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1.
Acta Psychiatr Scand ; 121(2): 119-24, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19573050

ABSTRACT

OBJECTIVE: The amygdala plays a major role in processing emotional stimuli. Fourteen studies using structural magnetic resonance imaging (MRI) have examined the amygdala volume in paediatric and adult patients with bipolar disorder (BD) compared with healthy controls (HC) and reported inconsistent findings. Lithium has been found to increase grey matter volume, and first evidence points towards an effect on regional brain volume such as the amygdala. METHOD: We examined the amygdala volume of euthymic patients with BD treated with lithium (n = 15), without lithium (n = 24) and HC (n = 41) using structural MRI. RESULTS: Patients treated with lithium exhibited in comparison to HC a larger right absolute (+17.9%, P = 0.015) and relative (+18%, P = 0.017) amygdala volume. There was no significant difference in amygdala volume between patients without lithium treatment and HC. CONCLUSION: Lithium appears to have a sustained effect on a central core region of emotional processing and should therefore be considered in studies examining BD.


Subject(s)
Amygdala/anatomy & histology , Antimanic Agents/therapeutic use , Bipolar Disorder/drug therapy , Functional Laterality/physiology , Lithium Carbonate/therapeutic use , Adult , Bipolar Disorder/epidemiology , Cross-Sectional Studies , Depressive Disorder, Major/diagnosis , Depressive Disorder, Major/epidemiology , Diagnostic and Statistical Manual of Mental Disorders , Female , Humans , Magnetic Resonance Imaging , Male
2.
Acta Radiol ; 50(8): 902-8, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19707908

ABSTRACT

BACKGROUND: Somatostatin receptor (SSTR) scintigraphy with (99m)Tc-depreotide is used for differential diagnosis of solitary pulmonary nodules. The method is based on SSTR expression in cancer tissue. PURPOSE: To estimate the expression of SSTRs in non-small-cell lung cancer (NSCLC) in vitro, and to determine the correlation between (99m)Tc-depreotide uptake in vivo and different tumor characteristics determined in vitro, such as tumor grade, and presence of SSTR2, MIB-1, and p53. MATERIAL AND METHODS: A total of 127 patients with lung lesions detected on computed tomography (CT) were investigated with SSTR scintigraphy after injection of 740 MBq (99m)Tc-depreotide. This study includes 19 patients with NSCLC with histologically proven diagnosis. The quantitative evaluation of (99m)Tc-depreotide was performed using region-of-interest analysis and includes tumor counts/cm(3), background counts/cm(3), and the ratio between tumor and background counts. RESULTS: 99mTc-depreotide uptake was found in all NSCLC tumors, which expressed SSTR2 defined in vitro by immunochemical methods. SSTR2 expression was negatively correlated to the degree of the tumor's differentiation (P<0.05). 99mTc-depreotide uptake in tumor cells did not correlate with tumor grade, or SSTR2, MIB-1, or p53 expression. CONCLUSION: There is an expression of SSTRs in NSCLC. The degree of tumor differentiation correlates negatively with SSTR2 measured in vitro and positively with MIB-1 expression in tumor tissue. No correlation was found between (99m)Tc-depreotide uptake and possible prognostic factors such as MIB-1 and p53 expression in tumor cells in NSCLC. Lastly, no correlation was found between (99m)Tc-depreotide uptake and tumor grade or SSTR2 expression.


Subject(s)
Carcinoma, Non-Small-Cell Lung/diagnostic imaging , Lung Neoplasms/diagnostic imaging , Organotechnetium Compounds/pharmacokinetics , Somatostatin/analogs & derivatives , Adult , Aged , Aged, 80 and over , Carcinoma, Non-Small-Cell Lung/metabolism , Carcinoma, Non-Small-Cell Lung/pathology , Carcinoma, Non-Small-Cell Lung/surgery , Diagnosis, Differential , Female , Humans , Immunoenzyme Techniques , Lung Neoplasms/metabolism , Lung Neoplasms/pathology , Lung Neoplasms/surgery , Male , Middle Aged , Radionuclide Imaging , Receptors, Somatostatin/metabolism , Somatostatin/pharmacokinetics
3.
Dev Biol ; 230(1): 74-88, 2001 Feb 01.
Article in English | MEDLINE | ID: mdl-11161563

