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1.
R Soc Open Sci ; 10(3): 221503, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36968239

ABSTRACT

The rate at which zoonotic viruses spill over into the human population varies significantly over space and time. Remarkably, we do not yet know how much of this variation is attributable to genetic variation within viral populations. This gap in understanding arises because we lack methods of genetic analysis that can be easily applied to zoonotic viruses, where the number of available viral sequences is often limited, and opportunistic sampling introduces significant population stratification. Here, we explore the feasibility of using patterns of shared ancestry to correct for population stratification, enabling genome-wide association methods to identify genetic substitutions associated with spillover into the human population. Using a combination of phylogenetically structured simulations and Lassa virus sequences collected from humans and rodents in Sierra Leone, we demonstrate that existing methods do not fully correct for stratification, leading to elevated error rates. We also demonstrate, however, that the Type I error rate can be substantially reduced by confining the analysis to a less-stratified region of the phylogeny, even in an already-small dataset. Using this method, we detect two candidate single-nucleotide polymorphisms associated with spillover in the Lassa virus polymerase gene and provide generalized recommendations for the collection and analysis of zoonotic viruses.

2.
Lancet Microbe ; 3(8): e625-e637, 2022 08.
Article in English | MEDLINE | ID: mdl-35036970

ABSTRACT

Despite the global investment in One Health disease surveillance, it remains difficult and costly to identify and monitor the wildlife reservoirs of novel zoonotic viruses. Statistical models can guide sampling target prioritisation, but the predictions from any given model might be highly uncertain; moreover, systematic model validation is rare, and the drivers of model performance are consequently under-documented. Here, we use the bat hosts of betacoronaviruses as a case study for the data-driven process of comparing and validating predictive models of probable reservoir hosts. In early 2020, we generated an ensemble of eight statistical models that predicted host-virus associations and developed priority sampling recommendations for potential bat reservoirs of betacoronaviruses and bridge hosts for SARS-CoV-2. During a time frame of more than a year, we tracked the discovery of 47 new bat hosts of betacoronaviruses, validated the initial predictions, and dynamically updated our analytical pipeline. We found that ecological trait-based models performed well at predicting these novel hosts, whereas network methods consistently performed approximately as well or worse than expected at random. These findings illustrate the importance of ensemble modelling as a buffer against mixed-model quality and highlight the value of including host ecology in predictive models. Our revised models showed an improved performance compared with the initial ensemble, and predicted more than 400 bat species globally that could be undetected betacoronavirus hosts. We show, through systematic validation, that machine learning models can help to optimise wildlife sampling for undiscovered viruses and illustrates how such approaches are best implemented through a dynamic process of prediction, data collection, validation, and updating.


Subject(s)
COVID-19 , Chiroptera , Viruses , Animals , COVID-19/epidemiology , SARS-CoV-2 , Phylogeny
3.
Nat Microbiol ; 6(12): 1483-1492, 2021 12.
Article in English | MEDLINE | ID: mdl-34819645

ABSTRACT

Better methods to predict and prevent the emergence of zoonotic viruses could support future efforts to reduce the risk of epidemics. We propose a network science framework for understanding and predicting human and animal susceptibility to viral infections. Related approaches have so far helped to identify basic biological rules that govern cross-species transmission and structure the global virome. We highlight ways to make modelling both accurate and actionable, and discuss the barriers that prevent researchers from translating viral ecology into public health policies that could prevent future pandemics.


Subject(s)
Host-Pathogen Interactions , Virus Diseases/virology , Virus Physiological Phenomena , Animals , Humans , Virus Diseases/physiopathology , Viruses/genetics , Zoonoses/physiopathology , Zoonoses/virology
5.
Curr Microbiol ; 78(9): 3526-3540, 2021 Sep.
Article in English | MEDLINE | ID: mdl-34318342

