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The interaction between sleep-disordered breathing and apolipoprotein E genotype on cerebrospinal fluid biomarkers for Alzheimer's disease in cognitively normal elderly individuals

Osorio, Ricardo S; Ayappa, Indu; Mantua, Janna; Gumb, Tyler; Varga, Andrew; Mooney, Anne M; Burschtin, Omar E; Taxin, Zachary; During, Emmanuel; Spector, Nicole; Biagioni, Milton; Pirraglia, Elizabeth; Lau, Hiuyan; Zetterberg, Henrik; Blennow, Kaj; Lu, Shou-En; Mosconi, Lisa; Glodzik, Lidia; Rapoport, David M; de Leon, Mony J
Previous studies have suggested a link between sleep disordered breathing (SDB) and dementia risk. In the present study, we analyzed the relationship between SDB severity, cerebrospinal fluid (CSF) Alzheimer's disease-biomarkers, and the ApoE alleles. A total of 95 cognitively normal elderly participants were analyzed for SDB severity, CSF measures of phosphorylated-tau (p-tau), total-tau (t-tau), and amyloid beta 42 (Abeta-42), as well as ApoE allele status. In ApoE3+ subjects, significant differences were found between sleep groups for p-tau (F[df2] = 4.3, p = 0.017), and t-tau (F[df2] = 3.3, p = 0.043). Additionally, among ApoE3+ subjects, the apnea and/or hypopnea with 4% O2-desaturation index was positively correlated with p-tau (r = 0.30, p = 0.023), t-tau (r = 0.31, p = 0.021), and Abeta-42 (r = 0.31, p = 0.021). In ApoE2+ subjects, the apnea and/or hypopnea with 4% O2-desaturation index was correlated with lower levels of CSF Abeta-42 (r = -0.71, p = 0.004), similarly to ApoE4+ subjects where there was also a trend toward lower CSF Abeta-42 levels. Our observations suggest that there is an association between SDB and CSF Alzheimer's disease-biomarkers in cognitively normal elderly individuals. Existing therapies for SDB such as continuous positive airway pressure could delay the onset to mild cognitive impairment or dementia in normal elderly individuals.
PMCID:4022140
PMID: 24439479
ISSN: 0197-4580
CID: 851792

Mediterranean Diet and Magnetic Resonance Imaging-Assessed Brain Atrophy in Cognitively Normal Individuals at Risk for Alzheimer's Disease

Mosconi, L; Murray, J; Tsui, W H; Li, Y; Davies, M; Williams, S; Pirraglia, E; Spector, N; Osorio, R S; Glodzik, L; McHugh, P; de Leon, M J
OBJECTIVES: Epidemiological evidence linking diet, one of the most important modifiable environmental factors, and risk of Alzheimer's disease (AD) is rapidly increasing. Several studies have shown that higher adherence to a Mediterranean diet (MeDi) is associated with reduced risk of AD. This study examines the associations between high vs. lower adherence to a MeDi and structural MRI-based brain atrophy in key regions for AD in cognitively normal (NL) individuals with and without risk factors for AD. DESIGN: Cross-sectional study. SETTING: Manhattan (broader area). PARTICIPANTS: Fifty-two NL individuals (age 54+12 y, 70% women) with complete dietary information and cross-sectional, 3D T1-weighted MRI scans were examined. MEASUREMENTS: Subjects were dichotomized into those showing higher vs. lower adherences to the MeDi using published protocols. Estimates of cortical thickness for entorhinal cortex (EC), inferior parietal lobe, middle temporal gyrus, orbitofrontal cortex (OFC) and posterior cingulate cortex (PCC) were obtained by use of automated segmentation tools (FreeSurfer). Multivariate general linear models and linear regressions assessed the associations of MeDi with MRI measures. RESULTS: Of the 52 participants, 20 (39%) showed higher MeDi adherence (MeDi+) and 32 (61%) showed lower adherence (MeDi-). Groups were comparable for clinical, neuropsychological measures, presence of a family history of AD (FH), and frequency of Apolipoprotein E (APOE) epsilon4 genotype. With and without controlling for age and total intracranial volume, MeDi+ subjects showed greater thickness of AD-vulnerable ROIs as compared to MeDi- subjects (Wilk's Lambda p=0.026). Group differences were most pronounced in OFC (p=0.001), EC (p=0.03) and PCC (p=0.04) of the left hemisphere. Adjusting for gender, education, FH, APOE status, BMI, insulin resistance scores and presence of hypertension did not attenuate the relationship. CONCLUSION: NL individuals showing lower adherence to the MeDi had cortical thinning in the same brain regions as clinical AD patients compared to those showing higher adherence. These data indicate that the MeDi may have a protective effect against tissue loss, and suggest that dietary interventions may play a role in the prevention of AD.
PMCID:4165397
PMID: 25237654
ISSN: 2274-5807
CID: 1630912