ABSTRACT

In the embryonic visual system, EphA receptors are expressed on both temporal and nasal retinal ganglion cell axons. Only the temporal axons, however, are sensitive to the low concentrations of ephrin-A ligands found in the anterior optic tectum. The poor responsiveness of nasal axons to ephrin-A ligands, which allows them to traverse the anterior tectum and reach their targets in the posterior tectum, has been attributed to constitutive activation of the EphA4 receptor expressed in these axons. EphA4 is highly expressed throughout the retina, but is preferentially phosphorylated on tyrosine (activated) in nasal retina. In a screen for EphA4 ligands expressed in chicken embryonic retina, we have identified a novel ephrin, ephrin-A6. Like ephrin-A5, ephrin-A6 has high affinity for EphA4 and activates this receptor in cultured retinal cells. In the embryonic day 8 (E8) chicken visual system, ephrin-A6 is predominantly expressed in the nasal retina and ephrin-A5 in the posterior tectum. Thus, ephrin-A6 has the properties of a ligand that activates the EphA4 receptor in nasal retinal cells. Ephrin-A6 binds with high affinity to several other EphA receptors as well and causes growth cone collapse in retinal explants, demonstrating that it can elicit biological responses in retinal neurons. Ephrin-A6 expression is high at E6 and E8, when retinal axons grow to their tectal targets, and gradually declines at later developmental stages. The asymmetric distribution of ephrin-A6 in retinal cells, and the time course of its expression, suggest that this new ephrin plays a role in the establishment of visual system topography.


Subject(s)
Fetal Proteins/metabolism , Membrane Proteins/metabolism , Proteins/metabolism , Receptor Protein-Tyrosine Kinases/metabolism , Retinal Ganglion Cells/metabolism , Superior Colliculi/embryology , Superior Colliculi/metabolism , Amino Acid Sequence , Animals , Base Sequence , Chick Embryo , Cloning, Molecular , DNA Primers/genetics , DNA, Complementary/genetics , Ephrin-A5 , Gene Expression , Ligands , Membrane Proteins/genetics , Molecular Sequence Data , Proteins/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptor, EphA4 , Reverse Transcriptase Polymerase Chain Reaction , Sequence Homology, Amino Acid
4.
Mayo Clin Proc ; 76(2): 134-7, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11213300

ABSTRACT

OBJECTIVE: To determine the attitudes of Olmsted County, Minnesota, adults about environmental tobacco smoke in restaurants, bars, and nightclubs. SUBJECTS AND METHODS: In this population survey,2014 adults were contacted by random digit dial methods between February 28 and May 5, 2000, and asked to participate in a telephone survey; 1224 (61%) consented. RESULTS: For the 57% (95% confidence interval [CI], 54%-60%) of the study population that reported exposure to environmental tobacco smoke, the most frequently reported sites of exposure were restaurants (44% [95% CI, 41%-48%]), work (21% [95% CI, 18%-24%]), and bars (19% [95% CI, 16%-22%]). Seventy-two percent (95% CI, 69%-74%) of respondents said that they would select a smoke-free restaurant over one where smoking is permitted, and 70% (95% CI, 67%-72%) said that they would select a smoke-free bar over one where smoking is permitted. The majority of respondents said that they would not dine out or visit bars or nightclubs more often or less often if all restaurants, bars, and nightclubs were smoke-free. CONCLUSIONS: Olmsted County residents prefer smoke-free restaurants, bars, and nightclubs.