ABSTRACT

Microbiota perform vital functions for their mammalian hosts, making them potential drivers of host evolution. Understanding effects of environmental factors and host characteristics on the composition and biodiversity of the microbiota may provide novel insights into the origin and maintenance of these symbiotic relationships. Our goals were to (1) characterize biodiversity of oral and rectal microbiota in bats from Puerto Rico; and (2) determine the effects of geographic location and host characteristics on that biodiversity. We collected bats and their microbiota from three sites, and used four metrics (species richness, Shannon diversity, Camargo evenness, Berger-Parker dominance) to characterize biodiversity. We quantified the relative importance of site, host sex, host species-identity, and host foraging-guild on biodiversity of the microbiota. Microbe biodiversity was highly variable among conspecifics. Geographical location exhibited consistent effects, whereas host sex did not. Within each host guild, host species exhibited consistent differences in biodiversity of oral microbiota and of rectal microbiota. Oral microbe biodiversity was indistinguishable between guilds, whereas rectal microbe biodiversity was significantly greater in carnivores than in herbivores. The high intraspecific and spatial variation in microbe biodiversity necessitate a relatively large number of samples to statistically isolate the effects of environmental or host characteristics on the microbiota. Species-specific biodiversity of oral microbiota suggests these communities are structured by direct interactions with the host immune system via epithelial receptors. In contrast, the number of microbial taxa that a host gut supports may be driven by host diet-diversity or composition.


Subject(s)
Chiroptera , Microbiota , Animals , Biodiversity , Diet , Hispanic or Latino , Humans , Puerto Rico
6.
Nutrients ; 13(3)2021 Mar 02.
Article in English | MEDLINE | ID: mdl-33801247

ABSTRACT

Ketogenic low-carbohydrate high-fat (LCHF) diets are popular among young, healthy, normal-weight individuals for various reasons. We aimed to investigate the effect of a ketogenic LCHF diet on low-density lipoprotein (LDL) cholesterol (primary outcome), LDL cholesterol subfractions and conventional cardiovascular risk factors in the blood of healthy, young, and normal-weight women. The study was a randomized, controlled, feeding trial with crossover design. Twenty-four women were assigned to a 4 week ketogenic LCHF diet (4% carbohydrates; 77% fat; 19% protein) followed by a 4 week National Food Agency recommended control diet (44% carbohydrates; 33% fat; 19% protein), or the reverse sequence due to the crossover design. Treatment periods were separated by a 15 week washout period. Seventeen women completed the study and treatment effects were evaluated using mixed models. The LCHF diet increased LDL cholesterol in every woman with a treatment effect of 1.82 mM (p < 0.001). In addition, Apolipoprotein B-100 (ApoB), small, dense LDL cholesterol as well as large, buoyant LDL cholesterol increased (p < 0.001, p < 0.01, and p < 0.001, respectively). The data suggest that feeding healthy, young, normal-weight women a ketogenic LCHF diet induces a deleterious blood lipid profile. The elevated LDL cholesterol should be a cause for concern in young, healthy, normal-weight women following this kind of LCHF diet.


Subject(s)
Cholesterol, LDL/blood , Diet, Carbohydrate-Restricted , Diet, High-Fat , Adult , Cardiovascular Diseases/etiology , Cholesterol/blood , Fatty Acids , Female , Humans , Lipids/blood , Lipoproteins , Risk Factors , Sweden , Young Adult
7.
PLoS Comput Biol ; 17(3): e1008811, 2021 03.
Article in English | MEDLINE | ID: mdl-33657095

ABSTRACT

Forecasting the risk of pathogen spillover from reservoir populations of wild or domestic animals is essential for the effective deployment of interventions such as wildlife vaccination or culling. Due to the sporadic nature of spillover events and limited availability of data, developing and validating robust, spatially explicit, predictions is challenging. Recent efforts have begun to make progress in this direction by capitalizing on machine learning methodologies. An important weakness of existing approaches, however, is that they generally rely on combining human and reservoir infection data during the training process and thus conflate risk attributable to the prevalence of the pathogen in the reservoir population with the risk attributed to the realized rate of spillover into the human population. Because effective planning of interventions requires that these components of risk be disentangled, we developed a multi-layer machine learning framework that separates these processes. Our approach begins by training models to predict the geographic range of the primary reservoir and the subset of this range in which the pathogen occurs. The spillover risk predicted by the product of these reservoir specific models is then fit to data on realized patterns of historical spillover into the human population. The result is a geographically specific spillover risk forecast that can be easily decomposed and used to guide effective intervention. Applying our method to Lassa virus, a zoonotic pathogen that regularly spills over into the human population across West Africa, results in a model that explains a modest but statistically significant portion of geographic variation in historical patterns of spillover. When combined with a mechanistic mathematical model of infection dynamics, our spillover risk model predicts that 897,700 humans are infected by Lassa virus each year across West Africa, with Nigeria accounting for more than half of these human infections.


