Searched for: Department/Unit:Cell Biology
Gun Violence and Victimization of Strangers by Persons With a Mental Illness: Data From the MacArthur Violence Risk Assessment Study
Steadman, Henry J; Monahan, John; Pinals, Debra A; Vesselinov, Roumen; Robbins, Pamela Clark
OBJECTIVE: Highly publicized incidents in which people with apparent mental illnesses use guns to victimize strangers have important implications for public views of people with mental illnesses and the formation of mental health and gun policy. The study aimed to provide more data about this topic. METHODS: MacArthur Violence Risk Assessment Study data were analyzed to determine the prevalence of violence by 951 patients after discharge from a psychiatric hospital, including gun violence, violence toward strangers, and gun violence toward strangers. RESULTS: Two percent of patients committed a violent act involving a gun, 6% committed a violent act involving a stranger, and 1% committed a violent act involving both a gun and a stranger. CONCLUSIONS: When public perceptions and policies regarding mental illness are shaped by highly publicized but infrequent instances of gun violence toward strangers, they are unlikely to help people with mental illnesses or to improve public safety.
PMID: 26073414
ISSN: 1557-9700
CID: 2259262
INHIBITION OF MICRORNA-92A PREVENTS ENDOTHELIAL DYSFUNCTION AND ATHEROSCLEROSIS IN MICE [Meeting Abstract]
Loyer, Xavier; Potteaux, Stephane; Vion, Anne-Clemence; Guerin, Coralie L; Boulkroun, Sheerazade; Rautou, Pierre-Emmanule; Ramkhelawon, Bhama; Esposito, Bruno; Dalloz, Marion; Paul, Jean-Louis; Julia, Pierre; Maccario, Jean; Boulanger, Chantal M; Mallat, Ziad; Tedgui, Alain
ISI:000355975600011
ISSN: 1423-0135
CID: 2245312
Gut microbiome in early pediatric MS : a case-control study [Meeting Abstract]
Tremlett, H; Fadrosh, D; Lynch, S; Hart, J; Graves, J; Lulu, S; Aaen, G; Belman, Anita; Benson, L; Casper, C; Chitnis, T; Gorman, M; Krupp, Lauren; Lotze, T; Ness, J; Roalstad, S; Rodriguez, M; Rose, J; Mendelt-Tilleman, J; Weinstock-Guttman, B; Waubant, E
ORIGINAL:0011420
ISSN: 1526-632x
CID: 2236632
HOW MANY CARRIERS ARE YOU MISSING?: THE VALUE OF EXPANDED CARRIER SCREENING [Meeting Abstract]
Yarnall, S; Bristow, SL; Kellogg, GR; Kumar, N; Rodriguez, S; Shraga, R; Gold, M; Noyes, N; Keefe, DL
ISI:000380018900168
ISSN: 1556-5653
CID: 2220002
TELOMERE ATTRITION IN GERMINAL VESICLE ARRESTED HUMAN OOCYTES. [Meeting Abstract]
Kalmbach, K; Keefe, DL
ISI:000380018900532
ISSN: 1556-5653
CID: 2220362
INHIBITION OF THE PI3K/AKT/MTOR PATHWAY IN A MURINE MODEL ATTENUATES PRIMORDIAL FOLLICLE DEPLETION DURING GONADOTOXIC CHEMOTHERAPY. [Meeting Abstract]
Goldman, KN; Keefe, DL; Arju, R; Duncan, FE; Grifo, J; Schneider, R
ISI:000380018900678
ISSN: 1556-5653
CID: 2220062
OVARIAN RESERVE AND RESPONSE ARE ASSOCIATED WITH OOCYTE TELOMERE DNA CONTENT NOT PERIPHERAL BLOOD TELOMERE DNA CONTENT. [Meeting Abstract]
Kalmbach, K; Antunes, DM; Kramer, YG; McCulloh, DH; Keefe, DL
ISI:000380018900531
ISSN: 1556-5653
CID: 2220052
Pharmacokinetics, Safety, and Tolerability of a Single 500-mg or 1000-mg Intravenous Dose of Dalbavancin in Healthy Japanese Subjects
Scoble, Patrick J; Owens, Robert C Jr; Puttagunta, Sailaja; Yen, Mark; Dunne, Michael W
