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1.
J Dent Educ ; 83(2 Suppl): S23-S27, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30709936

ABSTRACT

Access to quality dental care for many adults and children remains a serious concern. Many communities throughout the U.S. are at great disadvantage for preventive care and treatment due to payment concerns, location and types of providers, and poor communication between dental providers and primary care professionals. Voids in shared technology and information also persist. Integrating primary care with oral health can boost both preventive care and interventions focused on increasing efficacy and efficiency between dental and primary care professionals in addressing the onset and duration of disease. Academic and community partnerships can help increase access to care and bring together the dental and medical communities for better integration and care coordination. Academic and community partnerships promote the sharing of information, facilitate provision of basic diagnostic services, and bring the bidirectional flow of knowledge, training, and skills to one another in a systematic and sustained manner.


Subject(s)
Cooperative Behavior , Dental Care , Health Services Accessibility/organization & administration , Education, Dental , United States
2.
Nano Lett ; 17(12): 7306-7314, 2017 12 13.
Article in English | MEDLINE | ID: mdl-29136386

ABSTRACT

Chemical vapor deposition (CVD) has been established as the most effective way to grow large area two-dimensional materials. Direct study of the etching process can reveal subtleties of this competing with the growth reaction and thus provide the necessary details of the overall growth mechanism. Here we investigate hydrogen-induced etching of hBN and graphene and compare the results with the classical kinetic Wulff construction model. Formation of the anisotropically etched holes in the center of hBN and graphene single crystals was observed along with the changes in the crystals' circumference. We show that the edges of triangular holes in hBN crystals formed at regular etching conditions are parallel to B-terminated zigzags, opposite to the N-terminated zigzag edges of hBN triangular crystals. The morphology of the etched hBN holes is affected by a disbalance of the B/N ratio upon etching and can be shifted toward the anticipated from the Wulff model N-terminated zigzag by etching in a nitrogen buffer gas instead of a typical argon. For graphene, etched hexagonal holes are terminated by zigzag, while the crystal circumference is gradually changing from a pure zigzag to a slanted angle resulting in dodecagons.

3.
PLoS One ; 10(3): e0119718, 2015.
Article in English | MEDLINE | ID: mdl-25803307

ABSTRACT

We have previously shown that Annexin A8 (ANXA8) is strongly associated with the basal-like subgroup of breast cancers, including BRCA1-associated breast cancers, and poor prognosis; while in the mouse mammary gland AnxA8 mRNA is expressed in low-proliferative isolated pubertal mouse mammary ductal epithelium and after enforced involution, but not in isolated highly proliferative terminal end buds (TEB) or during pregnancy. To better understand ANXA8's association with this breast cancer subgroup we established ANXA8's cellular distribution in the mammary gland and ANXA8's effect on cell proliferation. We show that ANXA8 expression in the mouse mammary gland was strong during pre-puberty before the expansion of the rudimentary ductal network and was limited to a distinct subpopulation of ductal luminal epithelial cells but was not detected in TEB or in alveoli during pregnancy. Similarly, during late involution its expression was found in the surviving ductal epithelium, but not in the apoptotic alveoli. Double-immunofluorescence (IF) showed that ANXA8 positive (+ve) cells were ER-alpha negative (-ve) and mostly quiescent, as defined by lack of Ki67 expression during puberty and mid-pregnancy, but not terminally differentiated with ∼15% of ANXA8 +ve cells re-entering the cell cycle at the start of pregnancy (day 4.5). RT-PCR on RNA from FACS-sorted cells and double-IF showed that ANXA8+ve cells were a subpopulation of c-kit +ve luminal progenitor cells, which have recently been identified as the cells of origin of basal-like breast cancers. Over expression of ANXA8 in the mammary epithelial cell line Kim-2 led to a G0/G1 arrest and suppressed Ki67 expression, indicating cell cycle exit. Our data therefore identify ANXA8 as a potential mediator of quiescence in the normal mouse mammary ductal epithelium, while its expression in basal-like breast cancers may be linked to ANXA8's association with their specific cells of origin.


