Association of Choroid Plexus Volume With Serum Biomarkers, Clinical Features, and Disease Severity in Patients With Frontotemporal Lobar Degeneration Spectrum

被引:14
作者
Assogna, Martina [1 ,2 ,3 ]
Premi, Enrico [4 ]
Gazzina, Stefano [4 ]
Benussi, Alberto [4 ]
Ashton, Nicholas J. [5 ,6 ,7 ,8 ,9 ]
Zetterberg, Henrik [10 ,11 ,12 ,13 ,14 ]
Blennow, Kaj [10 ,11 ]
Gasparotti, Roberto [15 ]
Padovani, Alessandro [4 ]
Tadayon, Ehsan [16 ]
Romanella, Sara [1 ]
Sprugnoli, Giulia [1 ,17 ]
Pascual-Leone, Alvaro [18 ,19 ]
Di Lorenzo, Francesco [2 ]
Koch, Giacomo [2 ,20 ]
Borroni, Barbara [4 ]
Santarnecchi, Emiliano [1 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Gordon Ctr Med Imaging, Dept Radiol,Precis Neurosci & Neuromodulat Program, Boston, MA 02114 USA
[2] Santa Lucia Fdn IRCCS, Dept Behav & Clin Neurol, Noninvas Brain Stimulat Unit, Rome, Italy
[3] Univ Tor Vergata, Dept Syst Med, Mmory Clin, Rome, Italy
[4] Univ Brescia, Dept Clin & Expt Sci, Neurol Unit, Brescia, Italy
[5] Univ Gothenburg, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Sahlgrenska Acad, Gothenburg, Sweden
[6] Univ Gothenburg, Wallenberg Ctr Mol & Translat Med, Molndal, Sweden
[7] Kings Coll London, Inst Psychiat Psychol & Neurosci, Maurice Wohl Clin Neurosci Inst, London, England
[8] South London & Maudsley NHS Fdn, NIHR Biomed Res Ctr Mental Hlth, London, England
[9] South London & Maudsley NHS Fdn, Biomed Res Unit Dementia, London, England
[10] Univ Gothenburg, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Sahlgrenska Acad, Gothenburg, Sweden
[11] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[12] UCL Inst Neurol, Dept Neurodegenerat Dis, Queen Sq, London, England
[13] UK Dementia Res Inst UCL, London, England
[14] Hng Kong Ctr Neurodegenerat Dis, Clear Water Bay, Hong Kong, Peoples R China
[15] Univ Brescia, Neuroradiol Unit, Brescia, Italy
[16] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Berenson Allen Ctr Noninvas Brain Stimulat, Boston, MA USA
[17] Univ Siena, Dept Med Surg & Neurosci, Siena Brain Invest & Neuromodulat Lab, Siena, Italy
[18] Harvard Med Sch, Hinda & Arthur Marcus Inst Aging Res Hebrew Senior, Boston, MA USA
[19] Harvard Med Sch, Dept Neurol, Boston, MA USA
[20] Univ Ferrara, Dept Neurosci & Rehabil, Ferrara, Italy
关键词
BEHAVIORAL VARIANT; ALZHEIMERS-DISEASE; FLUID BIOMARKERS; DEMENTIA; BRAIN; SEGMENTATION; DIAGNOSIS; ASYMMETRY; RELEVANCE; CRITERIA;
D O I
10.1212/WNL.0000000000207600
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and ObjectivesChoroid plexus (ChP) is emerging as a key brain structure in the pathophysiology of neurodegenerative disorders. In this observational study, we investigated ChP volume in a large cohort of patients with frontotemporal lobar degeneration (FTLD) spectrum to explore a possible link between ChP volume and other disease-specific biomarkers.MethodsParticipants included patients meeting clinical criteria for a probable syndrome in the FTLD spectrum. Structural brain MRI imaging, serum neurofilament light (NfL), serum phosphorylated-Tau181 (p-Tau181), and cognitive and behavioral data were collected. MRI ChP volumes were obtained from an ad-hoc segmentation model based on a Gaussian Mixture Models algorithm.ResultsThree-hundred and sixteen patients within FTLD spectrum were included in this study, specifically 135 patients diagnosed with behavioral variant frontotemporal dementia (bvFTD), 75 primary progressive aphasia, 46 progressive supranuclear palsy, and 60 corticobasal syndrome. In addition, 82 age-matched healthy participants were recruited as controls (HCs). ChP volume was significantly larger in patients with FTLD compared with HC, across the clinical subtype. Moreover, we found a significant difference in ChP volume between HC and patients stratified for disease-severity based on CDR plus NACC FTLD, including patients at very early stage of the disease. Interestingly, ChP volume correlated with serum NfL, cognitive/behavioral deficits, and with patterns of cortical atrophy. Finally, ChP volume seemed to discriminate HC from patients with FTLD better than other previously identified brain structure volumes.DiscussionConsidering the clinical, pathologic, and genetic heterogeneity of the disease, ChP could represent a potential biomarker across the FTLD spectrum, especially at the early stage of disease. Further longitudinal studies are needed to establish its role in disease onset and progression.Classification of EvidenceThis study provides Class III evidence that choroid plexus volume, as measured on MRI scan, can assist in differentiating patients with FTLD from healthy controls and in characterizing disease severity.
引用
收藏
页码:E1218 / E1230
页数:13
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