Star Formation in the Radio Galaxy NGC 4410A

The NGC4410 group of galaxies provides us a rare opportunity to study a nearby (97 h75^-1 Mpc) example of a radio galaxy (NGC4410A) embedded in an extended X-ray source, with evidence for star formation that can be readily spatially distinguished from regions dominated by the AGN and shocks. We present broadband and narrowband optical images along with optical and IUE ultraviolet spectroscopy for the radio galaxy NGC 4410A and its companion NGC 4410B. Our H-alpha+[NII] images reveal six luminous HII regions (L_H-alpha ~ 1e40 erg/s distributed in an arc near NGC 4410A. Partially completing the ring is a prominent stellar loop containing diffuse ionized gas. This filamentary gas, in contrast to the H II regions, shows spectroscopic signatures of shock ionization. The star formation in this system may have been triggered by a collision or interaction between the two galaxies, perhaps by an expanding density wave, as in classical models of ring galaxies. Alternatively, the star formation may have been induced by the impact of a radio jet on the interstellar matter. Extended Ly-alpha is detected in the ultraviolet IUE spectrum. The ultraviolet continuum, which is presumably radiated by the nucleus of NGC4410A, is not extended. NGC4410A appears to be interacting with its neighbors in the NGC4410 group, and could be an example of a spiral galaxy transforming into an elliptical.Comment: 33 pages, 9 figures. Accepted for publication in April, 2002 A

A Study of 3CR Radio Galaxies from z = 0.15 to 0.65. II. Evidence for an Evolving Radio Structure

Radio structure parameters were measured from the highest quality radio maps available for a sample of 3CR radio galaxies in the redshift range 0.15 < z < 0.65. Combined with similar data for quasars in the same redshift range, these morphology data are used in conjunction with a quantification of the richness of the cluster environment around these objects (the amplitude of the galaxy-galaxy spatial covariance function, Bgg) to search for indirect evidence of a dense intracluster medium (ICM). This is done by searching for confinement and distortions of the radio structure that are correlated with Bgg. Correlations between physical size and hot spot placement with Bgg show evidence for an ICM only at z 0.4, suggesting an epoch of z ~ 0.4 for the formation of an ICM in these Abell richness class 0-1, FR2-selected clusters. X-ray selected clusters at comparable redshifts, which contain FR1 type sources exclusively, are demonstrably richer than the FR2-selected clusters found in this study. The majority of the radio sources with high Bgg values at z < 0.4 can be described as ``fat doubles'' or intermediate FR2/FR1s. The lack of correlation between Bgg and bending angle or Bgg and lobe length asymmetry suggests that these types of radio source distortion are caused by something other than interaction with a dense ICM. Thus, a large bending angle cannot be used as an unambiguous indicator of a rich cluster around powerful radio sources. These results support the hypothesis made in Paper 1 that cluster quasars fade to become FR2s, then FR1s, on a timescale of 0.9 Gyrs (for H0 = 50 km s^-1 Mpc^-1).Comment: 44 pages, 8 figures, 2 tables; to be published in the September 2002 issue of The Astronomical Journa

Consumer Socialization and the Role of Branding in Hazardous Adolescent Drinking

This study examines the relationship between alcohol marketing and consumer socialization to alcohol brands (assessed here using aided and unaided brand recognition and brand saliency), and the associated relationship between consumer socialization and hazardous alcohol consumption among a cohort of adolescents surveyed in Scotland. The research addresses gaps in the consumer socialization literature, by examining how marketing influences brand consumer socialization, and how brand consumer socialization influences subsequent hazardous consumption behavior over time, using a robust longitudinal design that assesses causal relationships while controlling for a wide range of important confounding variables. The results demonstrate the contribution of marketing to adolescents’ brand socialization to alcohol and the impact of this socialization on subsequent drinking behaviors. Implications for marketing managers, parents, policymakers, and consumer researchers are discussed, together with suggestions for future consumer research

Diagnostic criteria for oncocytic renal neoplasms:a survey of urologic pathologists

Renal oncocytoma and chromophobe renal cell carcinoma (RCC) have been long recognized as distinct tumors; however, it remains unknown if uniform diagnostic criteria are used to distinguish these tumor types in practice. A survey was distributed to urologic pathologists regarding oncocytic tumors. Responses were received from 17/26 invitees. Histologically, >1 mitotic figure was regarded as most worrisome (n=10) or incompatible (n=6) with oncocytoma diagnosis. Interpretation of focal nuclear wrinkling, focal perinuclear clearing, and multinucleation depended on extent and did not necessarily exclude oncocytoma if minor. Staining techniques most commonly used included: CK7 (94%), KIT (71%), vimentin (65%), colloidal iron (59%), CD10 (53%), and AMACR (41%). Rare CK7-positive cells (≤5%) was regarded as most supportive of oncocytoma, although an extent excluding oncocytoma was not universal. Multiple chromosomal losses were most strongly supportive for chromophobe RCC diagnosis (65%). Less certainty was reported for chromosomal gain or a single loss. For tumors with mixed or inconclusive features, many participants use an intermediate diagnostic category (82%) that does not label the tumor as unequivocally benign or malignant, typically "oncocytic neoplasm" or "tumor" with comment. The term "hybrid tumor" was used variably in several scenarios. A slight majority (65%) report outright diagnosis of oncocytoma in needle biopsies. The morphologic, immunohistochemical, and genetic characteristics that define oncocytic renal tumors remain incompletely understood. Further studies correlating genetics, behavior, and histology are needed to define which tumors truly warrant classification as carcinomas for patient counseling and follow-up strategies