Subject(s)
Annexins/metabolism , Cell Cycle Checkpoints/physiology , Endothelial Progenitor Cells/metabolism , Gene Expression Regulation, Developmental/physiology , Mammary Glands, Animal/metabolism , Age Factors , Animals , Blotting, Western , Bromodeoxyuridine , Colony-Forming Units Assay , Female , Flow Cytometry , Fluorescent Antibody Technique , Immunohistochemistry , Ki-67 Antigen/metabolism , Mammary Glands, Animal/cytology , Mammary Glands, Animal/growth & development , Mice , Pregnancy , Proto-Oncogene Proteins c-kit/metabolism , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction
4.
J Healthc Qual ; 34(2): 12-20, 2012.
Article in English | MEDLINE | ID: mdl-23552199

ABSTRACT

UNLABELLED: Most healthcare quality improvement and cost reduction efforts currently focus on care processes, or transitions-for example, the hospital discharge process. While identification and adoption of best practices to address these aspects of healthcare are essential, more is needed for systems that serve vulnerable populations: to account for social factors that often inhibit patients' ability to take full advantage of available healthcare. Our urban safety net healthcare system developed and implemented an innovative quality improvement approach. The programs, Guided Chronic Care(TM) , and Passport to Wellness, use Assertive Care and provide social support for patients between medical encounters, enabling patients to make better use of the healthcare system and empowering them to better manage their conditions. RESULTS: The majority of patients reported problems with mobility and nearly half reported anxiety or depression. Early indications show improved quality of care and significant reduction in costs. Challenges encountered and lessons learned in implementing the programs are described, to assist others developing similar interventions.


Subject(s)
Chronic Disease/therapy , Quality of Health Care , Safety-net Providers/organization & administration , Vulnerable Populations , Chronic Disease/economics , Chronic Disease/psychology , Cost Control/methods , Female , Humans , Male , Middle Aged , Qualitative Research , Safety-net Providers/standards , Social Support , Socioeconomic Factors , Urban Health
5.
ACS Nano ; 4(3): 1377-84, 2010 Mar 23.
Article in English | MEDLINE | ID: mdl-20201542

ABSTRACT

In this report, we present a description of the optical and electronic properties of as-deposited, annealed, and chemically treated single-walled carbon nanotube (SWNT) films showing metallic or semiconducting behavior. As-deposited and annealed semiconducting SWNT films were significantly less conductive than metallic SWNT films; however, chemical treatment of semiconducting SWNT films resulted in sheet resistance values as low as 60 Omega x sq(-1) in comparison to 76 Omega x sq(-1) for similarly processed metallic SWNT films. We conclude that the greater improvement of electrical conductivity observed in the semiconducting SWNT film results from the difference in the density of available electronic states between metallic and semiconducting SWNTs. A corroborative investigation of the change in surface work function and the chemical composition of SWNT films, as revealed by X-ray photoelectron spectroscopy, is provided to support these conclusions and to give new perspective to the formation of electronically homogeneous SWNT networks.

6.
J Clin Sleep Med ; 5(1): 21-7, 2009 Feb 15.
Article in English | MEDLINE | ID: mdl-19317377

ABSTRACT

STUDY OBJECTIVES: Obstructive sleep apnea (OSA) is associated with cognitive impairments in working memory (WM). Neuronal activation during WM tasks can be indirectly assessed by blood oxygen level-dependent functional magnetic resonance imaging (BOLD-fMRI). The purpose of this study was to describe BOLD-fMRI responses during 2 separate working memory tasks and a finger tapping task in men with OSA. A secondary aim was to explore the possible relation between OSA severity (apnea/hypopnea index) and BOLD-fMRI signal patterns. METHODS: Nine treatment-naïve men (mean age [+/- SD] of 45.7 [+/- 6.6] years) with OSA underwent BOLD fMRI testing on a research-dedicated university-based MRI scanner. During BOLD-fMRI subjects performed a Paced Auditory Serial Addition task (PASAT), an auditory N-Back task (2-BACK) task, and an alternating finger tapping. RESULTS: PASAT and 2-BACK tasks produced similar patterns of increased bilateral activation in posterior parietal, prefrontal and cerebellar regions. BOLD signal deactivations were observed within posterior cingulate, retrosplenial and inferior frontal regions during PASAT and 2-BACK, but not during tapping. With increased disease severity, BOLD activation patterns were increased in the right parietal lobe, but decreased in the cerebellar vermis. CONCLUSIONS: These preliminary findings suggest that the severity of OSA may correlate with neural activation during tasks of working memory, potentially reflecting compensatory neural responses in severe disease.