FDG and Amyloid PET in Cognitively Normal Individuals at Risk for Late-Onset Alzheimer's Disease

Murray, John; Tsui, Wai H; Li, Yi; McHugh, Pauline; Williams, Schantel; Cummings, Megan; Pirraglia, Elizabeth; Solnes, Lilja; Osorio, Ricardo; Glodzik, Lidia; Vallabhajosula, Shankar; Drzezga, Alexander; Minoshima, Satoshi; de Leon, Mony J; Mosconi, Lisa
Having a parent affected by late-onset Alzheimer's disease (AD) is a major risk factor for cognitively normal (NL) individuals. This study explores the potential of PET with 18F-FDG and the amyloid- beta (Abeta) tracer 11C-Pittsburgh Compound B (PiB) for detection of individual risk in NL adults with AD-parents. METHODS: FDG- and PiB-PET was performed in 119 young to late-middle aged NL individuals including 80 NL with positive family history of AD (FH+) and 39 NL with negative family history of any dementia (FH-). The FH+ group included 50 subjects with maternal (FHm) and 30 with paternal family history (FHp). Individual FDG and PiB scans were Z scored on a voxel-wise basis relative to modality-specific reference databases using automated procedures and rated as positive or negative (+/-) for AD-typical abnormalities using predefined criteria. To determine the effect of age, the cohort was separated into younger (49 +/- 9 y) and older (68 +/- 5 y) groups relative to the median age (60 y). RESULTS: Among individuals of age >60 y, as compared to controls, NL FH+ showed a higher frequency of FDG+ scans vs. FH- (53% vs. 6% p < 0.003), and a trend for PiB+ scans (27% vs. 11%; p = 0.19). This effect was observed for both FHm and FHp groups. Among individuals of age
PMCID:4270202
PMID: 25530915
ISSN: 2161-6728
CID: 1416142

Brain imaging of cognitively normal individuals with 2 parents affected by late-onset AD

Mosconi, Lisa; Murray, John; Tsui, Wai H; Li, Yi; Spector, Nicole; Goldowsky, Alexander; Williams, Schantel; Osorio, Ricardo; McHugh, Pauline; Glodzik, Lidia; Vallabhajosula, Shankar; de Leon, Mony J
OBJECTIVES: This brain imaging study examines whether cognitively normal (NL) individuals with 2 parents affected by late-onset Alzheimer disease (LOAD) show evidence of more extensive Alzheimer disease pathology compared with those who have a single parent affected by LOAD. METHODS: Fifty-two NL individuals received MRI, (11)C-Pittsburgh compound B (PiB)-PET, and (18)F-fluoro-2-deoxyglucose (FDG)-PET. These included 4 demographically balanced groups (n = 13/group, aged 32-72 years, 60% female, 30% APOE epsilon4 carriers) of NL individuals with maternal (FHm), paternal (FHp), and maternal and paternal (FHmp) family history of LOAD, and with negative family history (FH-). Statistical parametric mapping, voxel-based morphometry, and z-score mapping were used to compare MRI gray matter volumes (GMVs), partial volume-corrected PiB retention, and FDG metabolism across FH groups and vs FH-. RESULTS: NL FHmp showed more severe abnormalities in all 3 biomarkers vs the other groups regarding the number of regions affected and magnitude of impairment. PiB retention and hypometabolism were most pronounced in FHmp, intermediate in FHm, and lowest in FHp and FH-. GMV reductions were highest in FHmp and intermediate in FHm and FHp vs FH-. In all FH+ groups, amyloid-beta deposition exceeded GMV loss and hypometabolism exceeded GMV loss (p < 0.001), while amyloid-beta deposition exceeded hypometabolism in FHmp and FHp but not in FHm. CONCLUSIONS: These biomarker findings show a "LOAD parent-dose effect" in NL individuals several years, if not decades, before possible clinical symptoms.
PMCID:3945651
PMID: 24523481
ISSN: 0028-3878
CID: 829472

Role Of Sleep In The Clearance Of Brain Waste Byproducts And The Link With Late Onset Alzheimer's Disease [Meeting Abstract]

Osorio, R. S.; Ayappa, I. A.; Gumb, T.; Varga, A.; Glodzik, L.; Rapoport, D. M.; De Leon, M. J.
ISI:000209838201579
ISSN: 1073-449x
CID: 2960102

Blood pressure decrease correlates with tau pathology and memory decline in hypertensive elderly