Subject(s)
Disease Reservoirs/virology , Lassa Fever , Lassa virus , Models, Biological , Africa, Western , Animals , Animals, Wild/virology , Computational Biology , Ecology , Humans , Lassa Fever/epidemiology , Lassa Fever/transmission , Lassa Fever/veterinary , Lassa Fever/virology , Machine Learning , Models, Statistical , Risk , Rodentia/virology
8.
Nutrients ; 12(4)2020 Mar 30.
Article in English | MEDLINE | ID: mdl-32235518

ABSTRACT

Ketogenic low-carbohydrate high-fat (LCHF) diets are increasingly popular in broad sections of the population. The main objective of this study was to evaluate the effects of a non-energy-restricted ketogenic LCHF diet on muscle fatigue in healthy, young, and normal-weight women. Twenty-four women were randomly allocated to a 4-week ketogenic LCHF diet followed by a 4-week control diet (a National Food Agency recommended diet), or the reverse sequence due to the crossover design. Treatment periods were separated by a 15 week washout period. Seventeen women completed the study and were included in the analyses. Treatment effects were evaluated using mixed models. The ketogenic LCHF diet had no effect on grip strength or time to fatigue, measured with handgrip test (day 24-26). However, cycling time to fatigue decreased with almost two minutes (-1.85 min 95% CI:[-2.30;-1.40]; p < 0.001) during incremental cycling (day 25-27), accommodated with higher ratings of perceived exertion using the Borg scale (p < 0.01). Participants' own diary notes revealed experiences of muscle fatigue during daily life activities, as well as during exercise. We conclude that in young and healthy women, a ketogenic LCHF diet has an unfavorable effect on muscle fatigue and might affect perceived exertion during daily life activities.


Subject(s)
Body Weight/physiology , Diet, Ketogenic/adverse effects , Hand Strength/physiology , Healthy Volunteers , Muscle Fatigue/physiology , Muscle Strength/physiology , Nutritional Physiological Phenomena/physiology , Physical Exertion/physiology , Activities of Daily Living , Adult , Bicycling/physiology , Cross-Over Studies , Female , Humans , Young Adult
9.
Int J Offender Ther Comp Criminol ; 62(10): 3097-3116, 2018 08.
Article in English | MEDLINE | ID: mdl-29121811

ABSTRACT

Furthering knowledge of the subset of incarcerated partner violent offenders distinguished by aggression, anger, and hostility is relevant, as these offenders are guilty of the more severe kinds of intimate partner violence (IPV). Our aim was to identify groups with different patterns of IPV among convicted young Swedish male offenders, using data from the Development of Aggressive Antisocial Behavior Study, including 171 young men (18-25 years) convicted of a violent crime. Cluster analysis was used to identify different clusters based on amount and severity of IPV in combination with measures of anger, hostility, aggression, and psychopathic personality traits. The results point to an association between antisocial development, criminal history, the severity of current crime, and measures of aggression, hostility, and partner abuse. The cluster defined by higher levels of partner abuse and aggression was significantly associated with early onset conduct disorder.


Subject(s)
Aggression , Intimate Partner Violence , Prisoners , Adolescent , Adult , Antisocial Personality Disorder/psychology , Cluster Analysis , Hostility , Humans , Male , Sweden , Young Adult
10.
Article in English | IBECS | ID: ibc-163675

ABSTRACT

The aim of this study was to characterize young dating violent offenders (DVO), and to compare them to the general population and to young offenders with violent crimes directed against other victims. We have used data from the Development of Aggressive Antisocial Behaviour Study, in all 262 young men, 18 to 25 years, convicted of violent crimes and imprisoned in the Western Region of the Swedish Prison and Probation Services. We found that young DVO offenders differed from the general population in all investigated areas; however, the group did not differ in comparisons to other young violent offenders. Our results highlight the antisocial aspects of dating violent crime being rooted in aggressive antisocial behaviour, lacking signs of any specific offender type characteristics, thus questioning the validity of crime specific treatment programs in prison for young offenders of dating violence (AU)


