Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 16 de 16
Filter
1.
Front Neurol ; 8: 127, 2017.
Article in English | MEDLINE | ID: mdl-28484418

ABSTRACT

The long-term effects of blast exposure are a major health concern for combat veterans returning from the recent conflicts in Iraq and Afghanistan. We used an optimized diffusion tensor imaging tractography algorithm to assess white matter (WM) fractional anisotropy (FA) in blast-exposed Iraq and Afghanistan veterans (n = 40) scanned on average 3.7 years after deployment/trauma exposure. Veterans diagnosed with a blast-related mild traumatic brain injury (mTBI) were compared to combat veterans with blast exposure but no TBI diagnosis. Blast exposure was associated with decreased FA in several WM tracts. However, total blast exposure did not correlate well with neuropsychological testing performance and there were no differences in FA based on mTBI diagnosis. Yet, veterans with mTBI performed worse on every neurocognitive test administered. Multiple linear regression across all blast-exposed veterans using a six-factor prediction model indicated that the amount of blast exposure accounted for 11-15% of the variability in composite FA scores such that as blast exposure increased, FA decreased. Education accounted for 10% of the variability in composite FA scores and 25-32% of FA variability in the right cingulum, such that as level of education increased, FA increased. Total blast exposure, age, and education were significant predictors of FA in the left cingulum. We did not find any effect of post-traumatic stress disorder on cognition or composite FA. In summary, our findings suggest that greater total blast exposure is a contributing factor to poor WM integrity. While FA was not associated with neurocognitive performance, we hypothesize that FA changes in the cingulum in veterans with multiple combat exposures and no head trauma prior to deployment may represent a marker of vulnerability for future deficits. Future work needs to examine this longitudinally.

2.
Mol Neurodegener ; 9: 10, 2014 Feb 03.
Article in English | MEDLINE | ID: mdl-24484858

ABSTRACT

BACKGROUND: Identification and quantification of fibrillar amyloid in brain using positron emission tomography (PET) imaging and Amyvid™ ([18 F] Amyvid, [18 F] florbetapir, 18 F-AV-45) was recently approved by the US Food and Drug Administration as a clinical tool to estimate brain amyloid burden in patients being evaluated for cognitive impairment or dementia. Imaging with [18 F] florbetapir offers in vivo confirmation of the presence of cerebral amyloidosis and may increase the accuracy of the diagnosis and likely cause of cognitive impairment (CI) or dementia. Most importantly, amyloid imaging may improve certainty of etiology in situations where the differential diagnosis cannot be resolved on the basis of standard clinical and laboratory criteria. RESULTS: A consecutive case series of 30 patients (age 50-89; 16 M/14 F) were clinically evaluated at a cognitive evaluation center of urban dementia center and referred for [18 F] florbetapir PET imaging as part of a comprehensive dementia workup. Evaluation included neurological examination and neuropsychological assessment by dementia experts. [18 F] florbetapir PET scans were read by trained nuclear medicine physicians using the qualitative binary approach. Scans were rated as either positive or negative for the presence of cerebral amyloidosis. In addition to a comprehensive dementia evaluation, post [18 F] florbetapir PET imaging results caused diagnoses to be changed in 10 patients and clarified in 9 patients. Four patients presenting with SCI were negative for amyloidosis. These results show that [18 F] florbetapir PET imaging added diagnostic clarification and discrimination in over half of the patients evaluated. CONCLUSIONS: Amyloid imaging provided novel and essential data that: (1) caused diagnosis to be revised; and/or (2) prevented the initiation of incorrect or suboptimal treatment; and/or (3) avoided inappropriate referral to an anti-amyloid clinical trial.


