Lab based at University of Pittsburgh interested in diagnostic and therapeutic approaches in neurodegeneration | PI: @TharickAPascoal

Pittsburgh, PA
We are pleased to announce the publication of top-line results from our HEAD study, on the comparison of tau PET tracers for the detection of tau pathology in Alzheimer’s disease, out now online in The Lancet. We are grateful to our collaborators on this work, and we look forward to continuing the dissemination of our findings from this large-scale PET comparison study. thelancet.com/journals/lance…
2
6
16
1,451
Out today in JAMA Neurology: a Pitt–Amsterdam UMC team developed a harmonized method to stage tau PET across four tracers . Our web tool guides consistent visual reads across brain regions: visualreading.unitau.app/ jamanetwork.com/journals/jam…
1
84
Two p-tau217-positive people can decline at different rates. In our new six-cohort study (n=3,505), those also GFAP-positive had 62% faster annual CDR-SB progression. GFAP may improve p-tau217 risk stratification. rdcu.be/yuJARTuqxBga @BellaverBruna
1
1
107
👇
🧠 How could plasma p-tau217 transform the way participants are pre-screened and selected for Alzheimer’s disease clinical trials? At #AAIC26, @Pamlukasewicz (of @LabPascoal) discusses how plasma biomarkers could reduce reliance on costly PET scans and enable recruitment from remote regions. 🎥 Watch the interview: ow.ly/yNi150ZFybk #Neurology #Dementia #Alzheimers #Alz
1
132
👇
At #AAIC2026, @Pamlukasewicz (of @LabPascoal) discusses a head-to-head comparison of flortaucipir and MK6240, highlighting the stronger association of plasma p-tau217 with MK6240 in early tau regions. 🎥 Watch here: ow.ly/JPJw50Zwelb #AlzheimersDisease #Dementia #Biomarkers #Tau #Neuroimaging
1
2
131
👇👇
GFAP is not just an amyloid story. In 324 Aβ− patients with vascular disease, @markley_sojr linked plasma GFAP to medial temporal atrophy and worse cognition—supporting neuroinflammation as a potential target in VCI. In Neurology: doi.org/10.1212/WNL.00000000…
2
332
Attending #AAIC2026? We’re excited to share 7 oral presentations and 16 posters at this year’s conference! Find us at the presentations below - we’d love to connect and explore opportunities for collaboration.👇
1
8
373
Pascoal Lab retweeted
Heading to #AAIC2026? Reach out to Dr Beatriz Gomez Perez-Nievas, Senior Editor at The Lancet. 🗓️ Attend the session for the LatAm-FINGERS trial on multidomain lifestyle intervention to prevent cognitive decline across Latin America – July 13, 2pm BST
2
7
21
8,192
In cognitively unimpaired Aβ+ adults, MK6240 detected medial temporal tau in 39% of participants vs 16% with flortaucipir. That's a prevalence ratio of 2.43, which translates to 23 additional cognitively unimpaired Aβ+ individuals identified as tau-positive per 100 scanned.
1
2
5
262
MK6240 was significantly better at distinguishing Alzheimer's disease from non-Alzheimer's causes of impairment. AUC 0.93 vs 0.86 for Flortaucipir. Differences were largest in the medial temporal lobe, where early tau accumulates first.
1
1
6
293
Tau PET is central to Alzheimer's diagnosis and trial selection. But does tracer choice matter? The HEAD study set out to answer that. 682 participants, both Flortaucipir and MK6240, across the Alzheimer's spectrum. Out today in @TheLancet. Article link: thelancet.com/journals/lance…
1
14
19
1,197
Pascoal Lab retweeted
🧠 New paper out in Nature Communications from the Karikari Lab @PittPsychiatry! Led by Dr. @TommyKakari, our team,@Yijun8643878478 , Xuemei Zeng & Anirudh Sehrawat, plus Pitt collaborators Drs. Kang, Pascoal, Villemagne & Cohen, developed the streamlined PAβ V2.0 assay: faster, lower-volume & more accurate blood-based Alzheimer's biomarker detection. 🎉 📖 doi.org/10.1038/s41467-026-6… #AlzheimersResearch #Biomarkers #NatureCommunications
1
1
186
We are thrilled that Dr. Pascoal was honored with the prestigious A.E. Bennett Award by the Society of Biological Psychiatry for his outstanding clinical contributions!
2
8
489
When focusing on individuals with intermediate Aβ levels, effect sizes increase and required sample sizes drop in both cognitively unimpaired and impaired groups—substantially reducing trial costs. These results support plasma p-tau217 as an efficient endpoint for AD trials.
1
92
We were very happy to receive Etienne Vachon-Presseau @evp82, Associate Professor at McGill, for a lab visit today! Etienne presented findings from analysis of UK Biobank data on prediction of chronic pain, including results from his group's recent papers (pmc.ncbi.nlm.nih.gov/article…). Thank you for the visit, Etienne!
1
7
628
Importantly, neuroinflammation alone did not predict degeneration. Its detrimental effects appeared only in the presence of Aβ or tau pathology, suggesting a context-dependent role.
1
3
97
📌 Implication: Clinical trials targeting neuroinflammation in AD could benefit from stageing participants by Aβ and tau status as inflammation can lead to opposite effects depending on the disease stage.
3
93