El presente estudio ha tenido por objetivo la caracterización de los jóvenes delincuentes violentos en sus relaciones sentimentales («DVO» en su acrónimo inglés) y su comparación tanto con el conjunto de la población como con otros delincuentes violentos jóvenes que han cometido delitos con otro tipo de víctimas. Hemos empleado datos del estudio sobre desarrollo de conducta antisocial violenta con 262 jóvenes varones de entre 18 y 25 años de edad condenados por delitos violentos y encarcelados en la Región Oeste del Servicio de Prisiones y Libertad Vigilada de Suecia y hallado que los jóvenes delincuentes de tipo DVO se diferenciaban del resto de la población en todas las áreas objeto de estudio. Sin embargo, no mostraban discrepancias con respecto a otros delincuentes violentos jóvenes. Nuestros resul-tados destacan que los aspectos antisociales de los delitos violentos en las relaciones sentimentales tienen su base en una conducta antisocial violenta, sin indicios de vinculación con un tipo específico de delincuentes, lo cual cuestiona la validez de los programas penitenciarios para el tratamiento de delitos específicos orientados a delincuentes jóvenes condenados por violencia en las relaciones sentimentales (AU)


Subject(s)
Humans , Male , Middle Aged , Violence/legislation & jurisprudence , Violence/psychology , Juvenile Delinquency/psychology , Antisocial Personality Disorder/psychology , Aggression , Prisons/legislation & jurisprudence , Intimate Partner Violence/psychology , 28599 , Conduct Disorder/psychology , Substance-Related Disorders/psychology , Prisons/standards
11.
Nutr Metab (Lond) ; 13: 79, 2016.
Article in English | MEDLINE | ID: mdl-27891164

ABSTRACT

BACKGROUND: Excess body fat is a major health issue and a risk factor for the development of numerous chronic diseases. Low-carbohydrate diets like the Atkins Diet are popular for rapid weight loss, but the long-term consequences remain the subject of debate. The Scandinavian low-carbohydrate high-fat (LCHF) diet, which has been popular in Scandinavian countries for about a decade, has very low carbohydrate content (~5 E %) but is rich in fat and includes a high proportion of saturated fatty acids. Here we investigated the metabolic and physiological consequences of a diet with a macronutrient composition similar to the Scandinavian LCHF diet and its effects on the organs, tissues, and metabolism of weight stable mice. METHODS: Female C57BL/6J mice were iso-energetically pair-fed for 4 weeks with standard chow or a LCHF diet. We measured body composition using echo MRI and the aerobic capacity before and after 2 and 4 weeks on diet. Cardiac function was assessed by echocardiography before and after 4 weeks on diet. The metabolic rate was measured by indirect calorimetry the fourth week of the diet. Mice were sacrificed after 4 weeks and the organ weight, triglyceride levels, and blood chemistry were analyzed, and the expression of key ketogenic, metabolic, hormonal, and inflammation genes were measured in the heart, liver, and adipose tissue depots of the mice using real-time PCR. RESULTS: The increase in body weight of mice fed a LCHF diet was similar to that in controls. However, while control mice maintained their body composition throughout the study, LCHF mice gained fat mass at the expense of lean mass after 2 weeks. The LCHF diet increased cardiac triglyceride content, impaired cardiac function, and reduced aerobic capacity. It also induced pronounced alterations in gene expression and substrate metabolism, indicating a unique metabolic state. CONCLUSIONS: Pair-fed mice eating LCHF increased their percentage of body fat at the expense of lean mass already after 2 weeks, and after 4 weeks the function of the heart deteriorated. These findings highlight the urgent need to investigate the effects of a LCHF diet on health parameters in humans.

12.
Anticancer Res ; 28(3A): 1493-8, 2008.
Article in English | MEDLINE | ID: mdl-18630503

ABSTRACT

BACKGROUND: Mammaglobin (SCGB2A2) and lipophilin B (SCGB1D2) are members of the secretoglobin polypeptide family. Mammaglobin has been shown to be overexpressed in breast tumor tissue, indicating that mammaglobin might confer a growth advantage to mammaglobin-expressing tumor cells. MATERIALS AND METHODS: The mammaglobin and lipophilin B mRNA expression levels were investigated in seven breast tumors and matched nonneoplastic tissues from the same patients using quantitative real-time RT-PCR. The effect of mammaglobin and lipophilin B expression on breast cancer cell proliferation rates was investigated by analyzing retrovirally transduced Hs578T cell clones. Cell proliferation rates were determined during the exponential growth phase by analyzing the change in lactate dehydrogenase activity over time. RESULTS: All analyzed breast cancer tumors had lower expression levels of mammaglobin and lipophilin B than the respective mean level of the nonneoplastic breast tissues; no prominent overexpression was evident. There was high variability in the expression of mammaglobin and lipophilin B among the non-neoplastic samples, showing that caution should be taken when evaluating their over- and underexpression in tumors. The expression levels of mammaglobin and lipophilin B correlated with each other in the analyzed samples (p = 0.001). Ectopic overexpression of mammaglobin and lipophilin B did not affect the cell proliferation rate of Hs578T breast carcinoma cells in vitro. CONCLUSION: Our findings suggest that the overexpression of mammaglobin observed in certain breast tumors is an epiphenomenon not causally involved in breast carcinogenesis.