Subject(s)
Alzheimer Disease/diagnostic imaging , Aniline Compounds , Decision Making , Ethylene Glycols , Quality of Life , Radiopharmaceuticals , Aged , Aged, 80 and over , Dementia/diagnostic imaging , Diagnosis, Differential , Female , Humans , Male , Middle Aged , Positron-Emission Tomography , Urban Population
3.
PLoS One ; 8(1): e54035, 2013.
Article in English | MEDLINE | ID: mdl-23326568

ABSTRACT

Although amnestic mild cognitive impairment (aMCI; often considered a prodromal phase of Alzheimer's disease, AD) is most recognized by its implications for decline in memory function, research suggests that deficits in attention are present early in aMCI and may be predictive of progression to AD. The present study used functional magnetic resonance imaging to examine differences in the brain during the attention network test between 8 individuals with aMCI and 8 neurologically healthy, demographically matched controls. While there were no significant behavioral differences between groups for the alerting and orienting functions, patients with aMCI showed more activity in neural regions typically associated with the networks subserving these functions (e.g., temporoparietal junction and posterior parietal regions, respectively). More importantly, there were both behavioral (i.e., greater conflict effect) and corresponding neural deficits in executive control (e.g., less activation in the prefrontal and anterior cingulate cortices). Although based on a small number of patients, our findings suggest that deficits of attention, especially the executive control of attention, may significantly contribute to the behavioral and cognitive deficits of aMCI.


Subject(s)
Alzheimer Disease/physiopathology , Attention/physiology , Brain Mapping , Cognitive Dysfunction/physiopathology , Aged , Aged, 80 and over , Alzheimer Disease/complications , Alzheimer Disease/diagnostic imaging , Amnesia/complications , Amnesia/diagnostic imaging , Amnesia/physiopathology , Brain/diagnostic imaging , Brain/physiopathology , Cognitive Dysfunction/complications , Cognitive Dysfunction/diagnostic imaging , Disease Progression , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neuropsychological Tests , Radiography
4.
Brain Res ; 1401: 18-29, 2011 Jul 15.
Article in English | MEDLINE | ID: mdl-21669408

ABSTRACT

The cingulate cortex frequently shows gray matter loss with age as well as gender differences in structure and function, but little is known about whether individual cingulate Brodmann areas show gender-specific patterns of age-related volume decline. This study examined age-related changes, gender differences, and the interaction of age and gender in the relative volume of cingulate gray matter in areas 25, 24, 31, 23, and 29, over seven decades of adulthood. Participants included healthy, age-matched men and women, aged 20-87 (n=70). Main findings were as follows: (1) The whole cingulate showed significant age-related volume declines (averaging 5.54% decline between decades, 20s-80s). Each of the five cingulate areas also showed a significant decline with age, and individual areas showed different patterns of decline across the decades: Smaller volume with age was most evident in area 31, followed by 25 and 24. (2) Women had relatively larger cingulate gray matter volume than men overall and in area 24. (3) Men and women showed different patterns of age-related volume decline in area 31, at midlife and late in life. By delineating normal gender differences and age-related morphometric changes in the cingulate cortex over seven decades of adulthood, this study improves the baseline for comparison with structural irregularities in the cingulate cortex associated with psychopathology. The Brodmann area-based approach also facilitates comparisons across studies that aim to draw inferences between age- and gender-related structural differences in the cingulate gyrus and corresponding differences in cingulate function.


Subject(s)
Aging/physiology , Gyrus Cinguli/anatomy & histology , Gyrus Cinguli/physiology , Sex Characteristics , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Organ Size , Young Adult
5.
Int J Neuropsychopharmacol ; 14(3): 389-98, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21029513

ABSTRACT

The Nicotrol® (Pfizer, USA) nicotine inhaler reduces craving by mimicking the behavioural component of cigarettes and delivering controlled doses of nicotine, which binds to the beta-2 subunit-containing nicotinic acetylcholine receptors (ß2*-nAChRs). Previous studies examined ß2*-nAChR occupancy after administration of regular and low-nicotine cigarettes. Here, we measured occupancy of ß2*-nAChRs after administration of nicotine via inhaler, and the relationship between occupancy and changes in craving for tobacco smoking and withdrawal symptoms. Tobacco smokers participated in [123I]5-IA-85380 SPECT studies with either a nicotine inhaler (n=9) or tobacco cigarette (n=4) challenge. [123I]5-IA was administered as a bolus plus constant infusion. After equilibrium was achieved, three 30-min baseline scans were collected, and subjects either used the nicotine inhaler or a regular cigarette, and up to six additional scans were obtained. Receptor occupancy was determined based on the Lassen plot method. Craving for tobacco smoking and withdrawal symptoms were evaluated pre- and post-challenge. Use of the nicotine inhaler produced an average 55.9±6.4% occupancy of ß2*-nAChRs 2-5 h post-challenge, whereas use of a cigarette produced significantly higher receptor occupancy (F=10.6, p=0.009) with an average 67.6±14.1% occupancy 1.5-5 h post-challenge. There was a significant decrease in withdrawal symptoms post-nicotine inhaler use (F=6.13, p=0.04). These results demonstrate significant differences in occupancy of ß2*-nAChRs by nicotine after use of the inhaler vs. a cigarette and confirm the ability of the nicotine inhaler to relieve withdrawal symptoms.


