TY - JOUR
T1 - Differentially abundant transcripts in PBMC of hospitalized geriatric patients with hip fracture compared to healthy aged controls
AU - Vo, Thi Kim Duy
AU - Godard, Patrice
AU - de Saint-Hubert, Marie
AU - Morrhaye, Gabriel
AU - Debacq-Chainiaux, Florence
AU - Swine, Christian
AU - Geenen, Vincent
AU - Martens, Henri J.
AU - Toussaint, Olivier
PY - 2011/4/1
Y1 - 2011/4/1
N2 - The abundance of a selection of transcript species involved in inflammation, 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 identified 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 identified 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. © 2010 Elsevier Inc.
AB - The abundance of a selection of transcript species involved in inflammation, 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 identified 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 identified 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. © 2010 Elsevier Inc.
KW - Ageing
KW - Gene expression
KW - Hip fracture
KW - Immunosenescence
KW - Inflammation
KW - Oxidative stress
KW - PBMC
UR - http://www.scopus.com/inward/record.url?scp=79952699735&partnerID=8YFLogxK
U2 - 10.1016/j.exger.2010.10.012
DO - 10.1016/j.exger.2010.10.012
M3 - Article
C2 - 21074600
VL - 46
SP - 257
EP - 264
JO - Experimental Gerontology
JF - Experimental Gerontology
IS - 4
ER -