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Rasagiline, Parkinson neuroprotection, and delayed-start trials
Ahlskog, J. Eric , Uitti, Ryan J.

Neurology | April 5, 2010 | Volume: 74 | Issue: 14 | Pages: 1143-1148

10.1212/wnl.0b013e3181d7d8e2 | PMID 20368634 Get It

Upregulation of DNA Methyltransferase–Mediated Gene Silencing, Anchorage-Independent Growth, and Migration of Colon Cancer Cells by Interleukin-6
Foran, Eílis, Garrity-Park, Megan, Mureau, Coralie, Newell, John , Smyrk, Thomas C. , Egan, Laurence J. , Limburg, Paul J.

Molecular Cancer Research | March 31, 2010 | Volume: 8 | Issue: 4 | Pages: 471-481

10.1158/1541-7786.mcr-09-0496 | PMID 20354000 Get It

Abstract Inflammatory bowel disease is characterized by chronic inflammation which predisposes to colorectal cancer. The mechanisms by which inflammation promotes tumorigenesis are not fully known. We aimed to investigate the links between colonic inflammation and tumorigenesis via epigenetic gene silencing. Colon cancer specimens were assessed for the expression of DNA methyltransferase-1 (DNMT-1) using immunohistochemistry. Colorectal carcinoma cell lines were assessed for DNMT1 expression, methylcytosine content, promoter methylation, gene expression, and tumorigenesis in response to interleukin (IL)-6. DNMT1 was expressed at higher levels in both the peritumoral stroma and tumor in inflammatory bowel disease–associated cancers compared with sporadic colon cancers. IL-6 treatment of colon cancer cells resulted in an increase in DNMT1 expression, independent of de novo gene expression. IL-6 increased the methylation of promoter regions of genes associated with tumor suppression, adhesion, and apoptosis resistance. Expression of a subset of these genes was downregulated by IL-6, an effect that was prevented by preincubation with 5-azadeoxycytidine, a DNMT1 inhibitor. Anchorage-independent growth and migration of colon cancer cells was also increased by IL-6 in a 5-azadeoxycytidine–sensitive manner. Our results indicate that DNMT-mediated gene silencing may play a role in inflammation-associated colon tumorigenesis. Mol Cancer Res; 8(4); 471–81. ©2010 AACR.
Automated Prone Positioning and Axial Rotation in Critically Ill, Nontrauma Patients With Acute Respiratory Distress Syndrome (ARDS)
Arasi, Lisa C., Canabal, Juan, Kramer, David J., Bajwa, Abubakr A.

Journal of Intensive Care Medicine | March 25, 2010 | Volume: 25 | Issue: 2 | Pages: 121-125

10.1177/0885066609356050 | PMID 20338893 Get It

The Physics of Clinical MR Taught Through Images, 2nd ed.
Smith, Michael Brent

American Journal of Roentgenology | March 22, 2010 | Volume: 194 | Issue: 4 | Pages: W347-W347

10.2214/ajr.09.3190 Get It

Ulcerative colitis, infliximab, and hepatic epithelioid hemangioendothelioma: who is to blame? Case Report
Chang, Joseph , Marks, Randolph S., Nagorney, David M. , Sanderson, Schuyler O., Kane, Sunanda V.

Therapeutic Advances in Gastroenterology | March 19, 2010 | Volume: 3 | Issue: 3 | Pages: 203-206

10.1177/1756283x10363015 | PMID 21180602 Get It

The International LAM Registry: A Component of an Innovative Web-Based Clinician, Researcher, and Patient-Driven Rare Disease Research Platform
Nurok, Michael , Eslick, Ian , Carvalho, Carlos Roberto Ribeiro de , Costabel, Ulrich , Glanville, Allan R. , Harari, Sergio , Johnson, Simon R. , Lacronique, J, Lazor, Romain , Moss, Joel , Ruoss, Stephen J. , Ryu, Jay H. , Seyama, Kuniaki , Watz, Henrik, Hohmann, Elizabeth , Moss, Frank, D'Armiento, Jeanine M , Henske, Elizabeth P. , Inoue, Yoshikazu , Xu, Kai‐Feng , Ryu, Jay H

Lymphatic Research and Biology | March 17, 2010 | Volume: 8 | Issue: 1 | Pages: 81-87

10.1089/lrb.2009.0028 | PMID 20235890 Get It

OnabotulinumtoxinA for treatment of chronic migraine: Results from the double-blind, randomized, placebo-controlled phase of the PREEMPT 2 trial
Diener, HC, Dodick, DW, Aurora, SK, Turkel, CC, DeGryse, RE, Lipton, RB, Silberstein, SD, Brin, MF