Subject(s)
Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Myelin Proteins/biosynthesis , Neoplasm Proteins/biosynthesis , Proteolipids/biosynthesis , Uteroglobin/biosynthesis , Aged , Breast Neoplasms/genetics , Cell Growth Processes/physiology , Cell Lineage , Female , Humans , Mammaglobin A , Middle Aged , Myelin Proteins/genetics , Neoplasm Proteins/genetics , Proteolipids/genetics , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction , Secretoglobins , Transduction, Genetic , Uteroglobin/genetics
13.
Psychiatry Res ; 153(2): 195-8, 2007 Oct 31.
Article in English | MEDLINE | ID: mdl-17659353

ABSTRACT

To examine age at onset of substance abuse in relation to other factors of relevance to criminal behavior, we compared Life History of Aggression (LHA) scores, traits of psychopathy according to the Psychopathy Checklist--Revised (PCL-R), and violent recidivism in 100 violent offenders with early (before the age of 18) versus late onset of abuse or dependence. Of 56 subjects with a history of alcohol and/or drug abuse, an early onset was ascertained in 31. The duration of abuse did not correlate with the LHA and PCL-R scores or with violent recidivism, but the age at onset correlated strongly with all these factors and also remained their strongest correlate in multivariate models including childhood-onset attention deficit/hyperactivity disorder, conduct disorder, and drug abuse as covariates. Strong mathematical associations with aggression, psychopathy, and recidivism pointed to age at onset of substance abuse as a marker of possible complications that require preventive social, educational and medical measures.


Subject(s)
Aggression/psychology , Antisocial Personality Disorder/epidemiology , Crime/statistics & numerical data , Substance-Related Disorders/epidemiology , Adolescent , Age of Onset , Antisocial Personality Disorder/diagnosis , Antisocial Personality Disorder/psychology , Female , Humans , Juvenile Delinquency/statistics & numerical data , Male , ROC Curve , Substance-Related Disorders/diagnosis
14.
Springer Semin Immunopathol ; 28(3): 221-30, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17031650

ABSTRACT

Vaccines have entered into human clinical trials against infectious diseases and as therapies against cancer. The HIV virus establishes a latent infection at a very early stage and the T cell memory of the infected patient is rapidly destroyed. However, results of immunotherapy after DNA and protein immunization show that vaccine-induced immune responses might be present for a long period of time. Patients subjected to therapeutic immunization appear to do well, and to have a small immunological advantage, which, however, will have to be improved. The vaccine therapy should start early, while adequate reservoirs of appropriate T helper cells are available and still inducible. The DNA vaccines induce a relatively long-lived immunological memory, and gene-based immunization is effective in inducing cytotoxic CD8(+) T cells and CD4+ helper cells. Protein vaccines, on the other hand, primarily give T cell help. It thus appears that DNA and protein approaches to HIV immunization complement each other. A surprisingly broad reactivity to peptides from different subtypes of HIV was identified in individuals infected with several subtypes of HIV.


Subject(s)
AIDS Vaccines/therapeutic use , HIV Infections/therapy , T-Lymphocytes/immunology , Vaccines, DNA/therapeutic use , AIDS Vaccines/genetics , AIDS Vaccines/immunology , Adjuvants, Immunologic , Antiretroviral Therapy, Highly Active , CD4-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/immunology , Clinical Trials as Topic , Cytokines/immunology , Cytokines/therapeutic use , HIV Antibodies/biosynthesis , HIV Infections/drug therapy , HIV Infections/immunology , HIV Infections/virology , Humans , Immunologic Memory , Vaccines, DNA/genetics , Vaccines, DNA/immunology , Viral Load
15.
Compr Psychiatry ; 46(2): 111-6, 2005.
Article in English | MEDLINE | ID: mdl-15723027