Subject(s)
Brain/physiopathology , Magnetic Resonance Imaging , Memory, Short-Term/physiology , Oxygen/blood , Sleep Apnea, Obstructive/physiopathology , Synaptic Transmission/physiology , Adult , Arousal/physiology , Attention/physiology , Cerebellum/physiopathology , Dominance, Cerebral/physiology , Frontal Lobe/physiopathology , Gyrus Cinguli/physiopathology , Humans , Male , Middle Aged , Motor Activity/physiology , Neuropsychological Tests , Parietal Lobe/physiopathology , Polysomnography , Prefrontal Cortex/physiopathology , Problem Solving/physiology , Serial Learning/physiology , Sleep Apnea, Obstructive/diagnosis
7.
Milbank Q ; 86(2): 241-72, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18522613

ABSTRACT

CONTEXT: Racial and ethnic disparities in health care in the United States have been well documented, with research largely focusing on describing the problem rather than identifying the best practices or proven strategies to address it. METHODS: In 2006, the Disparities Solutions Center convened a one-and-a-half-day Strategy Forum composed of twenty experts from the fields of racial/ethnic disparities in health care, quality improvement, implementation research, and organizational excellence, with the goal of deciding on innovative action items and adoption strategies to address disparities. The forum used the Results Based Facilitation model, and several key recommendations emerged. FINDINGS: The forum's participants concluded that to identify and effectively address racial/ethnic disparities in health care, health care organizations should: (1) collect race and ethnicity data on patients or enrollees in a routine and standardized fashion; (2) implement tools to measure and monitor for disparities in care; (3) develop quality improvement strategies to address disparities; (4) secure the support of leadership; (5) use incentives to address disparities; and (6) create a message and communication strategy for these efforts. This article also discusses these recommendations in the context of both current efforts to address racial and ethnic disparities in health care and barriers to progress. CONCLUSIONS: The Strategy Forum's participants concluded that health care organizations needed a multifaceted plan of action to address racial and ethnic disparities in health care. Although the ideas offered are not necessarily new, the discussion of their practical development and implementation should make them more useful.


Subject(s)
Communication Barriers , Ethnicity , Health Care Reform/organization & administration , Healthcare Disparities/classification , Quality of Health Care/organization & administration , Data Collection/methods , Healthcare Disparities/statistics & numerical data , Humans , National Academies of Science, Engineering, and Medicine, U.S., Health and Medicine Division , Quality of Health Care/statistics & numerical data , United States
8.
Neuropsychology ; 21(4): 507-13, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17605583

ABSTRACT

Variable reports of neuropsychological deficits in individuals with chronic fatigue syndrome (CFS) may, in part, be attributable to methodological limitations. In this study, these limitations were addressed by controlling for genetic and environmental influences and by assessing the effects of comorbid depression and mode of illness onset. Specifically, the researchers conducted a co-twin control study of 22 pairs of monozygotic twins, in which 1 twin met strict criteria for CFS and the co-twin was healthy. Twins underwent a structured psychiatric interview and comprehensive neuropsychological assessment evaluating 6 cognitive domains. Results indicated that twin groups had similar intellectual and visual memory functioning, but fatigued twins exhibited decreases in motor functions (p = .05), speed of information processing (p = .02), verbal memory (p = .02), and executive functioning (p = .01). Major depression did not affect neuropsychological functioning among fatigued twins, although twins with sudden illness onset demonstrated slowed information processing compared with those with gradual onset (p = .01). Sudden onset CFS was associated with reduced speed of information processing. If confirmed, these findings suggest the need to distinguish illness onset in future CFS studies and may have implications for treatment, cognitive rehabilitation, and disability determination.


Subject(s)
Cognition/physiology , Fatigue Syndrome, Chronic/psychology , Mental Processes/physiology , Adult , Attention/physiology , Depressive Disorder, Major/complications , Depressive Disorder, Major/psychology , Female , Humans , Male , Memory/physiology , Middle Aged , Neuropsychological Tests , Psychiatric Status Rating Scales , Psychomotor Performance/physiology , Reaction Time/physiology , Recognition, Psychology/physiology , Twins, Monozygotic , Verbal Learning/physiology , Wechsler Scales
9.
J Public Health Manag Pract ; 13(1): 23-30, 2007.
Article in English | MEDLINE | ID: mdl-17149096

ABSTRACT

The Strategic National Stockpile (SNS) is a national repository of pharmaceuticals and other medical supplies forseeably needed during a medical disaster. In the event of SNS deployment, state and local public health authorities must be prepared to receive, distribute, and dispense the materials. We propose a cache of supplies, termed the "POD go-kit," prepared in advance and locally available prior to the establishment of Points of Dispensing (POD) for SNS material. Characteristics of the preassembled go-kit are its multiplicity of use, ease of storage and transportation, minimal redundancy with SNS material, and packaging in a manner consistent with POD function. The POD go-kit is assembled into 4 separate "subkits": administrative supplies, patient routing supplies, dispensing supplies, and POD staff protection supplies. Incorporating existing practices from the SNS Listserv, this article itemizes the contents of the POD go-kit and its subkits and provides a rationale for its packaging. The Division of Strategic National Stockpile (DSNS) has not certified the proposed "POD go-kit" as a standardized POD go-kit.