Cephalalgia | March 17, 2010 | Volume: 30 | Issue: 7 | Pages: 804-814

10.1177/0333102410364677 | PMID 20647171 Get It

Objectives: This is the second of a pair of studies designed to evaluate the efficacy and safety of onabotulinumtoxinA (BOTOX®) for prophylaxis of headaches in adults with chronic migraine. Methods: PREEMPT 2 was a phase 3 study, with a 24-week, double-blind, placebo-controlled phase, followed by a 32-week, open-label phase. Subjects were randomized (1:1) to injections of onabotulinumtoxinA (155U–195U; n = 347) or placebo ( n = 358) every 12 weeks for two cycles. The primary efficacy endpoint was mean change in headache days per 28 days from baseline to weeks 21–24 post-treatment. Results: OnabotulinumtoxinA was statistically significantly superior to placebo for the primary endpoint, frequency of headache days per 28 days relative to baseline (−9.0 onabotulinumtoxinA/−6.7 placebo, p < .001). OnabotulinumtoxinA was significantly favoured in all secondary endpoint comparisons. OnabotulinumtoxinA was safe and well tolerated, with few treatment-related adverse events. Few patients (3.5% onabotulinumtoxinA/1.4% placebo) discontinued due to adverse events. Conclusions: The results of PREEMPT 2 demonstrate that onabotulinumtoxinA is effective for prophylaxis of headache in adults with chronic migraine. Repeated onabotulinumtoxinA treatments were safe and well tolerated.
OnabotulinumtoxinA for treatment of chronic migraine: Results from the double-blind, randomized, placebo-controlled phase of the PREEMPT 1 trial
Aurora, SK, Dodick, DW, Turkel, CC, DeGryse, RE, Silberstein, SD, Lipton, RB, Diener, HC, Brin, MF, Dashtipour, Khashayar

Cephalalgia | March 17, 2010 | Volume: 30 | Issue: 7 | Pages: 793-803

10.1177/0333102410364676 | PMID 20647170 Get It

Objectives: This is the first of a pair of studies designed to assess efficacy, safety and tolerability of onabotulinumtoxinA (BOTOX®) as headache prophylaxis in adults with chronic migraine. Methods: The Phase III REsearch Evaluating Migraine Prophylaxis Therapy 1 (PREEMPT 1) is a phase 3 study, with a 24-week, double-blind, parallel-group, placebo-controlled phase followed by a 32-week, open-label phase. Subjects were randomized (1:1) to injections every 12 weeks of onabotulinumtoxinA (155 U–195 U; n = 341) or placebo ( n = 338) (two cycles). The primary endpoint was mean change from baseline in headache episode frequency at week 24. Results: No significant between-group difference for onabotulinumtoxinA versus placebo was observed for the primary endpoint, headache episodes (−5.2 vs. −5.3; p = 0.344). Large within-group decreases from baseline were observed for all efficacy variables. Significant between-group differences for onabotulinumtoxinA were observed for the secondary endpoints, headache days ( p = .006) and migraine days ( p = 0.002). OnabotulinumtoxinA was safe and well tolerated, with few treatment-related adverse events. Few subjects discontinued due to adverse events. Conclusions: There was no between-group difference for the primary endpoint, headache episodes. However, significant reductions from baseline were observed for onabotulinumtoxinA for headache and migraine days, cumulative hours of headache on headache days and frequency of moderate/severe headache days, which in turn reduced the burden of illness in adults with disabling chronic migraine.
Conference Scene: The Great Debate: Genome-Wide Association Studies in Pharmacogenetics Research, Good or Bad?
Bailey, Kent R. , Cheng, Cheng

Pharmacogenomics | March 17, 2010 | Volume: 11 | Issue: 3 | Pages: 305-308

10.2217/pgs.10.6 | PMID 20235786 Get It

Hockey Education Program (HEP): A Statewide Measure of Fair Play, Skill Development, and Coaching Excellence
Smith, Aynsley M., Jorgenson, M. B., Sorenson, Matthew C., Margenau, David, Link, Andrew A., MacMillan, Michael, Stuart, Michael J.

Fifth International Symposium on Safety in Ice Hockey | March 15, 2010 | Volume: No volume available | Issue: No issue available | Pages: 291-310

10.1520/stp48878s Get It

Following the death of a youth hockey coach in a fight with a parent in 2000, the Mayo Clinic Sports Medicine Center and Minnesota Hockey collaborated to implement a three-component Hockey Education Program (HEP). HEP was initiated in 2003 to ensure youth players develop sportsmanship, skills, and a Fair Play approach to the game. Another goal was to decrease attrition of players, coaches, and officials. Coaching Excellence, a component of HEP, is based on 25 years of youth sport research. The HEP manuals Coaches Who Never Lose and Sports and Your Child contain the philosophy, objectives, and guidelines to ensure implementation of HEP components across players, coaches, and parents. The Skill Development component emphasizes learning age-appropriate hockey skills though skill progression. Increasing the practice-to-game ratio to 3–4 practices per game greatly increases the maximum time players skate with the puck during developmental years. Pre- and post-season Skills Challenges allow coaches, players, and parents to gauge improvement, and structure practices to address identified skill deficits. The Fair Play (FP) component emphasizes sportsmanship. Teams earn a FP point each game if they incur less than a preset number of penalty minutes. A coach receiving a game misconduct or a parent∕spectator asked to leave the game will cause the team to forfeit their FP point. FP points are factored into league standings across the state. This past season, 17 678 records of game data were obtained and 25 % (4420) were randomly selected for analysis. The data analysis permits comparison across seasons and changes are made accordingly. Based on four years of data, most Minnesota youth hockey games are played in a sportsmanlike manner. Checking from behind and head contact penalties have decreased since the penalty minutes for these dangerous infractions were increased.