Subject(s)
Attitude to Health , Restaurants , Tobacco Smoke Pollution , Adult , Aged , Female , Humans , Male , Middle Aged , Minnesota , Public Policy
5.
Mayo Clin Proc ; 75(11): 1153-9, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11075745

ABSTRACT

OBJECTIVE: To establish baseline data for the CardioVision 2020 program, a collaborative project in Olmsted County, Minnesota, organized to reduce cardiovascular disease rates by altering 5 health-related items: (1) eliminating tobacco use and exposure, (2) improving nutrition, (3) increasing physical activity, (4) lowering serum cholesterol level, and (5) controlling blood pressure. SUBJECTS AND METHODS: Data about tobacco use, diet, and physical activity were collected by random digit dial interview and follow-up questionnaire from a sample of the population. Blood pressure data were collected from medical records at Mayo Clinic, and serum cholesterol data were derived from the Mayo Clinic laboratory database. Data were stratified into 6 age groups. RESULTS: A total of 624 women and 608 men responded to the questionnaire. Population blood pressure data were available for 1,956 women and 1,084 men. Population serum cholesterol data were available for 17,042 women and 12,511 men. Except for women in the 30- to 39-year-old age group, less than 10% of the population sampled met 4 or 5 goals. Conversely, about 90% of the population met at least 1 goal, and about 80% met 1, 2, or 3 of the goals. CONCLUSION: The data from the Olmsted County population indicate considerable opportunity to reduce this population's burden of cardiovascular disease.


Subject(s)
Cardiovascular Diseases/prevention & control , Health Behavior , Health Surveys , Adult , Aged , Blood Pressure , Cholesterol/blood , Female , Humans , Life Style , Male , Middle Aged , Minnesota , Risk-Taking
6.
Med Care ; 38(9): 892-901, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10982111

ABSTRACT

OBJECTIVE: Before cost-effectiveness analysis (CEA) can fulfill its promise as a tool to guide health care allocation decisions, the method of incorporating societal values into CEA may need to be improved. DESIGN: The study design was a declarative exposition of potential fallacies in the theoretical underpinnings of CEA. Two values held by many people-preferences for giving priority to severely ill patients and preferences to avoid discrimination against people who have limited treatment potential because of disability or chronic illness-that are not currently incorporated into CEA are discussed. CONCLUSIONS: Traditional CEA, through the measurement of quality-adjusted life years (QALYs), is constrained because of a "QALY trap." If, for example, saving the life of a person with paraplegia is equally valuable as saving the life of a person without paraplegia, then current QALY methods force us to conclude that curing paraplegia brings no benefit. Basing cost-effectiveness measurement on societal values rather than QALYs may allow us to better capture public rationing preferences, thereby escaping the QALY trap. CEA can accommodate a wider range of such societal values about fairness in its measurements by amending its methodology.


Subject(s)
Health Care Rationing , Outcome Assessment, Health Care/methods , Quality-Adjusted Life Years , Social Values , Attitude to Health , Chronic Disease , Cost-Benefit Analysis/methods , Disabled Persons , Humans , Outcome Assessment, Health Care/economics , Prejudice , United States , Value of Life
7.
Health Econ ; 9(2): 127-36, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10721014

ABSTRACT

In a previous paper, it was argued that Societal Value measurement through person trade-off (PTO) elicitation offers a way to include the values of both general public and patients into cost-effectiveness analysis (CEA). It was said that patients' values could be used to estimate the effect that various health care dimensions have on health-related utility and that public values could be used to estimate the Societal Value of these changes in utility. However, this previous proposal still creates opportunities for the public to misvalue the benefit of health care interventions because of bias or misunderstanding about what the health-related utility really is of various illnesses or disabilities. A procedure that combines patient and public values into CEA to partially correct for this bias is suggested in this paper. In addition, it is pointed out that, although Societal Value measurement offers a role for distinctly public preferences in CEA, it still does not answer the question of whose utilities ought to be included in CEA.


