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Dive into the research topics where David Lahna is active.

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Featured researches published by David Lahna.


NeuroImage | 2010

GLOBAL AND LOCAL MORPHOMETRIC DIFFERENCES IN RECENTLY ABSTINENT METHAMPHETAMINE-DEPENDENT INDIVIDUALS

Daniel Schwartz; Alex Mitchell; David Lahna; Hannah S. Luber; Marilyn Huckans; Suzanne H. Mitchell; William F. Hoffman

Methamphetamine (MA) is associated with behavioral and cognitive deficits that may be related to macrostructural abnormalities. Quantitative anatomical comparisons between controls and methamphetamine-dependent individuals have produced conflicting results. We examined local and global differences in brain structure in 61 abstinent methamphetamine-dependent individuals and 44 controls with voxel-based morphometry and tissue segmentation. We related regional differences in gray matter density and whole brain segmentation volumes to performance on a behavioral measure of impulsivity and group membership using multiple linear regression. Within the MA group, we related cortical and subcortical gray matter density to length of abstinence. Controls had greater density relative to MA in bilateral insula and left middle frontal gyrus. Impulsivity was higher in the MA group and, within all subjects, impulsivity was positively correlated with gray matter density in posterior cingulate cortex and ventral striatum and negatively correlated in left superior frontal gyrus. Length of abstinence from MA was associated with greater amygdalar density. Earlier age of first use of MA (in subjects who initiated use before age 21) was associated with smaller intracranial volume. The findings are consistent with multiple possible mechanisms including neuroadaptations due to addictive behavior, neuroinflammation as well as dopaminergic and serotonergic neurotoxicity.


Neurology | 2012

Trajectory of white matter hyperintensity burden preceding mild cognitive impairment

Lisa C. Silbert; Hiroko H. Dodge; Louie Perkins; Lena Sherbakov; David Lahna; Deniz Erten-Lyons; Randall L. Woltjer; Lynne Shinto; Jeffrey Kaye

Objective: To determine the time of acceleration in white matter hyperintensity (WMH) burden, a common indicator of cerebrovascular pathology, in relation to conversion to mild cognitive impairment (MCI) in the elderly. Methods: A total of 181 cognitively intact elderly volunteers from the longitudinal, prospective, Oregon Brain Aging Study underwent yearly evaluations, including brain MRI, and cognitive testing. MRIs were analyzed for imaging markers of neurodegeneration: WMH and ventricular CSF (vCSF) volumes. The time before MCI, when the changes in WMH and vCSF burden accelerate, was assessed using a mixed-effects model with a change point for subjects who developed MCI during follow-up. Results: During a follow-up duration of up to 19.6 years, 134 subjects converted to MCI. Acceleration in %WMH volume increase occurred 10.6 years before MCI onset. On average, the annual rate of change in %WMH increased an additional 3.3% after the change point. Acceleration in %vCSF volume increase occurred 3.7 years before the onset of MCI. Out of 63 subjects who converted to MCI and had autopsy, only 28.5% had Alzheimer disease (AD) as the sole etiology of their dementia, while almost just as many (24%) had both AD and significant ischemic cerebrovascular disease present. Conclusions: Acceleration in WMH burden, a common indicator of cerebrovascular disease in the elderly, is a pathologic change that emerges early in the presymptomatic phase leading to MCI. Longitudinal changes in WMH may thus be useful in determining those at risk for cognitive impairment and for planning strategies for introducing disease-modifying therapies prior to dementia onset.