BACKGROUND AND OBJECTIVES: Dalbavancin is a novel, once-weekly glycopeptide antibiotic approved for treatment of acute bacterial skin infections. Given the importance of understanding any pharmacokinetic variability across different patient populations, a double-blind, placebo-controlled study was conducted to evaluate the pharmacokinetics, safety, and tolerability of a single 500-mg and a single 1000-mg intravenous dose of dalbavancin in healthy Japanese subjects. METHODS: Ten subjects received intravenous dalbavancin 1000 mg, five subjects received intravenous dalbavancin 500 mg, and three subjects received intravenous placebo. RESULTS: After a single infusion of dalbavancin, the maximal plasma concentration (C max) and area under the plasma concentration-time curve (AUC) increased in a proportional manner from 500 mg to 1000 mg (C max: 157 mug/ml and 299 mug/ml; AUClast: 10,850 mug.h/ml and 22,679 mug.h/ml, on the 500-mg and 1000-mg regimens, respectively) with low inter-subject variability. The mean terminal phase half-life (t 1/2) was 204 and 193 h after the 500-mg and 1000-mg dose, respectively. Clearance and volume of distribution were similar for the two dose concentrations. Treatment-emergent adverse events reported were considered to be of mild intensity. There were no relevant changes in laboratory values or vital signs over time in subjects in either treatment group. CONCLUSIONS: Overall, dalbavancin 500 mg and dalbavancin 1000 mg, administered as a single 30-min infusion, was well tolerated in this population and resulted in plasma exposures similar to those in non-Asians.
PMCID:4659844
PMID: 26458939
ISSN: 1179-1918
CID: 2216492
In Vitro Activity of Dalbavancin against Drug-Resistant Staphylococcus aureus Isolates from a Global Surveillance Program
McCurdy, Sandra P; Jones, Ronald N; Mendes, Rodrigo E; Puttagunta, Sailaja; Dunne, Michael W
In over a decade (2002 to 2012) of Staphylococcus aureus surveillance testing on 62,195 isolates, dalbavancin was demonstrated to be active against isolates that were either susceptible or nonsusceptible to daptomycin, linezolid, or tigecycline. Nearly all (99.8%) multidrug-resistant methicillin-resistant S. aureus isolates were inhibited by dalbavancin at =0.12 mug/ml (MIC50/90, 0.06/0.06 mug/ml), the current U.S. Food and Drug Administration (U.S. FDA) breakpoint. Overall, only 0.35% of the monitored S. aureus isolates had a dalbavancin MIC of either 0.25 or 0.5 mug/ml (i.e., were nonsusceptible).
PMCID:4505194
PMID: 25987636
ISSN: 1098-6596
CID: 2216502
Extended-duration dosing and distribution of dalbavancin into bone and articular tissue
Dunne, Michael W; Puttagunta, Sailaja; Sprenger, Craig R; Rubino, Chris; Van Wart, Scott; Baldassarre, James
Dalbavancin is an intravenous lipoglycopeptide with activity against Gram-positive pathogens and an MIC90 for Staphylococcus aureus of 0.06 mug/ml. With a terminal half-life of >14 days, dosing regimens with infrequent parenteral administration become available to treat infectious diseases such as osteomyelitis and endocarditis that otherwise require daily dosing for many weeks. In order to support a rationale for these novel regimens, the pharmacokinetics over an extended dosing interval and the distribution of dalbavancin into bone and articular tissue were studied in two phase I trials and pharmacokinetic modeling was performed. Intravenous administration of 1,000 mg of dalbavancin on day 1 followed by 500 mg weekly for seven additional weeks was well tolerated and did not demonstrate evidence of drug accumulation. In a separate study, dalbavancin concentrations in cortical bone 12 h after infusion of a single 1,000-mg intravenous infusion were 6.3 mug/g and 2 weeks later were 4.1 mug/g. A two-dose, once-weekly regimen that would provide tissue exposure over the dalbavancin MIC for Staphylococcus aureus for 8 weeks, maximizing the initial exposure to treatment while minimizing the frequency of intravenous therapy, is proposed.
PMCID:4356775
PMID: 25561338
ISSN: 1098-6596
CID: 2216522