Abstract

Age-related disease may be mediated by low levels of chronic inflammation (“inflammaging”). Recent work suggests that gut microbes can contribute to inflammation via degradation of the intestinal barrier. While aging and age-related diseases including Alzheimer’s disease (AD) are linked to altered microbiome composition and higher levels of gut microbial components in systemic circulation, the role of intestinal inflammation remains unclear. To investigate whether greater gut inflammation is associated with advanced age and AD pathology, we assessed fecal samples from older adults to measure calprotectin, an established marker of intestinal inflammation which is elevated in diseases of gut barrier integrity. Multiple regression with maximum likelihood estimation and Satorra–Bentler corrections were used to test relationships between fecal calprotectin and clinical diagnosis, participant age, cerebrospinal fluid biomarkers of AD pathology, amyloid burden measured using 11C-Pittsburgh compound B positron emission tomography (PiB PET) imaging, and performance on cognitive tests measuring executive function and verbal learning and recall. Calprotectin levels were elevated in advanced age and were higher in participants diagnosed with amyloid-confirmed AD dementia. Additionally, among individuals with AD dementia, higher calprotectin was associated with greater amyloid burden as measured with PiB PET. Exploratory analyses indicated that calprotectin levels were also associated with cerebrospinal fluid markers of AD, and with lower verbal memory function even among cognitively unimpaired participants. Taken together, these findings suggest that intestinal inflammation is linked with brain pathology even in the earliest disease stages. Moreover, intestinal inflammation may exacerbate the progression toward AD.

Details

Title
Gut inflammation associated with age and Alzheimer’s disease pathology: a human cohort study
Author
Heston, Margo B. 1 ; Hanslik, Kendra L. 2 ; Zarbock, Katie R. 3 ; Harding, Sandra J. 1 ; Davenport-Sis, Nancy J. 1 ; Kerby, Robert L. 3 ; Chin, Nathaniel 1 ; Sun, Yi 3 ; Hoeft, Ana 1 ; Deming, Yuetiva 4 ; Vogt, Nicholas M. 1 ; Betthauser, Tobey J. 1 ; Johnson, Sterling C. 4 ; Asthana, Sanjay 1 ; Kollmorgen, Gwendlyn 5 ; Suridjan, Ivonne 6 ; Wild, Norbert 5 ; Zetterberg, Henrik 7 ; Blennow, Kaj 8 ; Rey, Federico E. 3 ; Bendlin, Barbara B. 4 ; Ulland, Tyler K. 9 

 University of Wisconsin School of Medicine and Public Health, Wisconsin Alzheimer’s Disease Research Center, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675) 
 University of Wisconsin-Madison, Department of Pathology and Laboratory Medicine, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675) 
 University of Wisconsin-Madison, Department of Bacteriology, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675) 
 University of Wisconsin School of Medicine and Public Health, Wisconsin Alzheimer’s Disease Research Center, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675); University of Wisconsin, Wisconsin Alzheimer’s Institute, School of Medicine and Public Health, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675) 
 Roche Diagnostics GmbH, Penzberg, Germany (GRID:grid.424277.0) 
 Roche Diagnostics International Ltd, Rotkreuz, Switzerland (GRID:grid.417570.0) (ISNI:0000 0004 0374 1269) 
 The Sahlgrenska Academy at the University of Gothenburg, Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Mölndal, Sweden (GRID:grid.8761.8) (ISNI:0000 0000 9919 9582); Sahlgrenska University Hospital, Clinical Neurochemistry Laboratory, Mölndal, Sweden (GRID:grid.1649.a) (ISNI:0000 0000 9445 082X); UCL Institute of Neurology, Department of Neurodegenerative Disease, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201); UK Dementia Research Institute at UCL, London, UK (GRID:grid.511435.7) (ISNI:0000 0005 0281 4208); Hong Kong Center for Neurodegenerative Diseases, Hong Kong, China (GRID:grid.24515.37) (ISNI:0000 0004 1937 1450) 
 The Sahlgrenska Academy at the University of Gothenburg, Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Mölndal, Sweden (GRID:grid.8761.8) (ISNI:0000 0000 9919 9582); Sahlgrenska University Hospital, Clinical Neurochemistry Laboratory, Mölndal, Sweden (GRID:grid.1649.a) (ISNI:0000 0000 9445 082X) 
 University of Wisconsin School of Medicine and Public Health, Wisconsin Alzheimer’s Disease Research Center, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675); University of Wisconsin-Madison, Department of Pathology and Laboratory Medicine, Madison, USA (GRID:grid.14003.36) (ISNI:0000 0001 2167 3675) 
Pages
18924
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2889800838
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.