ABSTRACT

Childhood conduct disorder (CD) and adult psychopathic traits according to the Psychopathy Checklist Revised (PCL-R) were the closest psychiatric covariates to repeated violent crimes and aggression among offenders under forensic psychiatric investigation in Sweden. As psychopathy is not included in the present psychiatric diagnostic systems, we compared total and factor PCL-R scores to Axis I disorders, including childhood-onset neuropsychiatric disorders, and to Axis II personality disorders, to establish the convergence of psychopathic traits with other psychiatric diagnoses, and to identify possible unique features. Psychopathic traits were positively correlated with bipolar mood disorder and negatively with unipolar depression. The total PCL-R scores as well as the Factor 2 (unemotionality) and Factor 3 (behavioral dyscontrol) scores were significantly correlated with attention-deficit/hyperactivity disorder, Asperger's syndrome/high-functioning autistic traits, CD, substance abuse, and the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition Cluster B personality disorders. The interpersonal Factor 1 showed none of these correlations and may capture features that are specific to psychopathy, distinguishing core psychopathy from other diagnostic definitions.


Subject(s)
Antisocial Personality Disorder/epidemiology , Asperger Syndrome/epidemiology , Attention Deficit Disorder with Hyperactivity/epidemiology , Autistic Disorder/epidemiology , Bipolar Disorder/epidemiology , Child Behavior Disorders/epidemiology , Personality Disorders/epidemiology , Adolescent , Adult , Aged , Aggression/psychology , Antisocial Personality Disorder/diagnosis , Antisocial Personality Disorder/psychology , Asperger Syndrome/diagnosis , Asperger Syndrome/psychology , Attention Deficit Disorder with Hyperactivity/diagnosis , Attention Deficit Disorder with Hyperactivity/psychology , Autistic Disorder/diagnosis , Autistic Disorder/psychology , Bipolar Disorder/diagnosis , Bipolar Disorder/psychology , Child , Child Behavior Disorders/diagnosis , Child Behavior Disorders/psychology , Comorbidity , Cross-Sectional Studies , Depressive Disorder/diagnosis , Depressive Disorder/epidemiology , Depressive Disorder/psychology , Female , Humans , Male , Middle Aged , Personality Disorders/diagnosis , Personality Disorders/psychology , Prisoners/psychology , Prisoners/statistics & numerical data , Risk Factors , Sex Offenses/psychology , Sex Offenses/statistics & numerical data , Statistics as Topic , Substance-Related Disorders/diagnosis , Substance-Related Disorders/epidemiology , Substance-Related Disorders/psychology , Violence/psychology , Violence/statistics & numerical data
16.
Acta Neuropathol ; 109(4): 381-6, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15668787

ABSTRACT

Secretoglobins are small secreted proteins, the expression of which has mostly been associated with secretory mucosal epithelia. Several secretoglobins have been implicated in the development of various human cancers. Allelic deletions of chromosome 11q13 correlates with the invasiveness of pituitary tumors. Intriguingly, several secretoglobin genes are located on 11q13; however, for most of these genes the expression in the pituitary and pituitary tumors have not been investigated. Antibodies specific for the secretoglobin lipophilin B (SCGB1D2, BU101) were developed and used in an immunohistochemical analysis of a human normal tissue microarray. Prominent lipophilin B immunoreactivity was found in the secretory cells of the anterior pituitary. Eight of nine analyzed pituitary adenomas showed a reduction in lipophilin B immunoreactivity compared to normal pituitary. However, there was no apparent association between lipophilin B immunoreactivity and hormone production or tumor invasiveness. Expression of eight different secretoglobin mRNAs were analyzed in normal pituitary and the pituitary adenoma cell line HP75 by highly specific quantitative real-time reverse transcription-PCR assays. Lipophilins B and C (SCGB2A1, mammaglobin B) were the most prominently expressed secretoglobin mRNAs in the pituitary. No secretoglobin mRNA was detected in the HP75 cells. The present report demonstrates, for the first time, lipophilin B expression in the pituitary and its apparent down-regulation in pituitary adenomas.