Glodzik, Lidia; Rusinek, Henry; Pirraglia, Elizabeth; McHugh, Pauline; Tsui, Wai; Williams, Schantel; Cummings, Megan; Li, Yi; Rich, Kenneth; Randall, Catherine; Mosconi, Lisa; Osorio, Ricardo; Murray, John; Zetterberg, Henrik; Blennow, Kaj; de Leon, Mony
In hypertension (HTN), cerebral blood flow regulation limits are changed, and the threshold for blood pressure (BP) at which perfusion is safely maintained is higher. This shift may increase the brain's vulnerability to lower BP in subjects with vascular disease. We investigated whether longitudinal reduction in mean arterial pressure (MAP) was related to changes in cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease in a group of cognitively healthy elderly with and without HTN. The relationships among MAP, memory decline, and hippocampal atrophy were also examined. Seventy-seven subjects (age 63.4 +/- 9.4, range 44-86 years; education 16.9 +/- 2.1, range 10-22 years; 60% women) were assessed twice, 2 +/- 0.5 years apart. At both time points, all subjects underwent full medical and neuropsychological evaluations, lumbar punctures, and magnetic resonance imaging examinations. Twenty-five subjects had HTN. Hyper- and normotensive subjects did not differ in their CSF biomarkers, hippocampal volumes (HipVs), or memory scores at baseline. In the entire study group, the increase in tau phosphorylated at threonine 181 (p-tau181) was associated with a decline in verbal episodic memory (beta = -0.30, p = 0.01) and HipV reduction (beta = -0.27, p = 0.02). However, longitudinal decrease in MAP was related to memory decline (beta = 0.50, p = 0.01) and an increase in p-tau181 (beta = -0.50, p = 0.01) only in subjects with HTN. Our findings suggest that the hypertensive group may be sensitive to BP reductions.
PMCID:3799812
PMID: 23969178
ISSN: 0197-4580
CID: 573802

Imaging and cerebrospinal fluid biomarkers in the search for Alzheimer's disease mechanisms

Osorio, R S; Pirraglia, E; Gumb, T; Mantua, J; Ayappa, I; Williams, S; Mosconi, L; Glodzik, L; de Leon, M J
Background: The pathophysiological process of Alzheimer's disease (AD) begins many years before the emergence of clinical symptoms (preclinical AD). A hypothetical biomarker progression in the pathogenesis of AD has been suggested, beginning with the deposition of amyloid-beta (Abeta) and followed by increases in neurofibrillary tangles, synaptic loss, hippocampal atrophy, and lastly, cognitive impairment. Objective: We explored the effect of several risk factors for AD on the pattern of AD biomarker expression in normal subjects. Methods: AD biomarker evidence was examined at baseline in 96 cognitively normal elderly subjects with none or at least one of the following: ApoE4+ allele, a maternal history of AD (mFHx), sleep-disordered breathing (SDB), and longitudinal evidence of decline to mild cognitive impairment or AD (decliners) at follow-up. Results: Decliners and ApoE4+ subjects presented with expected reduced cerebrospinal fluid Abeta42, elevated P-tau and T-tau. In addition, decliners had fluorodeoxyglucose positron emission tomography hypometabolism in the medial temporal lobe. Individuals with mFHx demonstrated no Abeta42 effect, but had elevations in P-tau and T-tau. SDB was found to be associated with elevated Abeta42, P-tau and T-tau, as well as with reduced medial temporal lobe glucose metabolic rates. Conclusion: Our results indicate a heterogeneous biomarker expression, suggesting diversity of AD pathways in at-risk presymptomatic subjects. (c) 2013 S. Karger AG, Basel.
PMCID:4022141
PMID: 24107601
ISSN: 1660-2854
CID: 806642