Recurrent Coding Sequence Variation Explains only A Small Fraction of the Genetic Architecture of Colorectal Cancer

Whilst common genetic variation in many non-coding genomic regulatory regions are known to impart risk of colorectal cancer (CRC), much of the heritability of CRC remains unexplained. To examine the role of recurrent coding sequence variation in CRC aetiology, we genotyped 12,638 CRCs cases and 29,045 controls from six European populations. Single-variant analysis identified a coding variant (rs3184504) in SH2B3 (12q24) associated with CRC risk (OR = 1.08, P = 3.9 × 10-7), and novel damaging coding variants in 3 genes previously tagged by GWAS efforts; rs16888728 (8q24) in UTP23 (OR = 1.15, P = 1.4 × 10-7); rs6580742 and rs12303082 (12q13) in FAM186A (OR = 1.11, P = 1.2 × 10-

Development and Validation of a Risk Score for Chronic Kidney Disease in HIV Infection Using Prospective Cohort Data from the D:A:D Study

Ristola M. on työryhmien DAD Study Grp ; Royal Free Hosp Clin Cohort ; INSIGHT Study Grp ; SMART Study Grp ; ESPRIT Study Grp jäsen.Background Chronic kidney disease (CKD) is a major health issue for HIV-positive individuals, associated with increased morbidity and mortality. Development and implementation of a risk score model for CKD would allow comparison of the risks and benefits of adding potentially nephrotoxic antiretrovirals to a treatment regimen and would identify those at greatest risk of CKD. The aims of this study were to develop a simple, externally validated, and widely applicable long-term risk score model for CKD in HIV-positive individuals that can guide decision making in clinical practice. Methods and Findings A total of 17,954 HIV-positive individuals from the Data Collection on Adverse Events of Anti-HIV Drugs (D:A:D) study with >= 3 estimated glomerular filtration rate (eGFR) values after 1 January 2004 were included. Baseline was defined as the first eGFR > 60 ml/min/1.73 m2 after 1 January 2004; individuals with exposure to tenofovir, atazanavir, atazanavir/ritonavir, lopinavir/ritonavir, other boosted protease inhibitors before baseline were excluded. CKD was defined as confirmed (>3 mo apart) eGFR In the D:A:D study, 641 individuals developed CKD during 103,185 person-years of follow-up (PYFU; incidence 6.2/1,000 PYFU, 95% CI 5.7-6.7; median follow-up 6.1 y, range 0.3-9.1 y). Older age, intravenous drug use, hepatitis C coinfection, lower baseline eGFR, female gender, lower CD4 count nadir, hypertension, diabetes, and cardiovascular disease (CVD) predicted CKD. The adjusted incidence rate ratios of these nine categorical variables were scaled and summed to create the risk score. The median risk score at baseline was -2 (interquartile range -4 to 2). There was a 1: 393 chance of developing CKD in the next 5 y in the low risk group (risk score = 5, 505 events), respectively. Number needed to harm (NNTH) at 5 y when starting unboosted atazanavir or lopinavir/ritonavir among those with a low risk score was 1,702 (95% CI 1,166-3,367); NNTH was 202 (95% CI 159-278) and 21 (95% CI 19-23), respectively, for those with a medium and high risk score. NNTH was 739 (95% CI 506-1462), 88 (95% CI 69-121), and 9 (95% CI 8-10) for those with a low, medium, and high risk score, respectively, starting tenofovir, atazanavir/ritonavir, or another boosted protease inhibitor. The Royal Free Hospital Clinic Cohort included 2,548 individuals, of whom 94 individuals developed CKD (3.7%) during 18,376 PYFU (median follow-up 7.4 y, range 0.3-12.7 y). Of 2,013 individuals included from the SMART/ESPRIT control arms, 32 individuals developed CKD (1.6%) during 8,452 PYFU (median follow-up 4.1 y, range 0.6-8.1 y). External validation showed that the risk score predicted well in these cohorts. Limitations of this study included limited data on race and no information on proteinuria. Conclusions Both traditional and HIV-related risk factors were predictive of CKD. These factors were used to develop a risk score for CKD in HIV infection, externally validated, that has direct clinical relevance for patients and clinicians to weigh the benefits of certain antiretrovirals against the risk of CKD and to identify those at greatest risk of CKD.Peer reviewe

Collecting duct carcinoma versus renal medullary carcinoma: An appeal for nosologic and biological clarity

Editorial (No abstract available