Subject(s)
Disasters , Models, Organizational , Pharmaceutical Preparations/supply & distribution , Humans , United States
10.
Clin Neuropsychol ; 20(2): 271-88, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16690547

ABSTRACT

The Trail Making Test (TMT) frequently is used as a measure of executive cognitive function. However, traditional use of test completion time as the primary outcome score does not give the more detailed information on cognitive processes that analysis of test-taking errors may provide. The present study compared TMT performance of three groups: patients with schizophrenia, patients with major depression, and healthy control participants (n = 30 for each group). Three operationally defined error types were examined: (a) tracking, (b) perseverative, and (c) proximity. Although both patient groups were slower than the healthy control group, only the schizophrenia group made significantly more errors, particularly tracking errors, suggesting a greater degree of cognitive disorganization. Within-group analysis of a larger group of schizophrenia patients (n = 84) revealed that TMT time was most strongly associated with the Withdrawal-Retardation factor of the Brief Psychiatric Rating scale. In contrast, TMT errors were most strongly associated with the Conceptual Disorganization factor. Comparisons of TMT scores and other cognitive tests showed moderate to high associations with tests of working memory, psychomotor speed, and executive function. Stepwise regression analysis revealed an independent association between Digit Cancellation and Part B Time, indicating a unique contribution of visuomotor scanning to performance. In contrast, Part B errors were uniquely associated with the Verbal Series Attention Test and the Token Test, tests of mental tracking and executive-mediated working memory, respectively. These findings demonstrate the utility of TMT error analysis in revealing cognitive deficits not traditionally captured using completion time as the sole outcome variable.


Subject(s)
Cognition/physiology , Depression/diagnosis , Problem Solving/physiology , Schizophrenia/diagnosis , Trail Making Test/standards , Adult , Case-Control Studies , Depression/physiopathology , Diagnosis, Differential , Female , Humans , Male , Multivariate Analysis , Regression Analysis , Schizophrenia/physiopathology , Time Factors , Trail Making Test/statistics & numerical data
11.
J Cell Physiol ; 206(1): 16-24, 2006 Jan.
Article in English | MEDLINE | ID: mdl-15920758

ABSTRACT

Mammary morphogenesis in the mouse is driven by specialized structures at the ends of the developing ducts, the terminal end buds (TEB). The mechanisms controlling the precise branching and spacing of the ducts are, as yet, unknown. To identify genes that are associated with migration of TEB and differentiation of the subtending ducts, we developed a novel method of isolating TEB and ducts free of stroma, and compared the gene expression profiles of these two isolates using oligonucleotide microarrays. Ninety one genes were upregulated in TEB compared to ducts. Three of these genes, Sprr1A, Sema3B, and BASP1, are associated with axonal growth and guidance. Two additional members of the Sprr family, Sprr2A and 2B, not previously associated with axonal growth, were also highly expressed in TEB. Expression of these genes was confirmed by RT-PCR and Western blotting, and the cellular distribution of Sprr1A and BASP1 was demonstrated by immunohistochemistry. Other semaphorins, including Sema3C, 4A, 4F and the cancer invasion associated Sema 4D were also expressed in the mouse mammary gland along with the semaphorin receptors, Plexins A2, A3, B2, and D1, and Neuropilins 1 and 2. These results are discussed in the context of other proteins expressed in the developing gland that are known to be downstream effectors of these signaling molecules. We suggest that these genes may influence ductal growth and morphogenesis in the developing mammary gland.


Subject(s)
Axons/metabolism , Mammary Glands, Animal , Morphogenesis , Signal Transduction/physiology , Animals , Calmodulin-Binding Proteins/genetics , Calmodulin-Binding Proteins/metabolism , Cell Adhesion Molecules/genetics , Cell Adhesion Molecules/metabolism , Cell Movement/physiology , Cornified Envelope Proline-Rich Proteins , Cytoskeletal Proteins/genetics , Cytoskeletal Proteins/metabolism , Female , Gene Expression Profiling , Gene Expression Regulation, Developmental , In Vitro Techniques , Mammary Glands, Animal/anatomy & histology , Mammary Glands, Animal/growth & development , Mammary Glands, Animal/physiology , Membrane Proteins/genetics , Membrane Proteins/metabolism , Mice , Mice, Inbred BALB C , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Neuropilins/genetics , Neuropilins/metabolism , Oligonucleotide Array Sequence Analysis , Pregnancy , Protein Isoforms/genetics , Protein Isoforms/metabolism , Semaphorins/genetics , Semaphorins/metabolism
12.
Clin Cancer Res ; 11(19 Pt 1): 6872-9, 2005 Oct 01.
Article in English | MEDLINE | ID: mdl-16203777