Subject(s)
Behavior, Addictive/drug therapy , Nicotine/pharmacology , Nicotinic Agonists/pharmacology , Receptors, Nicotinic/metabolism , Substance Withdrawal Syndrome/drug therapy , Administration, Inhalation , Adult , Female , Humans , Male , Middle Aged , Nicotine/administration & dosage , Nicotine/blood , Nicotinic Agonists/administration & dosage , Nicotinic Agonists/blood , Smoking , Smoking Cessation , Young Adult
6.
Behav Brain Res ; 218(2): 335-40, 2011 Apr 15.
Article in English | MEDLINE | ID: mdl-21115066

ABSTRACT

Schizotypal personality disorder (SPD) individuals and borderline personality disorder (BPD) individuals have been reported to show neuropsychological impairments and abnormalities in brain structure. However, relationships between neuropsychological function and brain structure in these groups are not well understood. This study compared visual-spatial working memory (SWM) and its associations with dorsolateral prefrontal cortex (DLPFC) and ventrolateral prefrontal cortex (VLPFC) gray matter volume in 18 unmedicated SPD patients with no BPD traits, 18 unmedicated BPD patients with no SPD traits, and 16 healthy controls (HC). Results showed impaired SWM in SPD but not BPD, compared with HC. Moreover, among the HC group, but not SPD patients, better SWM performance was associated with larger VLPFC (BA44/45) gray matter volume (Fisher's Z p-values <0.05). Findings suggest spatial working memory impairments may be a core neuropsychological deficit specific to SPD patients and highlight the role of VLPFC subcomponents in normal and dysfunctional memory performance.


Subject(s)
Memory, Short-Term/physiology , Prefrontal Cortex/physiopathology , Schizotypal Personality Disorder/physiopathology , Space Perception/physiology , Adult , Analysis of Variance , Borderline Personality Disorder/pathology , Borderline Personality Disorder/physiopathology , Brain Mapping , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neuropsychological Tests , Organ Size/physiology , Prefrontal Cortex/pathology , Schizotypal Personality Disorder/pathology , Severity of Illness Index
7.
Psychiatr Clin North Am ; 33(4): 757-81, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21093677

ABSTRACT

Traumatic brain injury (TBI) has been a major cause of mortality and morbidity in the wars in Iraq and Afghanistan. Blast exposure has been the most common cause of TBI, occurring through multiple mechanisms. What is less clear is whether the primary blast wave causes brain damage through mechanisms that are distinct from those common in civilian TBI and whether multiple exposures to low-level blast can lead to long-term sequelae. Complicating TBI in soldiers is the high prevalence of posttraumatic stress disorder. At present, the relationship is unclear. Resolution of these issues will affect both treatment strategies and strategies for the protection of troops in the field.


Subject(s)
Blast Injuries/complications , Brain Injuries/etiology , Military Personnel , Stress Disorders, Post-Traumatic/etiology , Warfare , Afghan Campaign 2001- , Blast Injuries/epidemiology , Brain Injuries/complications , Brain Injuries/epidemiology , Humans , Iraq War, 2003-2011 , Prevalence , Severity of Illness Index , Stress Disorders, Post-Traumatic/epidemiology
8.
Int J Geriatr Psychiatry ; 25(5): 531-9, 2010 May.
Article in English | MEDLINE | ID: mdl-19697298