Journal of Clinical and Experimental Neuropsychology | 2011

Discounting of delayed rewards and executive dysfunction in individuals infected with hepatitis C

Marilyn Huckans; Adriana M. Seelye; Jonathan Woodhouse; Tiffany Parcel; Lisa Mull; Daniel Schwartz; Alex Mitchell; David Lahna; Amy L. Johnson; Jennifer M. Loftis; Steven Paul Woods; Suzanne H. Mitchell; William F. Hoffman

Objective: Determine whether adults with hepatitis C (HCV), regardless of substance use disorder, are more likely to discount delayed rewards than adults without hepatitis C, and explore the relationship between delay discounting and neuropsychological functioning. Methods: Procedures included clinical interviews, neuropsychological testing, and a delay discounting task. Results: Regardless of substance abuse history, adults with hepatitis C were significantly more likely to choose smaller immediate rewards over larger delayed rewards. Delay discounting correlated with performance on executive functioning tasks. Conclusions: Increased discounting is associated with broad executive dysfunction, suggesting that HCV-associated executive dysfunction may lead to altered decision-making style.


NeuroImage: Clinical | 2015

Characterizing the white matter hyperintensity penumbra with cerebral blood flow measures.

Nutta-on Promjunyakul; David Lahna; J. Kaye; Hiroko H. Dodge; Deniz Erten-Lyons; William D. Rooney; Lisa C. Silbert

Objective White matter hyperintensities (WMHs) are common with age, grow over time, and are associated with cognitive and motor impairments. Mechanisms underlying WMH growth are unclear. We aimed to determine the presence and extent of decreased normal appearing white matter (NAWM) cerebral blood flow (CBF) surrounding WMHs to identify ‘WM at risk’, or the WMH CBF penumbra. We aimed to further validate cross-sectional finding by determining whether the baseline WMH penumbra CBF predicts the development of new WMHs at follow-up. Methods Sixty-one cognitively intact elderly subjects received 3 T MPRAGE, FLAIR, and pulsed arterial spin labeling (PASL). Twenty-four subjects returned for follow-up MRI. The inter-scan interval was 18 months. A NAWM layer mask, comprised of fifteen layers, 1 mm thick each surrounding WMHs, was generated for periventricular (PVWMH) and deep (DWMH) WMHs. Mean CBF for each layer was computed. New WMH and persistent NAWM voxels for each penumbra layer were defined from follow-up MRI. Results CBF in the area surrounding WMHs was significantly lower than the total brain NAWM, extending approximately 12 mm from both the established PVWMH and DWMH. Voxels with new WMH at follow-up had significantly lower baseline CBF than voxels that maintained NAWM, suggesting that baseline CBF can predict the development of new WMHs over time. Conclusions A CBF penumbra exists surrounding WMHs, which is associated with future WMH expansion. ASL MRI can be used to monitor interventions to increase white matter blood flow for the prevention of further WM damage and its cognitive and motor consequences.


Journal of Cerebral Blood Flow and Metabolism | 2016

Comparison of cerebral blood flow and structural penumbras in relation to white matter hyperintensities: A multi-modal magnetic resonance imaging study.

Nutta On Promjunyakul; David Lahna; Jeffrey Kaye; Hiroko H. Dodge; Deniz Erten-Lyons; William D. Rooney; Lisa C. Silbert

Normal-appearing white matter (NAWM) surrounding WMHs is associated with decreased structural integrity and perfusion, increased risk of WMH growth, and is referred to as the WMH penumbra. Studies comparing structural and cerebral blood flow (CBF) penumbras within the same individuals are lacking, however, and would facilitate our understanding of mechanisms resulting in WM damage. This study aimed to compare both CBF and structural WMH penumbras in non-demented aging. Eighty-two elderly volunteers underwent 3T-MRI including fluid attenuated inversion recovery (FLAIR), pulsed arterial spin labeling and diffusion tensor imaging (DTI). A NAWM layer mask was generated for periventricular and deep WMHs. Mean CBF, DTI-fractional anisotropy (DTI-FA), DTI-mean diffusivity (DTI-MD) and FLAIR intensity for WMHs and its corresponding NAWM layer masks were computed and compared against its mean within total brain NAWM using mixed effects models. For both periventricular and deep WMHs, DTI-FA, DTI-MD and FLAIR intensity changes extended 2-9 mm surrounding WMHs (p ≤ 0.05), while CBF changes extended 13-14 mm (p ≤ 0.05). The CBF penumbra is more extensive than structural penumbras in relation to WMHs and includes WM tissue both with and without microstructural changes. Findings implicate CBF as a potential target for the prevention of both micro and macro structural WM damage.


