Jason Brandt

Dr. Jason Brandt

Johns Hopkins University School of Medicine
orcid

Research Focus & Metrics

Academic Career Length

48Years (1979-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 1998 in The Clinical Neuropsychologist
Verified
Journal Article
Closed access
RBRalph H.B. Benedict
Ralph H.B. Benedict
DSDavid Schretlen
David Schretlen
LGLowell Groninger
Lowell Groninger
Jason BrandtJason Brandt
Jason Brandt

1 April 1991 in The Clinical Neuropsychologist
Verified
Journal Article
Closed access
Jason BrandtJason Brandt
Jason Brandt
A new test of verbal learning and memory, the Hopkins Verbal Learning Test, was developed. The test consists of three trials of free-recall of a 12-item, semantically categorized list, followed by yes/no recognition. Six parallel forms yielded equivalent results in normals. The performance of patients with Alzheimer's disease and chronic amnesia is described. The test is likely to be useful in patients too impaired for more comprehensive memory assessments and where repeated testing is necessary.

1 October 1996 in The Lancet
Verified
Journal Article
Open access
ABAnn B Bruner
Ann B Bruner
AJAlain Joffe
Alain Joffe
ADAnne K Duggan
Anne K Duggan
JCJames F Casella
James F Casella
Jason BrandtJason Brandt
Jason Brandt
Up to 25% of adolescent girls in the USA are iron deficient. This double-blind, placebo-controlled clinical trial assessed the effects of iron supplementation on cognitive function in adolescent girls with non-anaemic iron deficiency. 716 girls who enrolled at four Baltimore high schools were screened for non-anaemic iron deficiency (serum ferritin < or = 12 micrograms/L with normal haemoglobin). 98 (13.7%) girls had non-anaemic iron deficiency of whom 81 were enrolled in the trial. Participants were randomly assigned oral ferrous sulphate (650 mg twice daily) or placebo for 8 weeks. The effect of iron treatment was assessed by questionnaires and haematological and cognitive tests, which were done before treatment started and repeated after the intervention. We used four tests of attention and memory to measure cognitive functioning. Intention-to-treat and per-protocol analyses were done. Of the 81 enrolled girls with non-anaemic iron deficiency, 78 (96%) completed the study (39 in each group). Five girls (three control, two treatment) developed anaemia during the intervention and were excluded from the analyses. Thus, 73 girls were included in the per-protocol analysis. Ethnic distribution, mean age, serum ferritin concentrations, haemoglobin concentrations, and cognitive test scores of the groups did not differ significantly at baseline. Postintervention haematological measures of iron status were significantly improved in the treatment group (serum ferritin 27.3 vs 12.1 micrograms/L, p < 0.001). Regression analysis showed that girls who received iron performed better on a test of verbal learning and memory than girls in the control group (p < 0.02). In this urban population of non-anaemic iron-deficient adolescent girls, iron supplementation improved verbal learning and memory.

9 August 1999 in The Clinical Neuropsychologist
Verified
Journal Article
Closed access
ASAnne M. Shapiro
Anne M. Shapiro
RBRalph H.B. Benedict
Ralph H.B. Benedict
DSDavid Schretlen
David Schretlen
Jason BrandtJason Brandt
Jason Brandt
The present investigation examined the validity of the revised Hopkins Verbal Learning Test (HVLT-R). In a principal components analysis with varimax rotation, measures of new learning and delayed ...

13 July 2004 in Neurology
Verified
Journal Article
Closed access
PDF file
EAE. H. Aylward
E. H. Aylward
BSB. F. Sparks
B. F. Sparks
KFK. M. Field
K. M. Field
VYV. Yallapragada
V. Yallapragada
BSB. D. Shpritz
B. D. Shpritz
CRC. A. Ross
C. A. Ross
Background: Huntington disease (HD) is characterized by striatal atrophy that begins long before the onset of motor symptoms. Objective: To determine when striatal atrophy begins, the extent and rate of atrophy before diagnosis of motor symptoms, and whether striatal atrophy can predict when symptom onset will occur. Methods: Caudate and putamen volumes were measured on MRI scans of 19 preclinical subjects with the HD gene expansion who were very far (9 to 20 years) from estimated onset, and on serial scans from 17 preclinical subjects, six of whom were diagnosed with HD within 5 years after the initial scan. Results: Striatal volumes were significantly smaller for the subjects who were very far from estimated onset than for age-matched control subjects. Statistical models fit to the longitudinal data suggest that rate of caudate atrophy becomes significant when subjects are approximately 11 years from estimated onset and rate of putamen atrophy becomes significant approximately 9 years prior to onset. In the six incident cases, caudate and putamen were approximately one-third to one-half of normal volume at diagnosis, and caudate volume alone was able to predict with 100% accuracy those subjects who would be diagnosed within 2 years of imaging. Conclusions: Striatal atrophy begins many years prior to diagnosable HD, and assessment of atrophy on MRI may be very useful in both predicting HD onset and in tracking progression in future therapeutic trials in preclinical subjects.

1 July 2003 in Archives of General Psychiatry
Verified
Journal Article
Open access
PDF file
CLConstantine Lyketsos
Constantine Lyketsos
LDLourdes DelCampo
Lourdes DelCampo
MSMartin H Steinberg
Martin H Steinberg
QMQuincy Miles
Quincy Miles
CSCynthia D. Steele
Cynthia D. Steele
PRPeter V. Rabins
Peter V. Rabins
ALZHEIMER DISEASE (AD) is a progressive disease with debilitating consequences for patients, their families, and the public welfare. While cognitive and functional decline is the hallmark of AD, neuropsychiatric disturbances afflict about 90% of the patients.1-8 The treatment of neuropsychiatric disturbances is an essential part of the treatment of AD.2,9,10 Despite this, the evidence supporting the use of interventions for these disturbances has been sparse.10