Literature DB >> 25700558

There is no correlation between peripheral inflammation and cognitive status at diagnosis in Alzheimer's disease.

Adrien Julian1,2,3, Emilie Dugast4,5, Stéphanie Ragot5, Pierre Krolak-Salmon6, Gilles Berrut7, Thierry Dantoine8, Caroline Hommet9, Olivier Hanon10, Guylène Page4, Marc Paccalin11,4,5,12.   

Abstract

BACKGROUND: Besides the neurofibrillary tangles and amyloid plaques, an inflammatory process is involved at central and peripheral levels in Alzheimer's disease (AD). We aimed to determine whether peripheral inflammatory parameter levels, in plasma and in peripheral blood mononuclear cells (PBMCs), could be correlated with the cognitive status at the time of AD diagnosis.
METHODS: Patients were included at diagnosis with MMSE score between 16 and 25 and were naive of symptomatic treatment for AD. C-reactive protein >10 mg/L and any acute or chronic inflammation were considered as exclusion criteria. Cognitive assessment also included the ADAScog scale. Plasma interleukins (IL)-1β, IL-6, tumor necrosis factor (TNF)-α and the chemokine ligand 5 (CCL5) were measured using Luminex(®) X-MAP(®) technology. A subgroup of patients also underwent measures of these parameters in extracellular and intracellular compartments of PBMCs (ancillary study).
RESULTS: One hundred and nine patients were included; mean age 79.4 ± 6.8 years with 37 patients in the ancillary study. The mean values of IL-1β, TNF-α, IL-6 and CCL5 values were 1.49, 7.18, 3.09 and 69,615.81 pg/mL, respectively. No correlation between plasma cytokines or chemokine levels and cognitive scores was found. In PBMCs, the levels of cytokines were detectable but did not either show any correlation with cognitive scores.
CONCLUSION: Our data indicate that at diagnosis, peripheral levels of cytokines and CCL5 display low values without any correlation with the cognitive status. Further results of our study will show if these circulating markers are related to the progression of AD.

Entities:  

Keywords:  Alzheimer; Cognition; Inflammation; PBMC; Plasma

Mesh:

Substances:

Year:  2015        PMID: 25700558     DOI: 10.1007/s40520-015-0332-5

Source DB:  PubMed          Journal:  Aging Clin Exp Res        ISSN: 1594-0667            Impact factor:   3.636


  6 in total

1.  NFL strongly correlates with TNF-R1 in the plasma of AD patients, but not with cognitive decline.

Authors:  Constance Delaby; A Julian; G Page; S Ragot; Sylvain Lehmann; M Paccalin
Journal:  Sci Rep       Date:  2021-05-13       Impact factor: 4.379

2.  Circulating levels of monocyte chemoattractant protein-1 as a potential measure of biological age in mice and frailty in humans.

Authors:  Matthew J Yousefzadeh; Marissa J Schafer; Nicole Noren Hooten; Elizabeth J Atkinson; Michele K Evans; Darren J Baker; Ellen K Quarles; Paul D Robbins; Warren C Ladiges; Nathan K LeBrasseur; Laura J Niedernhofer
Journal:  Aging Cell       Date:  2017-12-31       Impact factor: 9.304

3.  Differential chemokine expression under the control of peripheral blood mononuclear cells issued from Alzheimer's patients in a human blood brain barrier model.

Authors:  Julie Vérité; Guylène Page; Marc Paccalin; Adrien Julian; Thierry Janet
Journal:  PLoS One       Date:  2018-08-09       Impact factor: 3.240

4.  Regulated upon activation, normal T cell expressed and secreted (RANTES) levels in the peripheral blood of patients with Alzheimer's disease.

Authors:  Gabriela Vacinova; Daniela Vejražkova; Robert Rusina; Iva Holmerová; Hana Vaňková; Eva Jarolímová; Josef Včelák; Běla Bendlová; Markéta Vaňková
Journal:  Neural Regen Res       Date:  2021-04       Impact factor: 5.135

5.  Single-cell RNA sequencing reveals B cell-related molecular biomarkers for Alzheimer's disease.

Authors:  Liu-Lin Xiong; Lu-Lu Xue; Ruo-Lan Du; Jia Liu; Chang-Yin Yu; Ting-Hua Wang; Rui-Ze Niu; Li Chen; Jie Chen; Qiao Hu; Ya-Xin Tan; Hui-Fang Shang
Journal:  Exp Mol Med       Date:  2021-12-08       Impact factor: 12.153

6.  Longitudinal chemokine profile expression in a blood-brain barrier model from Alzheimer transgenic versus wild-type mice.

Authors:  J Vérité; T Janet; D Chassaing; B Fauconneau; H Rabeony; G Page
Journal:  J Neuroinflammation       Date:  2018-06-13       Impact factor: 8.322

  6 in total

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