ABSTRACT

OBJECTIVE: Longitudinal neuropsychological assessment provides the opportunity to observe the earliest transition to cognitive impairment in healthy, elderly individuals. We examined the feasibility, and its comparability to in-person assessment, of a telephone administered battery of established neuropsychological measures of cognitive functioning in healthy, elderly women. METHODS: Fifty-four women (age = 79 +/- 7.7; education = 15.4 +/- 3.3) who were in self-reported good health were recruited from senior centers and other community sources. A two-way cross-over design was used in which participants were randomly assigned to receive either (1) in-person neuropsychological assessment followed by telephone assessment and (2) telephone assessment followed by in-person assessment, separated by approximately 4 weeks. Linear regression models were used to determine whether there were performance differences by method (in-person vs. telephone), and equivalence testing assessed comparability of the two methods. RESULTS: There were no statistically significant differences in performance between in-person and telephone assessments on most neuropsychological tests, with the exception of digit span backward, Oral Trail Making Test Part A, and delayed recall on the SRT, the latter likely related to non-comparable exposure (6-trials in-person vs. 3-trials telephone). Equivalence testing differences fell in the pre-specified clinical equivalence zones, providing evidence of comparability of the two methods. CONCLUSIONS: These pilot data support telephone administration of a neuropsychological battery that yields comparable performance to in-person assessment with respect to most instruments. Significant differences in scores on some measures suggest care should be taken in selecting specific measures used in a neuropsychological battery administered by telephone.


Subject(s)
Cognition Disorders/diagnosis , Neuropsychological Tests , Telephone , Aged , Aged, 80 and over , Cross-Over Studies , Feasibility Studies , Female , Humans , Linear Models , Longitudinal Studies , Mass Screening/methods
9.
J Neurotrauma ; 27(1): 35-49, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19715400

ABSTRACT

In this study we investigated regional cerebral glucose metabolism abnormalities of [(18)F] fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging in traumatic brain injury (TBI). PET images of 81 TBI patients and 68 normal controls were acquired and a word list learning task was administered during the uptake period. The TBI group included 35 patients with positive structural imaging (CT or MRI) findings soon after injury, 40 patients with negative findings, and 6 cases without structural imaging. Statistical parametric mapping (SPM) analysis was applied with several levels of spatial smoothing. Cluster counting analysis was performed for each subject to identify abnormal clusters with contiguous voxel values that deviated by two standard deviations or more from the mean of the normal controls, and to count the number of clusters in 10 size categories. SPM maps demonstrated that the 81 patients had significantly lower FDG uptake than normal controls, widely across the cortex (including bilateral frontal and temporal regions), and in the thalamus. Cluster counting results indicated that TBI patients had a higher proportion of larger clusters than controls. These large low-FDG-uptake clusters of the TBI patients were closer to the brain edge than those of controls. These results suggest that deficits of cerebral metabolism in TBI are spread over multiple brain areas, that they are closer to the cortical surface than clusters in controls, and that group spatial patterns of abnormal cerebral metabolism may be similar in TBI patients with cognitive deficits with and without obvious acute abnormalities identified on structural imaging.


Subject(s)
Brain Injuries/diagnostic imaging , Brain Injuries/metabolism , Brain Mapping/methods , Brain/diagnostic imaging , Brain/metabolism , Image Processing, Computer-Assisted/methods , Positron-Emission Tomography/methods , Adult , Brain/physiopathology , Brain Injuries/physiopathology , Cerebral Hemorrhage, Traumatic/diagnostic imaging , Cerebral Hemorrhage, Traumatic/metabolism , Cerebral Hemorrhage, Traumatic/physiopathology , Cognition Disorders/diagnostic imaging , Cognition Disorders/metabolism , Cognition Disorders/physiopathology , Data Interpretation, Statistical , Diffuse Axonal Injury/diagnostic imaging , Diffuse Axonal Injury/metabolism , Diffuse Axonal Injury/physiopathology , Energy Metabolism/physiology , Female , Fluorodeoxyglucose F18 , Frontal Lobe/diagnostic imaging , Frontal Lobe/metabolism , Frontal Lobe/physiopathology , Humans , Male , Middle Aged , Temporal Lobe/diagnostic imaging , Temporal Lobe/metabolism , Temporal Lobe/physiopathology , Thalamus/diagnostic imaging , Thalamus/metabolism , Thalamus/physiopathology
10.
Neurobiol Aging ; 31(5): 826-38, 2010 May.
Article in English | MEDLINE | ID: mdl-19027195

