| Reference : Transcriptomic biomarkers of the response of hospitalized geriatric patients admitted wi... |
| Scientific journals : Article | |||
| Human health sciences : Immunology & infectious disease Human health sciences : Geriatrics | |||
| http://hdl.handle.net/2268/87495 | |||
| Transcriptomic biomarkers of the response of hospitalized geriatric patients admitted with heart failure. Comparison to hospitalized geriatric patients with infectious diseases or hip fracture | |
| English | |
| Vo, Thi Kim Duy [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 > > >] | |
| Godard, Patrice [Facultés Universitaires Notre-Dame de la Paix - Namur - FUNDP > Unité de recherche de biologie cellulaire > > >] | |
Geenen, Vincent [Université de Liège - ULg > > Centre d'immunologie >] | |
Martens, Henri [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 > > >] | |
| Toussaint, Olivier [Facultés Universitaires Notre-Dame de la Paix - Namur - FUNDP > Unité de recherche de biologie cellulaire > > >] | |
| 2011 | |
| Mechanisms of Ageing & Development | |
| Elsevier Science Ireland | |
| 132 | |
| 131-139 | |
| International | |
| 0047-6374 | |
| Limerick | |
| Ireland | |
| [en] Ageing ; Gene expression ; Heart failure ; Inflammation ; Immunosenescence ; Oxidative stress | |
| [en] The abundance of a preselection of transcripts involved in inflammation, immunosenescence and stress
response was compared between PBMC of healthy aged donors and aged patients in acute phase of heart failure and at recovery. This study identified 22 transcripts differentially abundant in acute phase of heart failure versus healthy aged subjects. Transcripts involved in inflammation and oxidative stress weremore abundant. Those associated with T-cell functions were less abundant. The results were compared to two other major acute geriatric issues: infectious diseases and hip fracture. In acute phase, compared to healthy aged subjects, the abundance of 15/22 transcripts was also altered in both geriatric infectious diseases and hip fracture. Many variations had not vanished at the recovery phase. The abundance of CD28, CD69, LCK, HMOX1, TNFRSF1A transcripts, known to be altered in healthy aged versus healthy young subjects, was further affected in acute phase of the three geriatric diseases considered. The transcript levels of BCL2, CASP8, CCL5, DDIT3, EGR3, IL10RB, IL1R2, SERPINB2 and TIMP1 were affected in all three pathological conditions compared to healthy aged, but not versus healthy young subjects. In conclusion, this work provides critical targets for therapeutic research on geriatric heart failure, infectious diseases and hip fracture. | |
| 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/2268/87495 | |
| 10.1016/j.mad.2011.02.002 |
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