| Reference : Differentially abundant transcripts in PBMC of hospitalized geriatric patients with hip ... |
| Scientific journals : Article | |||
| Human health sciences : Immunology & infectious disease Human health sciences : Geriatrics | |||
| http://hdl.handle.net/2268/87380 | |||
| Differentially abundant transcripts in PBMC of hospitalized geriatric patients with hip fracture compared to healthy aged controls | |
| English | |
| Vo, Thi Kim Duy [Facultés Universitaires Notre-Dame de la Paix - Namur - FUNDP > > Unité de recherche de biologie cellulaire > >] | |
| Godard, Patrice [Facultés Universitaires Notre-Dame de la Paix - Namur - FUNDP > > Unité de recherche de biologie cellulaire > >] | |
| de Saint-Hubert, Marie [Université Catholique de Louvain - UCL > Gériatrie Mont-Godinne > > >] | |
| Morrhaye, Gabriel [Université de Liège - ULg > Centre d'Immunologie > > >] | |
| Debacq-Chainiaux, Florence [Facultés Universitaires Notre-Dame de la Paix - Namur - FUNDP > Unité de recherche de biologie cellulaire > > >] | |
| Swine, Christian [Université Catholique de Louvain - UCL > Gériatrie - Mont Godinne > > >] | |
Geenen, Vincent [Université de Liège - ULg > > Centre d'immunologie >] | |
Martens, Henri [Université de Liège - ULg > > Centre d'immunologie >] | |
| Toussaint, Olivier [Facultés Universitaires Notre-Dame de la Paix - Namur - FUNDP > Unité de recherche de biologie cellulaire > > >] | |
| 2011 | |
| Experimental Gerontology | |
| Elsevier Science | |
| 46 | |
| 257-264 | |
| International | |
| 0531-5565 | |
| Tarrytown | |
| NY | |
| [en] Ageing ; Hip fracture ; PBMC ; Gene expression ; Inflammation ; Immunosenescence ; Oxidative stress | |
| [en] The abundance of a selection of transcript species involved in in!ammation, immunosenescence and stress
response was compared between PBMC of 35 geriatric patients with hip fracture in acute phase (days 2–4 after hospitalization) or convalescence phase (days 7–10) and 28 healthy aged controls. Twenty-nine differentially abundant transcripts were identi"ed in acute phase versus healthy ageing. Twelve of these transcripts remained differentially abundant in convalescence phase, and 22 were similarly differentially abundant in acute phase of geriatric infectious diseases. Seven of these 22 transcripts were previously identi"ed as differentially abundant in PBMC of healthy aged versus healthy young controls, with further alteration for CD28, CD69, LCK, CTSD, HMOX1, and TNFRSF1A in acute phase after geriatric hip fracture and infectious diseases. The next question is whether these alterations are common to other geriatric diseases and/or preexist before the clinical onset of the diseases. | |
| Région wallonne : Direction générale des Technologies, de la Recherche et de l'Energie - DGTRE ; Fonds de la Recherche Scientifique (Communauté française de Belgique) - F.R.S.-FNRS | |
| SENEGENE | |
| Researchers ; Professionals | |
| http://hdl.handle.net/2268/87380 | |
| 10.1016/j.exger.2010.10.012 |
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