ABSTRACT

This study examined the main and interactive effects of age and sex on relative glucose metabolic rate (rGMR) within gray matter of 39 cortical Brodmann areas (BAs) and the cingulate gyrus using (18)FDG-PET during a verbal memory task in 70 healthy normal adults, aged 20-87 years. Women showed significantly greater age-related rGMR decline in left cingulate gyrus than men (BAs 25, 24, 23, 31, 29). Both groups showed a decline in the anterior cingulate--a neuroanatomical structure that mediates effective cognitive-emotional interactions (BAs 32, 24, 25), while the other frontal regions did not show substantial decline. No sex differences in rGMR were identified within temporal, parietal and occipital lobes. Sex differences were observed for rGMR within subcomponents of the cingulate gyrus with men higher in BA25 and BA29, but lower in BA24 and BA 23 compared to women. For men, better memory performance was associated with greater rGMR in BA24, whereas in women better performance was associated with orbitofrontal-BA12. These results suggest that both age-related metabolic decline and sex differences within frontal regions are more marked in medial frontal and cingulate areas, consistent with some age-related patterns of affective and cognitive change.


Subject(s)
Aging/physiology , Brain/physiology , Mental Recall/physiology , Serial Learning/physiology , Adult , Age Factors , Aged , Aged, 80 and over , Analysis of Variance , Brain/diagnostic imaging , Brain Mapping , Female , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Middle Aged , Neuropsychological Tests , Radionuclide Imaging , Sex Factors , Verbal Behavior/physiology
11.
J Nucl Med ; 50(9): 1455-63, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19690024

ABSTRACT

UNLABELLED: Postmortem binding studies have established that the concentration of alpha(4)beta(2)-nicotinic acetylcholine receptors (alpha(4)beta(2)-nAChR) is reduced in advanced Alzheimer disease (AD). However, the status of this receptor in mild or prodromal AD has remained the subject of controversy. METHODS: We compared alpha(4)beta(2)-nAChR availability in 8 brain regions of living human subjects who had AD and mild cognitive impairment (MCI) with that in age-matched healthy control subjects by using the ligand (123)I-5-IA-85380 ((123)I-5-IA) and SPECT. All subjects (n = 32) were nonsmokers; they were administered (123)I-5-IA as a bolus plus a constant infusion and imaged 6-8 h later under equilibrium conditions. The effect of diagnosis on regional alpha(4)beta(2)-nAChR availability (regional brain activity/total parent concentration in plasma, proportional to the binding potential) was analyzed using multivariate analysis of covariance, controlling for the effects of age and sex. RESULTS: Despite a significant overall effect of diagnostic group on mean alpha(4)beta(2)-nAChR availability, univariate analyses revealed no group differences for any brain region analyzed. An exploratory analysis of the relationship between regional alpha(4)beta(2)-nAChR availability and neuropsychologic variables yielded several plausible correlations. However, after Bonferroni adjustment, only the correlation between the anterior cingulate and the Trail Making Test, Part B, in the healthy control subjects remained significant. CONCLUSION: These results are consistent with several postmortem and in vivo studies suggesting the preservation of nAChRs during the prodromal and early stages of AD. They support the interpretation that nAChR and other cholinergic reductions in AD are late-stage phenomena.


Subject(s)
Alzheimer Disease/metabolism , Azetidines/pharmacokinetics , Brain/metabolism , Cognition Disorders/metabolism , Pyridines/pharmacokinetics , Receptors, Nicotinic/metabolism , Tomography, Emission-Computed, Single-Photon/methods , Aged , Alzheimer Disease/complications , Alzheimer Disease/diagnostic imaging , Brain/diagnostic imaging , Cognition Disorders/complications , Cognition Disorders/diagnostic imaging , Feasibility Studies , Female , Humans , Male , Radiopharmaceuticals/pharmacokinetics , Reproducibility of Results , Sensitivity and Specificity , Tissue Distribution
12.
Psychiatry Res ; 173(3): 212-7, 2009 Sep 30.
Article in English | MEDLINE | ID: mdl-19682865