Subject(s)
Cost-Benefit Analysis , Delivery of Health Care/economics , Humans , Patient Satisfaction , Public Opinion , Quality-Adjusted Life Years , State Medicine , United Kingdom
8.
Mech Dev ; 87(1-2): 119-28, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10495276

ABSTRACT

The formation of the ten cerebellar lobules is an unsolved problem in brain development. We report a screen for the four subfamilies of Eph receptors and their ligands (ephrins) in developing mouse cerebellum, using soluble receptor-immunoglobulin and ligand-immunoglobulin fusion proteins, and antibodies against EphA and ephrin-B proteins. Our results identify Eph receptors and ephrins as the first molecules known to demarcate individual lobules during development. Staining for ephrin-A ligands is in lobule VIII as it forms, across the whole width of the cerebellum. Staining for three EphA receptors approximately coincides with presumptive lobules VI and/or VII before and just after birth, whereas a fourth EphA receptor (EphA4, which binds ligands of both subfamilies) has more widespread expression. Staining for EphB receptors is in lobules VII, VIII, and IX. Staining for ephrin-B ligands is much weaker, becomes detectable only after birth, and does not appear to be lobule-specific. Staining for all subfamilies spreads to at least some adjacent lobules as maturation proceeds. The lobule-specific patterns appear before the lobules form, and initially extend across the width of the cerebellum, in spite of the lesser conservation of the lateral extensions of the lobules. These expression patterns define previously unknown developmental units and suggest that Eph family proteins may contribute to cerebellar morphogenesis.


Subject(s)
Cerebellum/embryology , Cerebellum/metabolism , Membrane Proteins/metabolism , Receptor Protein-Tyrosine Kinases/metabolism , Animals , Ephrin-A2 , Ephrin-A5 , Ephrin-B1 , Epitopes/metabolism , Fetal Proteins/metabolism , Immunoglobulin Fc Fragments/metabolism , Immunohistochemistry , In Situ Hybridization , Mice , Receptor, EphA4 , Receptor, EphA7 , Time Factors , Transcription Factors/metabolism
10.
Health Econ ; 8(1): 25-39, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10082141

ABSTRACT

The paper addresses some limitations of the QALY approach and outlines a valuation procedure that may overcome these limitations. In particular, we focus on the following issues: the distinction between assessing individual utility and assessing societal value of health care; the need to incorporate concerns for severity of illness as an independent factor in a numerical model of societal valuations of health outcomes; similarly, the need to incorporate reluctance to discriminate against patients that happen to have lesser potentials for health than others; and finally, the need to combine measurements of health-related quality of life obtained from actual patients (or former patients) with measurements of distributive preferences in the general population when estimating societal value. We show how equity weights may serve to incorporate concerns for severity and potentials for health in QALY calculations. We also suggest that for chronically ill or disabled people a life year gained should count as one and no less than one as long as the year is considered preferable to being dead by the person concerned. We call our approach 'cost-value analysis'.


Subject(s)
Health Care Rationing , Health Services Research/economics , Program Evaluation/economics , Quality-Adjusted Life Years , Social Justice , Cost-Benefit Analysis , Health Services Research/methods , Humans , Models, Theoretical , Program Evaluation/methods , Severity of Illness Index , Social Values
11.
JAMA ; 281(3): 228; author reply 228-9, 1999 Jan 20.
Article in English | MEDLINE | ID: mdl-9918470
12.
Protein Eng ; 11(10): 937-40, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9862214