ABSTRACT

PURPOSE: Microarray studies have linked Annexin A8 RNA expression to a "basal cell-like" subset of breast cancers, including BRCA1-related cancers, that are characterized by cytokeratin 5 (CK5) and CK17 expression and show poor prognosis. We assessed Annexin A8's contribution to the overall prognosis and its expression in normal, benign, and cancerous tissue and addressed Annexin A8's physiologic role in the mammary gland. EXPERIMENTAL DESIGN: Using microarrays and reverse transcription-PCR, the Annexin A8 expression was studied during mouse mammary gland development and in isolated mammary structures. Reverse transcription-PCR on cultured human luminal and basal cells, along with immunocytochemistry on normal and benign breast tissues, was used for cellular localization. Annexin A8's prognostic relevance and its coexpression with CK5 were assessed on tissue arrays of 1,631 cases of invasive breast cancer. Coexpression was further evaluated on a small cohort of 14 BRCA1-related breast cancers. RESULTS: Annexin A8 was up-regulated during mouse mammary gland involution and in pubertal ductal epithelium. Annexin A8 showed preferred expression in cultured basal cells but predominant luminal expression in normal human breast tissue in vivo. Hyperplasias and in situ carcinomas showed a strong staining of basal cells. Annexin A8 expression was significantly associated with grade (P < 0.0001), CK5 (P < 0.0001), and estrogen receptor status (P < 0.0001); 85.7% BRCA1-related breast tumors coexpressed Annexin A8 and CK5. CONCLUSION: Annexin A8 is involved in mouse mammary gland involution. In humans, it is a luminally expressed protein with basal expression in cell culture and in hyperplasia/ductal carcinoma in situ. Expression in invasive breast carcinomas has a significant effect on survival (P = 0.03) but is not independent of grade or CK5.


Subject(s)
Annexins/biosynthesis , Breast Neoplasms/metabolism , Breast Neoplasms/mortality , Gene Expression Regulation, Neoplastic , Mammary Glands, Animal/metabolism , Mammary Glands, Animal/pathology , Up-Regulation , Animals , Apoptosis , Carcinoma/metabolism , Carcinoma/pathology , Carcinoma, Intraductal, Noninfiltrating/pathology , Cohort Studies , Female , Genes, BRCA1 , Humans , Immunohistochemistry , Keratins/biosynthesis , Mice , Mutation , Oligonucleotide Array Sequence Analysis , Oligonucleotides/chemistry , Phenotype , Polymerase Chain Reaction , Prognosis , RNA/chemistry , Reverse Transcriptase Polymerase Chain Reaction , Time Factors , Treatment Outcome
13.
Ann Surg ; 242(2): 188-92, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16041208

ABSTRACT

OBJECTIVE: Prospectively evaluate whether for patients having laparoscopic cholecystectomy with failed trans-cystic duct clearance of bile duct (BD) stones they should have laparoscopic choledochotomy or postoperative endoscopic retrograde cholangiography (ERCP). SUMMARY BACKGROUND DATA: Clinical management of BD stones found at laparoscopic cholecystectomy in the last decade has focused on pre-cholecystectomy detection with ERCP clearance in those with suspected stones. This clinical algorithm successfully clears the stones in most patients, but no stones are found in 20% to 60% of patients and rare unpredictably severe ERCP morbidity can result in this group. Our initial experience of 300 consecutive patients with fluoroscopic cholangiography and intraoperative clearance demonstrated that, for the pattern of stone disease we see, 66% of patients' BD stones can be cleared via the cystic duct with dramatic reduction in morbidity compared to the 33% requiring choledochotomy or ERCP. Given the limitations of the preoperative approach to BD stone clearance, this trial was designed to explore the limitations, for patients failing laparoscopic trans-cystic clearance, of laparoscopic choledochotomy or postoperative ERCP. METHODS: Across 7 metropolitan hospitals after failed trans-cystic duct clearance, patients were intraoperatively randomized to have either laparoscopic choledochotomy or postoperative ERCP. Exclusion criteria were: ERCP prior to referral for cholecystectomy, severe cholangitis or pancreatitis requiring immediate ERCP drainage, common BD diameter of less than 7 mm diameter, or if bilio-enteric drainage was required in addition to stone clearance. Drain decompression of the cleared BD was used in the presence of cholangitis, an edematous ampulla due to instrumentation or stone impaction and technical difficulties from local inflammation and fibrosis. The ERCP occurred prior to discharge from hospital. Mechanical and extracorporeal shockwave lithotripsy was available. Sphincter balloon dilation as an alternative to sphincterotomy to allow stone extraction was not used. Major endpoints for the trial were operative time, morbidity, retained stone rate, reoperation rate, and hospital stay. RESULTS: From June 1998 to February 2003, 372 patients with BD stones had successful trans-cystic duct clearance of stones in 286, leaving 86 patients randomized into the trial. Total operative time was 10.9 minutes longer in the choledochotomy group (158.8 minutes), with slightly shorter hospital stay 6.4 days versus 7.7 days. Bile leak occurred in 14.6% of those having choledochotomy with similar rates of pancreatitis (7.3% versus 8.8%), retained stones (2.4% versus 4.4%), reoperation (7.3% versus 6.6%), and overall morbidity (17% versus 13%). CONCLUSIONS: These data suggest that the majority of secondary BD stones can be diagnosed at the time of cholecystectomy and cleared trans-cystically, with those failing having either choledochotomy or postoperative ERCP. However, because of the small trial size, a significant chance exists that small differences in outcome may exist. We would avoid choledochotomy in ducts less than 7 mm measured at the time of operative cholangiogram and severely inflamed friable tissues leading to a difficult dissection. We would advocate choledochotomy as a good choice for patients after Billroth 11 gastrectomy, failed ERCP access, or where long delays would occur for patient transfer to other locations for the ERCP.


