The Utility of CSF Biomarkers in Diagnosing Alzheimer’s Disease: A Thai Cohort Study

dc.contributor.authorNanthasi W.
dc.contributor.authorRattanabannakit C.
dc.contributor.authorWongkom N.
dc.contributor.authorDujada P.
dc.contributor.authorRaksthaput A.
dc.contributor.authorChaichanettee S.
dc.contributor.authorPhoyoo P.
dc.contributor.authorWachirutmanggur L.
dc.contributor.authorAn S.S.A.
dc.contributor.authorSenanarong V.
dc.contributor.correspondenceNanthasi W.
dc.contributor.otherMahidol University
dc.date.accessioned2026-01-25T18:18:21Z
dc.date.available2026-01-25T18:18:21Z
dc.date.issued2025-01-01
dc.description.abstractAbstract – Introduction: Cutoff values for cerebrospinal fluid biomarkers vary by analytic technique and population, which complicates the differentiation of Alzheimer’s disease (AD) from non-AD dementias. We aimed to establish local cerebrospinal fluid biomarker cutoffs within a Thai cohort. Materials and Methods: We recruited 68 patients with various forms of dementia from the Memory Clinic at Siriraj Hospital, Thailand. Each patient underwent clinical subtyping for dementia, and their cerebrospinal fluid levels of Aβ42, p-tau181, and t-tau were quantified using the Fujirebio INNOTEST ELISA. We then employed a data-driven approach, specifically a Z-score-based Gaussian Mixture Model, to define intersection cutoffs for Aβ42, p-tau181, t-tau, and the p-tau181/Aβ42 ratio. These established biomarker cutoffs were subsequently incorporated with clinical manifestations to refine the clinicobiological diagnoses. Results: Our study included 67 patients (mean age 65.5 ± 7.4 years, 61.2% female). Using a data-driven approach, we established the following CSF biomarker cutoffs for identifying AD in this Thai cohort: Aβ42 at 492.67 pg/mL, p-tau181 at 44.00 pg/mL, t-tau at 545.97 pg/mL, and the p-tau181/Aβ42 ratio at 0.057. After incorporating these CSF biomarker results with clinical profiles, the diagnoses changed in 17.9% of the patients. Conclusions: In this study, CSF cutoffs for differentiating AD from non-AD dementia were established through a data-driven approach, which has been demonstrated as a valid alternative methodology. The integration of clinical and biological profiles is paramount in achieving accurate dementia diagnoses.
dc.identifier.citationDementia and Geriatric Cognitive Disorders Extra Vol.15 No.1 (2025) , 162-173
dc.identifier.doi10.1159/000548539
dc.identifier.eissn16645464
dc.identifier.scopus2-s2.0-105027753782
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/114066
dc.rights.holderSCOPUS
dc.subjectNeuroscience
dc.subjectMedicine
dc.titleThe Utility of CSF Biomarkers in Diagnosing Alzheimer’s Disease: A Thai Cohort Study
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105027753782&origin=inward
oaire.citation.endPage173
oaire.citation.issue1
oaire.citation.startPage162
oaire.citation.titleDementia and Geriatric Cognitive Disorders Extra
oaire.citation.volume15
oairecerif.author.affiliationGachon University
oairecerif.author.affiliationSiriraj Hospital

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