ABSTRACT

Basic fibroblast growth factor (bFGF) is implicated in the pathogenesis of several types of vascular and connective diseases. A key step in the discovery of bFGF receptor antagonists to mitigate these actions is to define the functional epitopes required for receptor binding of the growth factor. Using structure-based site-directed mutagenesis, two critical areas on the bFGF surface for the high affinity receptor binding have already been identified [Springer, B.A., Pantoliano, M.W., Barberal, F.A., Gunyuzlu, P.L., Thompson, L.D., Herblin, W.F., Rosenfeld, S.A. and Book, G.W. (1994) J. Biol. Chem., 269, 26879-26884; Zhu, H.Y., Ramnarayan, K., Anchin, J., Miao, Y., Sereno, A., Millman, L., Zheng, J., Balaji, V.N. and Wolff, M.E. (1995) J. Biol. Chem., 270, 21869-21874; Zhu, H.Y., Anchin, J., Ramnarayan, K., Zheng, J., Kawai, T., Mong, S. and Wolff, M.E. (1997) Protein Engng, 10, 417-421]. According to these studies, one receptor binding site includes two polar residues Glu96 and Asn104 on bFGF whereas the other includes four hydrophobic residues Tyr24, Tyr103, Leu140 and Met142. Using a protein modelling technique, we report here the identification of a new hydrophobic patch on bFGF which includes residues Tyr73, Val88 and Phe93. The role of this area on receptor binding affinity was evaluated by mutating each of these residues individually and determining the mutated protein's (mutein's) receptor binding affinity. In addition, we examined the role of two other hydrophobic residues, Phe30 and Leu138, on bFGF for high-affinity receptor binding. These two residues are the neighbors of the hydrophobic residues Tyr24 and Tyr103, respectively. Replacement of Val88 and Phe93 with alanine reduced the receptor binding affinity about 10- and 80-fold, respectively, compared with wild-type bFGF. In contrast, substitution of Phe30 and Leu138 with alanine has no effect on the receptor binding affinities. We conclude that the newly identified hydrophobic residues, Val88 and Phe93, are crucial for the receptor binding. The present data, together with the previous identification of four hydrophobic residues (Tyr24, Tyr103, Leu140 and Met142), suggests that there are two hydrophobic receptor binding sites on the bFGF surface. Our findings can be employed in the discovery and design of potent bFGF antagonists using computational methods.


Subject(s)
Amino Acids/metabolism , Fibroblast Growth Factor 2/metabolism , Mutagenesis, Site-Directed , Receptors, Fibroblast Growth Factor/metabolism , Amino Acid Substitution , Amino Acids/genetics , Binding, Competitive , Chromatography, Liquid , Cytoplasm/metabolism , Fibroblast Growth Factor 2/chemistry , Fibroblast Growth Factor 2/genetics , Fibroblast Growth Factor 2/isolation & purification , Humans , Inclusion Bodies , Leucine/genetics , Leucine/metabolism , Models, Molecular , Phenylalanine/genetics , Phenylalanine/metabolism , Protein Conformation , Recombinant Proteins/chemistry , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Solubility , Solvents , Tyrosine/genetics , Tyrosine/metabolism , Valine/genetics , Valine/metabolism
14.
Dev Biol ; 193(1): 21-35, 1998 Jan 01.
Article in English | MEDLINE | ID: mdl-9466885

ABSTRACT

The EphA3 receptor tyrosine kinase has been implicated in guiding the axons of retinal ganglion cells as they extend in the optic tectum. A repulsive mechanism involving opposing gradients of the EphA3 receptor on retinal axons and its ligands, ephrin-A2 and ephrin-A5, in the tectum influences topographic mapping of the retinotectal projection. To investigate the overall role of the Eph family in patterning of the visual system, we have used in situ hybridization to localize nine Eph receptors in the chicken retina and optic tectum at Embryonic Day 8. Three of the receptors examined correspond to the novel chicken homologs of EphA2, EphA6, and EphA7. Unexpectedly, we found that many Eph receptors are expressed not only in retinal ganglion cells, but also in tectal cells, In particular, EphA3 mRNA is prominently expressed in the anterior tectum, with a pattern reciprocal to that of ephrin-A2 and ephrin-A5. Similarly, ephrin-A5 is expressed not only in tectal cells but also in the nasal retina, with a pattern reciprocal to that of its receptor EphA3 and partially overlapping with that of its other receptor EphA4. Consistent with the even distribution of EphA4 and the polarized distribution of EphA4 ligands in the retina, probing EphA4 immunoprecipitates from different sectors of the retina with anti-phosphotyrosine antibodies revealed spatial differences in receptor phosphorylation. These complex patterns of expression and tyrosine phosphorylation suggest that Eph receptors and ephrins contribute to establishing topography of retinal axons through multiple mechanisms, in addition to playing a role in intraretinal and intratectal organization.