Subject(s)
Cholangiopancreatography, Endoscopic Retrograde , Common Bile Duct/surgery , Gallstones/therapy , Adolescent , Adult , Aged , Cholangiography , Cholecystectomy, Laparoscopic , Female , Humans , Laparoscopy , Male , Middle Aged , Prospective Studies , Treatment Outcome
14.
J Natl Med Assoc ; 97(4): 467-77, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15868767

ABSTRACT

BACKGROUND: In response to a growing concern regarding physician discrimination in the workplace, this study was developed to: (1) describe the types of discrimination that exist for the practicing physician and (2) determine which groups of physicians are more likely to experience the various forms of discrimination. METHODS: Surveys were mailed to 1930 practicing physicians in Massachusetts. Participants were asked if they had encountered discrimination, how significant the discrimination was against a specific group, the frequency of personal discrimination, and the type of discrimination. Factor analysis identified four types of discrimination: career advancement, punitive behaviors, practice barriers and hiring barriers. RESULTS: A total of 445 responses were received (a 24% response rate). Sixty-three percent of responding physicians had experienced some form of discrimination. Respondents were women (46%), racial/ethnic minorities (42%) and international medical graduates (IMGs) (40%). In addition, 26% of those classified as white were also IMGs. Over 60% of respondents believed discrimination against IMGs was very or somewhat significant. Almost 27% of males acknowledged that gender bias against females was very or somewhat significant. IMGs were more likely to indicate that discrimination against IMGs was significant in their current organization. Of U.S. medical graduates (USMGs) 44% reported that discrimination against IMGs in their current organization was significant. Nonwhites were more likely to report that discrimination based on race/ethnicity was significant. Nearly 29% of white respondents also believed that such discrimination was very or somewhat significant. CONCLUSIONS: Physicians practicing in academic, research, and private practice sectors experience discrimination based on gender, ethnic/racial, and IMG status.


Subject(s)
Ethnicity/statistics & numerical data , Foreign Medical Graduates/statistics & numerical data , Interprofessional Relations , Job Satisfaction , Physicians/statistics & numerical data , Prejudice , Workplace , Adult , Aged , Attitude of Health Personnel , Cultural Diversity , Female , Foreign Medical Graduates/psychology , Health Care Surveys , Humans , Male , Massachusetts , Middle Aged , Organizational Innovation , Physicians/classification , Physicians/psychology , Physicians, Women/psychology , Sex Factors , Surveys and Questionnaires
15.
J Child Neurol ; 19(3): 214-8, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15119482

ABSTRACT

Joubert syndrome is an autosomal recessive disorder characterized by hypotonia, ataxia, developmental delay, and a distinctive hindbrain malformation involving the cerebellum and brain stem, visualized radiographically on magnetic resonance imaging (MRI) as the "molar tooth sign." In postmortem brains from subjects with Joubert syndrome, there is an apparent absence of decussation of both corticospinal and superior cerebellar tracts, although the functional significance has not been elucidated. We sought to explore the cerebral and cerebellar activation pattern elicited by finger tapping in an adolescent with Joubert syndrome and in a normal control subject using functional MRI. In contrast to the typical highly lateralized activation seen in our control subject, the subject with Joubert syndrome demonstrated striking bilateral activation of the sensorimotor and cerebellar cortex. Although our functional MRI data do not indicate a clear absence of decussation, the abnormal activation pattern observed suggests altered brain functional organization in relation to anatomic differences. Malformation of the hindbrain could result in recruitment of alternative pathways, similar to what has been observed following ischemic injury to the developing or mature central nervous system.


