Citations 648

Brain structure and cognition 3 years after the end of an early menopausal hormone therapy trial

Neurology | April 16, 2018 | Volume: 90 | Issue: 16 | Pages: No page available

10.1212/wnl.0000000000005325 | PMID 29661902

AutoVOI: real‐time automatic prescription of volume‐of‐interest for single voxel spectroscopy

Magnetic Resonance in Medicine | April 6, 2018 | Volume: 80 | Issue: 5 | Pages: 1787-1798

10.1002/mrm.27203 | PMID 29624727

PurposeTo develop a fast and automated volume‐of‐interest (VOI) prescription pipeline (AutoVOI) for single‐voxel MRS that removes the need for manual VOI placement, allows flexible VOI planning in any brain region, and enables high inter‐ and intra‐subject consistency of VOI prescription.MethodsAutoVOI was designed to transfer pre‐defined VOIs from an atlas to the 3D anatomical data of the subject during the scan. The AutoVOI pipeline was optimized for consistency in VOI placement (precision), enhanced coverage of the targeted tissue (accuracy), and fast computation speed. The tool was evaluated against manual VOI placement using existing T1‐weighted data sets and corresponding VOI prescriptions. Finally, it was implemented on 2 scanner platforms to acquire MRS data from clinically relevant VOIs that span the cerebrum, cerebellum, and the brainstem.ResultsThe AutoVOI pipeline includes skull stripping, non‐linear registration of the atlas to the subject's brain, and computation of the VOI coordinates and angulations using a minimum oriented bounding box algorithm. When compared against manual prescription, AutoVOI showed higher intra‐ and inter‐subject spatial consistency, as quantified by generalized Dice coefficients (GDC), lower intra‐ and inter‐subject variability in tissue composition (gray matter, white matter, and cerebrospinal fluid) and higher or equal accuracy, as quantified by GDC of prescribed VOI with targeted tissues. High quality spectra were obtained on Siemens and Philips 3T systems from 6 automatically prescribed VOIs by the tool.ConclusionRobust automatic VOI prescription is feasible and can help facilitate clinical adoption of MRS by avoiding operator dependence of manual selection.
Longitudinal tau PET in ageing and Alzheimer’s disease

Brain | February 22, 2018 | Volume: 141 | Issue: 5 | Pages: 1517-1528

10.1093/brain/awy059 | PMID 29538647

In vivo 18 F-AV-1451 tau PET signal in MAPT mutation carriers varies by expected tau isoforms

Neurology | February 9, 2018 | Volume: 90 | Issue: 11 | Pages: No page available

10.1212/wnl.0000000000005117 | PMID 29440563

Elevated medial temporal lobe and pervasive brain tau‐PET signal in normal participants

Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring | February 7, 2018 | Volume: 10 | Issue: 1 | Pages: 210-216

10.1016/j.dadm.2018.01.005 | PMID 29780865

AbstractIntroductionMedial temporal lobe (MTL) uptake on tau–positron emission tomography (PET) is seen not only in Alzheimer's disease (AD) dementia but also in the aging population. The relationship of these findings to the development of AD dementia needs to be better understood.MethodsTau‐PET with AV‐1451 was performed on 576 cognitively unimpaired (CU) participants aged 50–94 years. The number of CUs with and without abnormal MTL regions and those with or without extra‐MTL abnormalities was determined. Left and right regions were compared within each subject.ResultsOf CUs, 58% (334/576) had abnormal tau‐PET findings. MTL abnormalities were present in 41% (238/576) of subjects.DiscussionMTL tau‐PET signal is often associated with abnormal extra‐MTL tau‐PET signal in CU participants and may represent neurofibrillary tangle development that could identify participants most likely to develop AD dementia. Tau‐PET signal exclusively outside of the MTL is seen in 17% of CU participants and could be the initial findings in participants in different AD dementia pathways. Significant (P < .001) differences in tau–standardized uptake value ratio between sides were noted in 26 of 41 examined brain regions implicating further study of side‐specific deficits.
Hormone therapy and urine protein excretion: a multiracial cohort study, systematic review, and meta-analysis

