The brain tissue growth and changes signal Alzheimer’s disease
A grape-like structure in the brain called the choroid plexus becomes enlarged and shows increased accumulation of abnormal inflammatory molecular signaling in people with Alzheimer’s disease, according to a new study. An international team of researchers, including scientists from the International Clinical Research Center (ICRC) in Brno, Czech Republic, show that these changes appear to be a more extreme or perturbed version of changes seen in the choroid plexus during normal aging.
The choroid plexus is a network of blood vessels and cells that produces cerebrospinal fluid (CSF) and creates a barrier between CSF and blood circulating throughout the body. Through the production of CSF, the choroid plexus helps maintain the brain’s immune system activation.
The choroid plexus increases in volume with age and Alzheimer’s disease. One striking finding from the study was that “the larger the choroid plexus, the poorer the cognitive performance in those Alzheimer’s patients,” said Gorazd B. Stokin, M.D., Ph.D., a leader of the Translational Neuroscience and Aging Program team at the ICRC and senior author of the study.
The scientists compared the CSF choroid plexus in healthy individuals and people with Alzheimer’s, as well as patients with other neurological diseases such as acute Lyme disease and amyotrophic lateral sclerosis or ALS. They analyzed inflammatory signaling in the CSF, as well as structure and volume changes in the choroid plexus in postmortem brains and in patients using MRI.
Following up on studies that show the choroid plexus can be damaged in aging and Alzheimer’s, Dr. Stokin and his colleagues wanted to focus more deeply on the role that this tissue may play in neuroinflammation in the disease. The researchers found protein abnormalities and “an aberrant signaling of immune molecules in the CSF and choroid plexus of people with Alzheimer’s,” said study author Patrick Pirrotte, Ph.D., Director of TGen’s Collaborative Center for Translational Mass Spectrometry in Phoenix, Arizona (US).
While these biological changes are also found in normal aging, they are different from those seen in other neurological disorders examined in the study. The changes seen in aging and Alzheimer’s patients were most pronounced in the 66-75 years old age group, the researchers found.
“The changes in choroid plexus volume in this group could be related to the recruitment of more inflammatory cells,” said Mária Čarná, Ph.D., of ICRC and the papers first author. “With the help of cognitive performance tests taken by some patients, the team also showed that increased choroid plexus volume was correlated with poorer cognitive performance.”
The scientific team has now published its findings in the prestigious journal Alzheimer’s & Dementia: The Journal of the Alzheimer’s Association. The researchers cautioned that more work needs to be done to determine whether these changes in the choroid plexus and CSF are causing Alzheimer’s, or whether they reflect the disease state.
You can access the article at:
ICRC is a joint workplace of St. Anne’s University Hospital Brno and the Faculty of Medicine of Masaryk University in Brno, Czech Republic.
Research funding for the study comes from the European Regional Development Funds (No. CZ.02.1.01/0.0/0.0/16_019/0000868 ENOCH grant); the European Union’s Horizon 2020 research and innovation programme under grant agreement (No. 857560) and CETOCOEN EXCELLENCE Teaming grant (No. CZ.02.1.01/0.0/0.0/17_043/0009632); Cetocoen Plus (CZ.02.1.01/0.0/0.0/15_003/0000469); the Czech Ministry of Health grants (NV 18-04-00346, NV 18-04-00455 and 00064203, NV19-08-00472); INBIO grant (No. CZ.02.1.01/0.0/0.0/16_026/0008451); NIH grant (P30 AGO6242); the Barrow Neurological Foundation and the Fein Foundation; the research infrastructure RECETOX grant (LM2018121); the Grant Agency of the Masaryk University (No. MUNI/G/1131/2017 GAMU grant); the National Cancer Institute of the NIH grant (No. P30CA033572); the NIA U01 grant (U01AG061357); the Next Generation EU (LX22NPO5107(MEYS)); and the Institutional Support of Excellence 2. LF UK grant (6980382).
Author: Marta Vrlová, M.A., MPH, Senior PR Specialist ICRC, email@example.com.
Contact for media: Ing. Jiří Erlebach. Head of PR and Marketing, Spokesperson, FNUSA, +420 543 182 006. firstname.lastname@example.org.