Journal of Alzheimer's Disease | 2016

Less Daily Computer Use is Related to Smaller Hippocampal Volumes in Cognitively Intact Elderly

Lisa C. Silbert; Hiroko H. Dodge; David Lahna; Nutta On Promjunyakul; Daniel Austin; Nora Mattek; Deniz Erten-Lyons; Jeffrey Kaye

Background: Computer use is becoming a common activity in the daily life of older individuals and declines over time in those with mild cognitive impairment (MCI). The relationship between daily computer use (DCU) and imaging markers of neurodegeneration is unknown. Objective:The objective of this study was to examine the relationship between average DCU and volumetric markers of neurodegeneration on brain MRI. Methods: Cognitively intact volunteers enrolled in the Intelligent Systems for Assessing Aging Change study underwent MRI. Total in-home computer use per day was calculated using mouse movement detection and averaged over a one-month period surrounding the MRI. Spearman’s rank order correlation (univariate analysis) and linear regression models (multivariate analysis) examined hippocampal, gray matter (GM), white matter hyperintensity (WMH), and ventricular cerebral spinal fluid (vCSF) volumes in relation to DCU. A voxel-based morphometry analysis identified relationships between regional GM density and DCU. Results: Twenty-seven cognitively intact participants used their computer for 51.3 minutes per day on average. Less DCU was associated with smaller hippocampal volumes (r = 0.48, p = 0.01), but not total GM, WMH, or vCSF volumes. After adjusting for age, education, and gender, less DCU remained associated with smaller hippocampal volume (p = 0.01). Voxel-wise analysis demonstrated that less daily computer use was associated with decreased GM density in the bilateral hippocampi and temporal lobes. Conclusions: Less daily computer use is associated with smaller brain volume in regions that are integral to memory function and known to be involved early with Alzheimer’s pathology and conversion to dementia. Continuous monitoring of daily computer use may detect signs of preclinical neurodegeneration in older individuals at risk for dementia.


International Journal of Obesity | 2014

Loss of pons-to-hypothalamic white matter tracks in brainstem obesity

Jonathan Q. Purnell; David Lahna; Mary H. Samuels; William D. Rooney; W F Hoffman

Hyperphagia and obesity have been reported following damage to the hypothalamus in humans. Other brain sites are also postulated to be involved in the control of food intake and body weight regulation, such as the amygdala and brainstem. The brainstem, however, is thought to primarily integrate short-term meal-related signals but not affect long-term alterations in body weight, which is controlled by higher centers. The objective of this study was to identify structural pathways damaged in a patient with a brainstem cavernoma who experienced sudden onset of hyperphagia and >50 kg weight gain in <1 year following surgical drainage via a midline suboccipital craniotomy. Diffusion tensor imaging revealed loss of nerve fiber connections between her brainstem, hypothalamus and higher brain centers with preservation of motor tracks. Imaging and endocrine testing confirmed normal hypothalamic structure and function. Gastric bypass surgery restored normal appetite and body weight to baseline. This is the first report of ‘brainstem obesity’ and adds to the brain regions that can determine the long-term body weight set point in humans.


Alzheimers & Dementia | 2015

Less daily computer use is related to smaller hippocampal volumes in dementia-free elderly

Lisa C. Silbert; David Lahna; Hiroko H. Dodge; Nutta-on Promjunyakul; Nora Mattek; Deniz Erten-Lyons; Daniel Austin; Jeffrey Kaye