Menopause | January 29, 2018 | Volume: 25 | Issue: 6 | Pages: 625-634

10.1097/gme.0000000000001062 | PMID 29381664

Abstract Objective: Experimental models suggest estrogen has a renoprotective effect, but human studies show variable results. Our objective was to study the association of hormone therapy (HT) and albuminuria in postmenopausal women and to synthesize the results with outcomes from prior studies. Methods: We analyzed data from postmenopausal women who participated in the second study visit (2000-2004) of the Genetic Epidemiology Network of Arteriopathy (GENOA) study. The exposure was self-reported HT use and the outcome was albuminuria (urine albumin-to-creatinine ratio >25 mg/g creatinine). We also conducted a systematic review and meta-analysis on the association of HT and urine protein in postmenopausal women. Continuous and dichotomous measures of protein excretion were converted to a standardized mean difference (SMD) for each study. Results: In the GENOA cohort ( n = 2,217), there were fewer women with albuminuria among HT users than nonusers (9% vs 19%, P < 0.001). HT use was associated with decreased odds of albuminuria (odds ratio 0.65, 95% confidence interval (CI), 0.45-0.95), after adjusting for significant differences in age, race, education, comorbidities, and the age at and cause of menopause. The SMD of the effect of HT on urine proteinuria/albuminuria in the randomized control trials ( n = 3) was 0.02 (95% CI, −0.29 to 0.33) and −0.13 (95% CI, −0.31 to 0.05) in the observational studies ( n = 9). There was significantly less albuminuria among HT users (SMD −0.15, 95% CI, −0.27 to −0.04) in the 9 studies that only reported albuminuria as an outcome and in the 10 studies with a comparator arm (SMD −0.15, 95% CI, −0.26 to −0.04). Conclusions: HT is associated with decreased odds of albuminuria, but some of the observed benefits may be related to reported outcomes, the presence of a comparator arm, and the type of study design.
Clinicopathological and 123I‐FP‐CIT SPECT correlations in patients with dementia

Annals of Clinical and Translational Neurology | January 24, 2018 | Volume: 5 | Issue: 3 | Pages: 376-381

10.1002/acn3.521 | PMID 29560382

AbstractThe relationship between clinicopathologic diagnosis and 123I‐FP‐CIT SPECT in 18 patients with dementia (12 with Lewy body disease) from one center in the United States was assessed. The sensitivity and specificity of abnormal 123I‐FP‐CIT SPECT with reduced striatal uptake on visual inspection for predicting Lewy body disease were 91.7% and 83.3%, respectively. The mean calculated putamen to occipital ratio (mPOR) based on regions of interest was significantly reduced in Lewy body disease compared to non‐Lewy body disease cases (P = 0.002). In this study, abnormal 123I‐FP‐CIT SPECT was strongly associated with underlying Lewy body disease pathology, supporting the utility of 123I‐FP‐CIT SPECT in the clinical diagnosis of dementia with Lewy bodies.
Cervical spinal cord atrophy

Neurology Neuroimmunology & Neuroinflammation | January 23, 2018 | Volume: 5 | Issue: 2 | Pages: No page available

10.1212/nxi.0000000000000435 | PMID 29435472

Sex differences in cerebrovascular pathologies on FLAIR in cognitively unimpaired elderly

Neurology | January 17, 2018 | Volume: 90 | Issue: 6 | Pages: No page available

10.1212/wnl.0000000000004913 | PMID 29343465

Association Between Microinfarcts and Blood Pressure Trajectories

JAMA Neurology | December 4, 2017 | Volume: 75 | Issue: 2 | Pages: 212

10.1001/jamaneurol.2017.3392 | PMID 29204605