Subject(s)
Brain Stem/abnormalities , Cerebellum/abnormalities , Cerebellum/physiopathology , Cerebral Cortex/physiopathology , Chromosome Aberrations , Genes, Recessive/genetics , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Motor Activity/physiology , Spinocerebellar Degenerations/diagnosis , Spinocerebellar Degenerations/genetics , Adolescent , Adult , Brain Mapping , Brain Stem/physiopathology , Child , Dominance, Cerebral/genetics , Dominance, Cerebral/physiology , Female , Follow-Up Studies , Humans , Motor Cortex/physiopathology , Pyramidal Tracts/abnormalities , Pyramidal Tracts/physiopathology , Recruitment, Neurophysiological/physiology , Reference Values , Somatosensory Cortex/physiopathology , Syndrome
16.
Neuropsychology ; 18(2): 232-9, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15099145

ABSTRACT

Twenty-one pairs of monozygotic twins discordant for chronic fatigue syndrome (CFS) and 21 matched healthy control (HC) subjects were assessed with 5 untimed tests and 5 timed tests from the computer-based NeuroCognitive Assessment Battery (R. K. Mahurin, 1993). Random effects regression showed no difference between CFS and healthy twins on any of the cognitive tests. Further, the twin groups did not differ from the HC group on any content-dependent measure. In contrast, both sets of twins performed worse than the HC group on all speed-dependent tests except Finger Tapping. Self-rated fatigue and dysphoric mood were only weakly correlated with cognitive performance. These data point toward a shared genetic trait related to information processing that is manifest in the CFS context. The findings have implications for differentiating genetic and acquired vulnerability in the symptomatic expression of the disorder. ((c) 2004 APA, all rights reserved)


Subject(s)
Cognition Disorders/genetics , Diseases in Twins , Fatigue Syndrome, Chronic/genetics , Neuropsychological Tests/statistics & numerical data , Adult , Cognition Disorders/psychology , Color Perception , Discrimination Learning , Fatigue Syndrome, Chronic/psychology , Female , Humans , Individuality , Logic , Male , Memory, Short-Term , Middle Aged , Pattern Recognition, Visual , Phenotype , Problem Solving , Psychometrics/statistics & numerical data , Reaction Time/genetics , Reference Values , Reproducibility of Results , Twins, Monozygotic/psychology , Verbal Learning
17.
Breast Cancer Res ; 6(2): R75-91, 2004.
Article in English | MEDLINE | ID: mdl-14979920

ABSTRACT

INTRODUCTION: Involution of the mammary gland is a complex process of controlled apoptosis and tissue remodelling. The aim of the project was to identify genes that are specifically involved in this process. METHODS: We used Affymetrix oligonucleotide microarrays to perform a detailed transcript analysis on the mechanism of controlled involution after withdrawal of the pups at day seven of lactation. Some of the results were confirmed by semi-quantitative reverse transcriptase polymerase chain reaction, Western blotting or immunohistochemistry. RESULTS: We identified 145 genes that were specifically upregulated during the first 4 days of involution; of these, 49 encoded immunoglobulin genes. A further 12 genes, including those encoding the signal transducer and activator of transcription 3 (STAT3), the lipopolysaccharide receptor (CD14) and lipopolysaccharide-binding protein (LBP), were involved in the acute-phase response, demonstrating that the expression of acute-phase response genes can occur in the mammary gland itself and not only in the liver. Expression of LBP and CD14 was upregulated, at both the RNA and protein level, immediately after pup withdrawal; CD14 was strongly expressed in the luminal epithelial cells. Other genes identified suggested neutrophil activation early in involution, followed by macrophage activation late in the process. Immunohistochemistry and histological staining confirmed the infiltration of the involuting mammary tissue with neutrophils, plasma cells, macrophages and eosinophils. CONCLUSION: Oligonucleotide microarrays are a useful tool for identifying genes that are involved in the complex developmental process of mammary gland involution. The genes identified are consistent with an immune cascade, with an early acute-phase response that occurs in the mammary gland itself and resembles a wound healing process.