Imaging markers for Alzheimer disease: Which vs how

Frisoni, Giovanni B; Bocchetta, Martina; Chetelat, Gael; Rabinovici, Gil D; de Leon, Mony J; Kaye, Jeffrey; Reiman, Eric M; Scheltens, Philip; Barkhof, Frederik; Black, Sandra E; Brooks, David J; Carrillo, Maria C; Fox, Nick C; Herholz, Karl; Nordberg, Agneta; Jack, Clifford R Jr; Jagust, William J; Johnson, Keith A; Rowe, Christopher C; Sperling, Reisa A; Thies, William; Wahlund, Lars-Olof; Weiner, Michael W; Pasqualetti, Patrizio; Decarli, Charles
Revised diagnostic criteria for Alzheimer disease (AD) acknowledge a key role of imaging biomarkers for early diagnosis. Diagnostic accuracy depends on which marker (i.e., amyloid imaging, 18F-fluorodeoxyglucose [FDG]-PET, SPECT, MRI) as well as how it is measured ("metric": visual, manual, semiautomated, or automated segmentation/computation). We evaluated diagnostic accuracy of marker vs metric in separating AD from healthy and prognostic accuracy to predict progression in mild cognitive impairment. The outcome measure was positive (negative) likelihood ratio, LR+ (LR-), defined as the ratio between the probability of positive (negative) test outcome in patients and the probability of positive (negative) test outcome in healthy controls. Diagnostic LR+ of markers was between 4.4 and 9.4 and LR- between 0.25 and 0.08, whereas prognostic LR+ and LR- were between 1.7 and 7.5, and 0.50 and 0.11, respectively. Within metrics, LRs varied up to 100-fold: LR+ from approximately 1 to 100; LR- from approximately 1.00 to 0.01. Markers accounted for 11% and 18% of diagnostic and prognostic variance of LR+ and 16% and 24% of LR-. Across all markers, metrics accounted for an equal or larger amount of variance than markers: 13% and 62% of diagnostic and prognostic variance of LR+, and 29% and 18% of LR-. Within markers, the largest proportion of diagnostic LR+ and LR- variability was within 18F-FDG-PET and MRI metrics, respectively. Diagnostic and prognostic accuracy of imaging AD biomarkers is at least as dependent on how the biomarker is measured as on the biomarker itself. Standard operating procedures are key to biomarker use in the clinical routine and drug trials.
PMCID:3776529
PMID: 23897875
ISSN: 0028-3878
CID: 516552

Night-to-night variability in sleep-disordered breathing and glucose hypometabolism in cognitively normal elderly [Meeting Abstract]

Mantua, J; Ayappa, I; Glodzik, L; Tsui, W; Mosconi, L; Rapoport, D; De, Leon M; Osorio, R
Background: Glucose hypometabolism measured with FDG-PET in the medial temporal lobe (MTL) has been associated with longitudinal cognitive decline in normal elderly. Other studies find the temporal lobe may be relevant in the regulation of normal breathing, such that apneas and dyspnea are elicited with lesions and electrical stimulation in this region. Our recent work has shown that sleep-disordered breathing (S
EMBASE:71417446
ISSN: 1552-5260
CID: 953672

Postmortem study of hippocampus subfields and layers at 7T MR [Meeting Abstract]

Yazdanie, M; Ge, Y; Wadghiri, Y Z; De, Leon M; Wisniewski, T
Background: Atrophy of the hippocampus is a key pathological hallmark of Alzheimer's disease (AD). An interest of subfields of hippocampal imaging has emerged in recent years due to the advent of ultra-high field MR. This work was to evaluate the imaging parameters on human postmortem brain at 7T MR using 3D susceptibility-sensitivity imaging (SWI) with enhanced tissue susceptibility contrast to better identify these layers and hippocampal subfields that are not available on conventional MR in order to better understand the transition of the hippocampus in AD as disease progresses. Methods: Imaging was performed on a 7.0T Siemens MAGNETOM using a 24-element phased array head coil. Post-mortem brain specimens of the hippocampus were obtained from 3 patients (mean: 72.2+4.3 years) with clinically diagnosed AD and 4 age-matched healthy controls (71.4+5.2 years). Coronal brain slices were preserved and fixed in 2% agar for this study. High resolution 3D SWI was obtained with isotropic voxel size 150~320mum. For imaging optimization to better visualize amyloid plaques, we varied TR, TE, BWand flip angle from 30-100ms, 12-36ms, 60-140Hz/ pixel and 10-40degree; respectively. The SWI filtered phase images were used (multiplication factor of 4 ~ 8) to enhance susceptibility contrast in the SWI images. Results: With optimal SWI parameters TR/TE/FA of 80ms/ 20ms/30IS at 7T, Figure 1 exemplifies the excellent image contrast for visualization of hippocampal layers (Fig A) and subfields (Fig B) in an elderly post-mortem brain without AD, specifically for cell types/layers: (1) Alveus; (2) Stratum Oriens; (3) Stratum Pyramidale; (4) Stratum Radiatum; (5) Stratum Lacunosum; (6) Stratum Moleculare; and for Hippocampal Formation subfields: (1) Hippocampal Head; (2, 2') Dentate Gyrus, (3, 3') Cornu Ammonis (CA1), (4) CA2, (5) CA3, (6) Pre-Subiculum/ Subiculum, (7) Para-Subiculum, (8) Entorhinal Cortex. There was significant atrophy of the whole hippocampal formation and subfields inADsamples with lessening of the!
EMBASE:71415997
ISSN: 1552-5260
CID: 953812