Subject(s)
Adenoma/metabolism , Gene Expression Regulation, Neoplastic/physiology , Myelin Proteins/metabolism , Pituitary Gland/metabolism , Pituitary Neoplasms/metabolism , Proteolipids/metabolism , Blotting, Western/methods , Cell Line, Tumor , Humans , Immunohistochemistry/methods , Mammaglobin B , Myelin Proteins/genetics , Proteolipids/genetics , RNA, Messenger/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction/methods , Secretoglobins , Uteroglobin
17.
Psychiatry Res ; 121(3): 271-80, 2004 Jan 01.
Article in English | MEDLINE | ID: mdl-14675746

ABSTRACT

To describe lifetime mental disorders among perpetrators of severe inter-personal crimes and to identify the problem domains most closely associated with aggression and a history of repeated violent criminality, we used structured interviews, clinical assessments, analyses of intellectual functioning, medical and social files, and collateral interviews in 100 consecutive subjects of pretrial forensic psychiatric investigations. Childhood-onset neuropsychiatric disorders [attention-deficit/hyperactivity disorder (AD/HD), learning disability, tics and autism spectrum disorders] affected 55% of the subjects and formed complex comorbidity patterns with adult personality disorders [including psychopathic traits according to the Psychopathy Checklist (PCL-R)], mood disorders and substance abuse. The closest psychiatric covariates to high Lifetime History of Aggression (LHA) scores and violent recidivism were the PCL-R scores and childhood conduct disorder (CD). Behavioral and affective PCL-R factors were closely associated with childhood AD/HD, CD, and autistic traits. The results support the notion that childhood-onset social and behavioral problems form the most relevant psychiatric symptom cluster in relation to pervasive adult violent behavior, while late-onset mental disorders are more often associated with single acts of violent or sexual aggression.


Subject(s)
Aggression/psychology , Antisocial Personality Disorder/diagnosis , Attention Deficit Disorder with Hyperactivity/diagnosis , Attention Deficit and Disruptive Behavior Disorders/diagnosis , Child Behavior Disorders/diagnosis , Commitment of Mentally Ill/legislation & jurisprudence , Prisoners/psychology , Sex Offenses/psychology , Violence/psychology , Adolescent , Adult , Antisocial Personality Disorder/epidemiology , Antisocial Personality Disorder/psychology , Attention Deficit Disorder with Hyperactivity/epidemiology , Attention Deficit Disorder with Hyperactivity/psychology , Attention Deficit and Disruptive Behavior Disorders/epidemiology , Attention Deficit and Disruptive Behavior Disorders/psychology , Child , Child Behavior Disorders/epidemiology , Child Behavior Disorders/psychology , Comorbidity , Crime/legislation & jurisprudence , Crime/psychology , Expert Testimony/legislation & jurisprudence , Female , Forensic Psychiatry , Humans , Male , Middle Aged , Personality Assessment , Prisoners/statistics & numerical data , Recurrence , Sex Offenses/statistics & numerical data , Violence/legislation & jurisprudence , Violence/statistics & numerical data
19.
Lung Cancer ; 41(1): 49-56, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12826312

ABSTRACT

Lipophilins A, B, C, mammaglobin, and uteroglobin are members of the secretoglobin family of small, secreted, proteins. The functions of these proteins are not well understood but uteroglobin has been implicated in the development of cancers. Uteroglobin is known to be highly expressed in normal lung and down-regulated in lung cancers but expression of the other secretoglobins in normal lung and lung neoplasms have not been investigated. Therefore, we developed quantitative real-time reverse transcription (RT-) PCR assays for the different secretoglobins and evaluated their expression in normal and neoplastic lung tissues. The secretoglobin transcript levels were quantitated by real-time RT-PCR in samples from three normal lungs, 24 lung tumors including six small cell lung carcinomas, seven adenocarcinomas, and five squamous cell carcinomas, and in cell lines from three small cell lung carcinomas and one mesothelioma. Uteroglobin was confirmed to be abundantly expressed in normal lung and the different lung tumors showed down-regulated uteroglobin expression. Of the other secretoglobins, only lipophilin C was detected in normal lung, albeit at low levels. The lung tumors, however, frequently showed neo- or up-regulation of lipophilins A, B, C, and mammaglobin. The results constitute the first quantitative evaluation of secretoglobin expression in normal and neoplastic human lung tissues and demonstrate dysregulation in various human lung cancers. These findings could have important biological and diagnostic implications.


Subject(s)
Carrier Proteins/biosynthesis , Globins/biosynthesis , Lung Neoplasms/metabolism , Lung/metabolism , Myelin Proteins/biosynthesis , Neoplasm Proteins/biosynthesis , Proteolipids/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction/methods , Uteroglobin/biosynthesis , Blotting, Northern , Cell Line, Tumor , DNA, Complementary , Down-Regulation , Humans , Mammaglobin A , Mammaglobin B , RNA, Neoplasm , Secretoglobins , Sensitivity and Specificity , Up-Regulation
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