Subject(s)
Acute-Phase Proteins/genetics , Acute-Phase Reaction/genetics , Carrier Proteins/genetics , DNA-Binding Proteins/genetics , Gene Expression Regulation/genetics , Immune System/metabolism , Lipopolysaccharide Receptors/genetics , Mammary Glands, Animal/chemistry , Mammary Glands, Animal/metabolism , Membrane Glycoproteins/genetics , Trans-Activators/genetics , Animals , Eosinophils/physiology , Epithelial Cells/chemistry , Epithelial Cells/metabolism , Female , Gene Expression Profiling/methods , Gene Expression Regulation/immunology , Infections/genetics , Lymphocytes/physiology , Macrophage Activation/genetics , Mammary Glands, Animal/cytology , Mice , Neutrophil Activation/genetics , Oligonucleotide Array Sequence Analysis/methods , STAT3 Transcription Factor
18.
J Am Geriatr Soc ; 51(12): 1735-9, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14687351

ABSTRACT

OBJECTIVES: To measure the magnitude and prevalence of motor overflow to the arm at rest during attempted unilateral arm movements. DESIGN: Cross-sectional assessment. SETTING: Motor physiology laboratory. PARTICIPANTS: Healthy young (n=20) and elderly (n=20) adult subjects. MEASUREMENTS: Surface electromyography (EMG) was obtained from bilateral forearm muscles during performance of 12 different unilateral finger-tapping tasks. RESULTS: For all subjects, faster movement rate (F=2.56-3.30, P<.05), cognitive distraction (F=4.09, P<.05), and fatigue (F=15.15, P<.001) were each associated with a significant increase in the magnitude of EMG in the arm intended to be at rest. In elderly subjects, tapping at maximum rate and fatigue were each associated with a further increase in motor overflow across the midline. In addition, better left hand dexterity correlated with greater motor overflow to the right hand during rapid left hand tapping (r=0.63, P<.005). Prevalence of motor overflow was also higher in older subjects for some tasks, for example during 1 Hz tapping by the right index finger (motor overflow present in 45%, vs 15% young subjects, P<.05). CONCLUSION: Several behavioral variables increase motor overflow across the midline in young and elderly adults. Motor overflow was even greater in elderly subjects with the most demanding tasks and was greater in those with better motor status, suggesting that this form of motor system change is a compensatory event of normal aging rather than age-related dysfunction. The results support the hypotheses that healthy aging is associated with an increase in the degree to which brain function is bilaterally organized.


Subject(s)
Aging/physiology , Fingers , Hyperkinesis/epidemiology , Adult , Aged , Cross-Sectional Studies , Electric Stimulation , Electromyography , Functional Laterality/physiology , Humans , Hyperkinesis/diagnosis , Hyperkinesis/physiopathology , Prevalence
20.
Immunology ; 108(3): 329-37, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12603599

ABSTRACT

Polymorphonuclear neutrophils (PMNs) are capable of synthesizing various pro-inflammatory cytokines which may indirectly influence specific immune responses. PMNs may also have the capacity to present foreign peptides to helper T cells (Th cells). In support of this hypothesis, recent studies have shown that neutrophils, when activated by the correct combination of cytokines, can be induced to express cell surface major histocompatibility complex (MHC) Class II (DR) antigen, CD80 (B7.1) and CD86 (B7.2): molecules required for antigen presentation and subsequent T-cell activation. In this study we have used normal "resting" human peripheral blood neutrophils and demonstrated, using a mild fixation and permeabilization protocol, significant cytoplasmic "stores" of these molecules known to be important in antigen presentation. Cytoplasmic MHC Class II antigen was found with two out of 20 normal donors tested whereas cytoplasmic CD80 and CD86 were found to a variable extent within all normal donors. Surprisingly, we also found several other neutrophil cytoplasmic CD antigens more commonly associated with B cells, i.e. CD20, CD21 (CR2/EBV-R) and CD22 (BL-CAM). All of these antigens were confined to the "resting" cell cytoplasm and were never found to be expressed on the cell surface. To exclude the possibility that these antigens were absorbed from plasma and to provide evidence for active synthesis, we used a novel whole blood in situ hybridization flow cytometry assay method to detect mRNA specific for these antigens within normal PMNs. We also conducted real-time polymerase chain reactions to confirm these findings using CD22 as a good example of an "inappropriately expressed" CD antigen. These observations therefore provide support for the hypothesis that human PMNs have the potential to express molecules required for antigen presentation and cell signalling.


Subject(s)
Antigens, CD/blood , Cell Adhesion Molecules , Cytoplasm/immunology , Neutrophils/immunology , Antigen Presentation/immunology , Antigens, CD/genetics , Antigens, Differentiation, B-Lymphocyte/blood , Flow Cytometry/methods , Humans , In Situ Hybridization/methods , Lectins/blood , Polymerase Chain Reaction/methods , RNA, Messenger/genetics , Sialic Acid Binding Ig-like Lectin 2
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