(VAN), default mode network, and dorsal attention network) was assessed using template based rotation, an approach designed for use with existing network parcellations. A linear regression model with backward elimination (p<0.1 cut-off) was utilized with the FAQ as the dependent variable and the 4 networks as the predictors of interest. Covariates included age, sex, American National Adult Reading Test intelligence quotient (AMNART IQ, a proxy of premorbid IQ), processing speed, episodic memory, and fMRI confounders (signal-to-noise ratio, movement, and bad volumes). Results:There was a significant association between greater IADL impairment and reduced FPCN connectivity (b1⁄4-29.76, partial r(pr)1⁄4-0.36, p1⁄40.03) and increased VAN connectivity (b1⁄437.44, pr1⁄40.40, p1⁄40.02). Covariates retained in the model included premorbid IQ (b1⁄40.26, pr1⁄40.42, p1⁄40.01), processing speed (b1⁄40.12, pr1⁄4-0.37, p1⁄40.03), episodic memory (b1⁄4-0.11, pr1⁄4-0.29, p1⁄40.09), and movement (b1⁄427.61, pr1⁄40.33, p1⁄40.05). The overall model was significant (p1⁄40.005) and accounted for 41% of the variance. There was no significant association with the other networks. Conclusions:These results suggest that IADL impairment inMCI relates to a complex pattern of both reduced and increased connectivity in networks spanning frontal and parietal regions. Similar findings have been reported in a study using a global functioning measure, which consists of both IADL and cognition. Furthermore, reduced FPCNconnectivity has been associatedwith greater apathy, which has been associated with IADL impairment, and increased VAN connectivity has been associated with greater executive dysfunction, which has been associated with IADL impairment.


Neurology | 2018

Baseline NAWM structural integrity and CBF predict periventricular WMH expansion over time

Nutta-on Promjunyakul; Hiroko H. Dodge; David Lahna; Erin L. Boespflug; Jeffrey Kaye; William D. Rooney; Lisa C. Silbert

Objective We aimed to describe and compare baseline cerebral blood flow (CBF) and microstructural characteristics of normal-appearing white matter (NAWM) within the vulnerable periventricular white matter hyperintensity (PVWMH) penumbra region in predicting white matter hyperintensity (WMH) growth over time. Methods Fifty-two patients, aged 82.8 years, underwent serial brain MRI, including pulsed arterial spin labeling and diffusion tensor imaging (DTI). New WMH and persistent NAWM voxels in relation to WMH penumbra at follow-up were identified. Mean baseline CBF and DTI variables of the new WMH and persistent NAWM voxels were computed. Univariate analyses with paired t tests were performed. Generalized estimating equation analyses were used to compare the relationships of baseline CBF, and structural penumbras with WMH growth, controlling for confounders. Results Low baseline CBF and fractional anisotropy, and high mean diffusivity (MD), were independently associated with new PVWMH voxels, with MD being the best predictor of WMH growth. A separate model demonstrated that radial diffusivity had the strongest relationship with WMH growth compared with CBF and axial diffusivity. Conclusion CBF and DTI measures independently predict WMH growth over time. DTI is a more sensitive predictor of WMH growth than CBF, with WMH progression likely due to demyelinating injury secondary to low perfusion. Findings support the use of MD as a sensitive marker of NAWM vulnerability in future trials aimed at preserving WM integrity.


Neurology | 2018

Nigrosome 1 absence in de novo Parkinson disease

Matthew A. Brodsky; David Lahna; Jeffrey M. Pollock; David R. Pettersson; John Grinstead; William D. Rooney

A 63-year-old man with 6 months of mild left hand rest tremor and bradykinesia and subtle left wrist cogwheel rigidity was diagnosed with idiopathic Parkinson disease (PD). The most profound neuronal degeneration in PD occurs in nigrosome 1, a lens-shaped substructure of the substantia nigra containing approximately 22,000 cell bodies in each hemi-midbrain, measuring 6 × 6 × 1 mm.1,2 A 7T MRI at the caudal level of red nucleus (figure, A) shows nigrosome 1 signal present in the left nigra and absent in the right, consistent with the clinically affected side. 7T MRI of a healthy 63-year-old with normal bilateral nigrosome 1 signal is shown for comparison (figure, B).

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