ABSTRACT

Postmortem studies show reductions in brain serotonin 2A (5-HT(2A)) receptors in Alzheimer's disease (AD). Converging evidence also suggests that serotonergic dysregulation may contribute to behavioral symptoms that frequently occur in AD. This study aimed to define regional reductions in 5-HT(2A) binding in AD patients and to examine their behavioral correlates. Nine patients with probable AD and eight elderly controls were studied using a constant infusion paradigm for equilibrium modeling of [(18)F]deuteroaltanserin with positron emission tomography (PET). Region of interest analyses were performed on PET images coregistered to MRI scans. The outcome measures BP(P) (ratio of specific brain uptake to total plasma parent concentration) and BP(ND) (ratio of specific to nondisplaceable uptake) were obtained for pertinent cortical and subcortical regions. AD patients showed a statistically significant decrease in the anterior cingulate in both BP(P) and BP(ND), but in no other region. Within the AD patient sample, no significant correlations were observed between regional 5-HT(2A) binding and behavioral measures, including depressive and psychotic symptoms. These results confirm a reduction in cortical 5-HT(2A) receptors in AD, specifically in the anterior cingulate. However, in a limited AD patient sample, they fail to demonstrate a relationship between regional 5-HT(2A) binding and major behavioral symptoms.


Subject(s)
Alzheimer Disease , Brain Mapping , Brain/metabolism , Positron-Emission Tomography/methods , Receptor, Serotonin, 5-HT2A/metabolism , Aged , Aged, 80 and over , Alzheimer Disease/diagnostic imaging , Alzheimer Disease/pathology , Alzheimer Disease/physiopathology , Analysis of Variance , Brain/diagnostic imaging , Brain/drug effects , Brief Psychiatric Rating Scale , Female , Fluorine Radioisotopes/metabolism , Humans , Ketanserin/analogs & derivatives , Ketanserin/metabolism , Male , Middle Aged , Protein Binding/physiology
13.
Neurobiol Aging ; 30(9): 1490-7, 2009 Sep.
Article in English | MEDLINE | ID: mdl-18242781

ABSTRACT

Human postmortem studies have reported decreases with age in high affinity nicotine binding in brain. We investigated the effect of age on beta(2)-containing nicotinic acetylcholine receptor (beta(2)-nAChR) availability in eight brain regions of living human subjects using the ligand [(123)I]5-IA-85380 ([(123)I]5-IA) and single photon emission computed tomography (SPECT). Healthy, nonsmokers (N=47) ranging in age from 18 to 85 were administered [(123)I]5-IA using a bolus plus constant infusion paradigm and imaged 6-8h later under equilibrium conditions. The effect of age on regional beta(2)-nAChR availability (V(T), regional brain activity/free plasma parent, a measure proportional to the binding potential) was analyzed using linear regression and Pearson's correlation (r). Age and regional beta(2)-nAChR availability were inversely correlated in seven of the eight brain regions analyzed, with decline ranging from 32% (thalamus) to 18% (occipital cortex) over the adult lifespan, or up to 5% per decade. These results in living human subjects corroborate postmortem reports of decline in high affinity nicotine binding with age and may aid in elucidating the role of beta(2)-nAChRs in cognitive aging.


Subject(s)
Aging/metabolism , Brain Chemistry/physiology , Brain/metabolism , Cognition Disorders/metabolism , Down-Regulation/physiology , Receptors, Nicotinic/metabolism , Adolescent , Adult , Aged , Aged, 80 and over , Azetidines , Brain/anatomy & histology , Brain/physiopathology , Cognition Disorders/diagnostic imaging , Cognition Disorders/physiopathology , Female , Humans , Iodine Radioisotopes , Linear Models , Male , Middle Aged , Pyridines , Receptors, Nicotinic/analysis , Tomography, Emission-Computed, Single-Photon/methods , Young Adult
14.
J Nucl Med ; 48(10): 1633-40, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17873128

