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Association of Early β-Amyloid Accumulation and Neuroinflammation Measured With [11C]PBR28 in Elderly Individuals Without Dementia.
- Article/chapterEnglish2021
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LIBRIS-ID:oai:gup.ub.gu.se/303573
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https://gup.ub.gu.se/publication/303573URI
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https://doi.org/10.1212/WNL.0000000000011612DOI
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http://kipublications.ki.se/Default.aspx?queryparsed=id:146818596URI
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https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-182112URI
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
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To examine whether early β-amyloid (Aβ) accumulation and metabolic risk factors are associated with neuroinflammation in elderly individuals without dementia.We examined 54 volunteers (mean age 70.0 years, 56% women, 51% APOE ɛ4 carriers) with the translocator protein (TSPO) tracer [11C]PBR28 to assess neuroinflammation and with [11C] Pittsburgh compound B (PiB) to assess cerebral Aβ accumulation. [11C]PBR28 and [11C]PiB standardized uptake value ratios (SUVRs) were quantified in 6 regions of interests by using the cerebellar cortex as a pseudo-reference and reference region, respectively. Fasting venous glucose, insulin, and high-sensitivity C-reactive protein (hs-CRP) values were determined. Homeostatic model assessment of insulin resistance (HOMA-IR) was calculated. A subset of individuals (n = 11) underwent CSF sampling, and Aβ40, Aβ42, total tau, phospho-tau, soluble TREM2, and YKL-40 levels were measured.Among the whole study group, no significant association was found between [11C]PiB and [11C]PBR28 SUVR composite scores (slope 0.02, p = 0.30). However, higher [11C]PiB binding was associated with higher [11C]PBR28 binding among amyloid-negative ([11C]PiB composite score ≤1.5) (TSPO genotype-, age- and sex-adjusted slope 0.26, p = 0.008) but not among amyloid-positive (slope -0.004, p = 0.88) participants. Higher CSF soluble TREM2 (rs = 0.72, p = 0.01) and YKL-40 (rs = 0.63, p = 0.04) concentrations were associated with a higher [11C]PBR28 composite score. Higher body mass index, HOMA-IR, and hs-CRP were associated with higher [11C]PBR28 binding in brain regions where Aβ accumulation is first detected in Alzheimer disease.While there was no association between amyloid and neuroinflammation in the overall study group, neuroinflammation was associated with amyloid among the subgroup at early stages of amyloid pathology.
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Ekblad, Laura L
(author)
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Tuisku, Jouni
(author)
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Helin, Semi
(author)
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Johansson, JarkkoUmeå universitet,Diagnostisk radiologi,Turku PET Centre, University of Turku, Finland(Swepub:umu)jajo0061
(author)
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Laine, Hanna
(author)
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Löyttyniemi, Eliisa
(author)
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Marjamäki, Päivi
(author)
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Blennow, Kaj,1958Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry(Swepub:gu)xbleka
(author)
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Zetterberg, Henrik,1973Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry(Swepub:gu)xzethe
(author)
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Jula, Antti
(author)
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Viitanen, MattiKarolinska Institutet
(author)
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Rinne, Juha O
(author)
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Umeå universitetDiagnostisk radiologi
(creator_code:org_t)
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In:Neurology: Wolters Kluwer96:121526-632X0028-3878
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Toppala, Sini
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Ekblad, Laura L
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Tuisku, Jouni
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Helin, Semi
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Johansson, Jarkk ...
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Laine, Hanna
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Löyttyniemi, Eli ...
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Marjamäki, Päivi
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Blennow, Kaj, 19 ...
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Zetterberg, Henr ...
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Jula, Antti
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Viitanen, Matti
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Rinne, Juha O
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Neurology
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