Subject(s)
Receptor Protein-Tyrosine Kinases/genetics , Receptor Protein-Tyrosine Kinases/metabolism , Retina/embryology , Superior Colliculi/embryology , Tyrosine/metabolism , Amino Acid Sequence , Animals , Base Sequence , Body Patterning , Chick Embryo , Gene Expression Regulation, Developmental , In Situ Hybridization/methods , Ligands , Molecular Sequence Data , Phosphorylation , RNA Probes , RNA, Messenger/analysis , Receptor Protein-Tyrosine Kinases/analysis , Retina/chemistry , Sequence Analysis, DNA , Superior Colliculi/chemistry
18.
Hum Gene Ther ; 5(9): 1079-88, 1994 Sep.
Article in English | MEDLINE | ID: mdl-7833367

ABSTRACT

We have constructed recombinant human adenoviruses that express wild-type human p53 under the control of either the Ad 2 major late promoter (MLP) or the human cytomegalovirus (CMV) immediate early gene promoter. Each construct replaces the Ad 5 E1a and E1b coding sequences necessary for viral replication with the p53 cDNA and MLP or CMV promoter. These p53/Ad recombinants are able to express p53 protein in a dose-dependent manner in infected human cancer cells. Tumor suppressor activity of the expressed p53 protein was assayed by several methods. [3H]Thymidine incorporation assays showed that the recombinant adenoviruses were capable of inhibiting DNA synthesis in a p53-specific, dose-dependent fashion. Ex vivo treatment of Saos-2 tumor cells, followed by injection of the treated cells into nude mice, led to complete tumor suppression using the MLP/p53 recombinant. Following a single injection of CMV/p53 recombinant adenovirus into the peritumoral space surrounding an in vivo established tumor derived from a human small cell lung carcinoma cell line (NIH-H69), we were able to detect p53 mRNA in the tumors at 2 and 7 days post-injection. Continued treatment of established H69 tumors with MLP/p53 recombinant led to reduced tumor growth and increased survival time compared to control treated animals. These results indicate that recombinant adenoviruses expressing wild-type p53 may be useful vectors for gene therapy of human cancer.


Subject(s)
Adenoviruses, Human/genetics , Carcinoma, Small Cell/therapy , Defective Viruses/genetics , Genes, p53 , Genetic Therapy , Genetic Vectors , Neoplasms/therapy , Animals , Base Sequence , Carcinoma, Small Cell/pathology , Cytomegalovirus/genetics , DNA Replication , DNA, Complementary/genetics , DNA, Recombinant/genetics , DNA, Viral/genetics , Female , Humans , Lung Neoplasms/pathology , Mice , Mice, Inbred BALB C , Mice, Nude , Molecular Sequence Data , Neoplasm Transplantation , Neoplasms/genetics , Promoter Regions, Genetic , Recombinant Fusion Proteins , Transplantation, Heterologous , Tumor Cells, Cultured , Tumor Suppressor Protein p53/deficiency , Tumor Suppressor Protein p53/genetics
20.
Health Care Anal ; 2(1): 13-22, 1994 Feb.
Article in English | MEDLINE | ID: mdl-10134366

ABSTRACT

This paper offers a relatively comprehensive assessment of government anti-smoking policies (both taxation and other regulatory measures). I conclude that interventions to engender in smokers and prospective smokers an accurate perception of tobacco's health risks are justified, that except in the case of adolescents addiction by itself does not justify intervention beyond providing adequate information, that the proper goal of tobacco taxation policy should be to recoup only the extra costs that smokers place on others (at most a $1/pack tax on cigarettes), and that passive smoke's imposition of harm on unconsenting others strongly supports at least the development of a safe-to-others smokeless cigarette, if not direct intervention.


Subject(s)
Health Promotion/methods , Public Policy , Smoking Prevention , Attitude to Health , Choice Behavior , Cost-Benefit Analysis , Health Behavior , Health Promotion/economics , Humans , Plants, Toxic , Risk , Smoking/adverse effects , Smoking/economics , Taxes/legislation & jurisprudence , Tobacco Smoke Pollution/adverse effects , Tobacco Smoke Pollution/economics , Tobacco Smoke Pollution/prevention & control , Tobacco, Smokeless , United States
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