ABSTRACT

UNLABELLED: The study of the effects of sex and hormones on brain chemistry and neurotransmission is of increasing importance as evidence emerges of sex differences in behavioral symptoms and treatment response in neuropsychiatric disorders. The nicotinic acetylcholine receptor (nAChR) system has been implicated in a variety of psychiatric disorders, including tobacco smoking, for which there is strong evidence supporting sex differences in behaviors and response to smoking cessation treatments. We examined the availability of nAChR containing the beta(2) subunit in healthy men and women and the influence of menstrual phase among women. METHODS: Ten men and 19 women nonsmokers underwent one (123)I-5-IA-85380 ((123)I-5-IA) SPECT scan and one MRI scan. A subset of 9 women, aged 18-39 y, underwent a second (123)I-5-IA scan. These 9 women were scanned during the early follicular (days 4-7 in 8 subjects and day 11 in 1 subject) and mid-luteal (days 19-25) phases of their menstrual cycle. Hormone levels were measured in all women to confirm the phase of the cycle. RESULTS: Regional brain activity (kBq/cm(3)) was higher (39%-54%) in women than in men nonsmokers. When regional brain activity was normalized to total plasma parent to correct for individual differences in radiotracer metabolism (V(T)'), differences of 10%-16% were observed, with women greater than men. In contrast, when regional brain activity was normalized to free plasma parent (V(T)), there was less than a 4% difference by sex in regional brain beta(2)-nAChR availability. These sex differences in kBq/cm(3) and V(T)' resulted from significantly higher levels of total plasma parent, free fraction (f(1)), and free plasma parent in women than in men nonsmokers. No differences in plasma measures or brain beta(2)-nAChR availability were observed across the menstrual cycle for any outcome measure. CONCLUSION: Overall, these findings demonstrate no significant difference in brain beta(2)-nAChR availability between men and women nonsmokers or across the menstrual cycle. Importantly, these findings demonstrate sex differences in radiotracer metabolism and plasma protein binding and highlight the critical need to measure plasma radiotracer levels and f(1) in studies that include both sexes.


Subject(s)
Azetidines/pharmacokinetics , Brain/metabolism , Menstrual Cycle/metabolism , Pyridines/pharmacokinetics , Receptors, Nicotinic/metabolism , Smoking/metabolism , Adult , Brain/diagnostic imaging , Female , Humans , Male , Radiopharmaceuticals/pharmacokinetics , Sex Factors , Tissue Distribution , Tomography, Emission-Computed, Single-Photon
15.
Ann N Y Acad Sci ; 1097: 168-70, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17413019

ABSTRACT

Human postmortem studies have reported decreases with age in high-affinity nicotine binding in brain. We have been investigating in vivo the availability of the beta(2)-containing nicotinic acetylcholine receptor (beta(2)-nAChR) in healthy nonsmokers (18-85 years of age) using [(123)I]5-IA-85380 SPECT imaging. Age and regional beta(2)-nAChR availability (V(T)(,)) have been observed to be inversely correlated in all brain regions analyzed, with decline ranging from 21% (cerebellum) to 36% (thalamus), or by up to 5% per decade of life. Preliminary results have confirmed postmortem reports of age-related decline in high-affinity nicotine binding with age and may elucidate the role of beta(2)-nAChRs in the cognitive decline associated with aging.


Subject(s)
Azetidines , Brain Chemistry/physiology , Brain/diagnostic imaging , Pyridines , Radiopharmaceuticals , Receptors, Nicotinic/drug effects , Adolescent , Adult , Aged , Aged, 80 and over , Aging/physiology , Brain/growth & development , Cerebellum/growth & development , Cerebellum/pathology , Female , Humans , Male , Middle Aged , Thalamus/growth & development , Thalamus/pathology , Tomography, Emission-Computed, Single-Photon
16.
J Clin Exp Neuropsychol ; 26(3): 393-404, 2004 May.
Article in English | MEDLINE | ID: mdl-15512928

ABSTRACT

Barkley's hybrid model of executive functions (EFs) predicts that individuals with deficient inhibitory control should show impairment of EFs. Thirty-eight nonreferred young adults were administered tests of EFs and four laboratory measures of inhibitory control: Stop Signal (SS), Go No-Go, Competing Motor Program (CMP), and Stroop Color-Word tests. Behavioral ratings of impulsivity were collected using the Barratt Impulsivity Scale-11 (BIS-11). CMP and SS accounted for a significant proportion of variance in measures of EFs beyond that accounted for by IQ. Additionally, increased impulsivity, as measured by the BIS-11, was associated with poorer performance on some tests of EFs. These findings provide partial support for Barkley's theory in that effective executive functioning is associated with sufficient inhibitory control.


Subject(s)
Inhibition, Psychological , Problem Solving/physiology , Adolescent , Adult , Female , Humans , Intelligence/physiology , Male , Models, Psychological , Neuropsychological Tests/statistics & numerical data , Psychometrics/methods , Psychomotor Performance/physiology , Reaction Time/physiology
SELECTION OF CITATIONS
SEARCH DETAIL
...