimedica, Cardiovascular Department, Milan, Italy.
Department of Medicine, University of Salerno, Baronissi, Italy.

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Classifications MeSH