Differential Associations of IL-4 With Hippocampal Subfields in Mild Cognitive Impairment and Alzheimer’s Disease

6533b85bfe1ef96bd12bac36

RESEARCH PRODUCT

Differential Associations of IL-4 With Hippocampal Subfields in Mild Cognitive Impairment and Alzheimer’s Disease

Luca Pelini Lars-olof Wahlund Christian Spenger Olof Lindberg Eric Westman Piero Floridi Bruno Vellas Roberto Tarducci Virginia Boccardi Magda Tsolaki Simon Lovestone Iwona Kłoszewska Andrew Simmons P. Chiarini J-sebastian Muehlboeck Patrizia Mecocci Hilkka Soininen

subject

0301 basic medicine Aging medicine.medical_specialty Cognitive Neuroscience Central nervous system Hippocampus Inflammation Disease Hippocampal formation Neuroprotection Alzheimer’s disease; aging; inflammation; inflammatory markers; mild cognitive impairment lcsh:RC321-571 03 medical and health sciences mild cognitive impairment 0302 clinical medicine Internal medicine medicine lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry Original Research business.industry Neurodegeneration inflammatory markers medicine.disease 030104 developmental biology Endocrinology medicine.anatomical_structure inflammation Ageing medicine.symptom business Alzheimer’s disease 030217 neurology & neurosurgery Neuroscience

description

Background/Aims: A bi-directional communication between the immune system and the central nervous system has been recently suggested. Among many cytokines, the role of IL-4 - with anti-inflammatory properties- in counteracting age-related inflammatory changes in the brain is strongly supported among studies. With this study, we aimed at investigating the association between volumetric measures of hippocampal subregions -in healthy older controls (HC), subjects affected by mild cognitive impairment (MCI) and Alzheimer’s Disease (AD)- with circulating levels of IL-4. Methods: From AddNeuroMed Project 113 HC, 101 stable MCI (sMCI), 22 converter MCI (cMCI) and 119 AD were included. Hippocampal subfield volumes were analyzed using Freesurfer 6.0.0 on high-resolution sagittal 3D-T1W MP-RAGE acquisitions. Plasmatic IL-4 was measured using ELISA assay. Results: IL-4 was found to be a) positively associate with left subiculum volume (β=0.226, p=0.037) in sMCI and b) negatively associate with left subiculum volume (β=-0.253, p=0.011) and left presubiculum volume (β=-0.257, p=0.011) in AD. Conclusion: Our results indicate a potential neuroprotective effect of IL-4 on the areas of the hippocampus more vulnerable to aging and neurodegeneration.

year	journal	country	edition	language
2019-01-17	Frontiers in Aging Neuroscience

https://doi.org/10.3389/fnagi.2018.00439