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NfL reliability across laboratories, stage-dependent diagnostic performance and matrix comparability in genetic FTD: a large GENFI study

Linnemann, Christoph (author)
Wilke, Carlo (author)
Mengel, David (author)
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Zetterberg, Henrik, 1973 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Heller, Carolin (author)
Kuhle, Jens (author)
Bouzigues, Arabella (author)
Russell, Lucy L. (author)
Foster, Phoebe H. (author)
Ferry-Bolder, Eve (author)
Van Swieten, John Cornelis (author)
Jiskoot, Lize C. (author)
Seelaar, Harro (author)
Moreno, Fermin (author)
Borroni, Barbara (author)
Sanchez-Valle, Raquel (author)
Galimberti, Daniela (author)
Laforce Jr, Robert (author)
Graff, Caroline (author)
Karolinska Institutet
Masellis, Mario (author)
Tartaglia, Maria Carmela (author)
Rowe, James Benedict (author)
Finger, Elizabeth (author)
Vandenberghe, Rik (author)
de Mendonca, Alexandre (author)
Butler, Chris R. (author)
Gerhard, Alexander (author)
Ducharme, Simon (author)
Ber, Isabelle L. E. (author)
Tiraboschi, Pietro (author)
Santana, Isabel (author)
Pasquier, Florence (author)
Levin, Johannes (author)
Otto, Markus (author)
Sorbi, Sandro (author)
Rohrer, Jonathan Daniel (author)
Synofzik, Matthis (author)
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 (creator_code:org_t)
2024
2024
English.
In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. - 0022-3050 .- 1468-330X.
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BackgroundBlood neurofilament light chain (NfL) is increasingly considered as a key trial biomarker in genetic frontotemporal dementia (gFTD). We aimed to facilitate the use of NfL in gFTD multicentre trials by testing its (1) reliability across labs; (2) reliability to stratify gFTD disease stages; (3) comparability between blood matrices and (4) stability across recruiting sites.MethodsComparative analysis of blood NfL levels in a large gFTD cohort (GENFI) for (1)-(4), with n=344 samples (n=148 presymptomatic, n=11 converter, n=46 symptomatic subjects, with mutations in C9orf72, GRN or MAPT; and n=139 within-family controls), each measured in three different international labs by Simoa HD-1 analyzer.ResultsNfL revealed an excellent consistency (intraclass correlation coefficient (ICC) 0.964) and high reliability across the three labs (maximal bias (pg/mL) in Bland-Altman analysis: 1.12 +/- 1.20). High concordance of NfL across laboratories was moreover reflected by high areas under the curve for discriminating conversion stage against the (non-converting) presymptomatic stage across all three labs. Serum and plasma NfL were largely comparable (ICC 0.967). The robustness of NfL across 13 recruiting sites was demonstrated by a linear mixed effect model.ConclusionsOur results underline the suitability of blood NfL in gFTD multicentre trials, including cross-lab reliable stratification of the highly trial-relevant conversion stage, matrix comparability and cross-site robustness.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

COGNITION
FRONTOTEMPORAL DEMENTIA
NEUROPSYCHIATRY

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art (subject category)

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