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ERBB Receptor Activation Is Required for Profibrotic Responses to Transforming Growth Factor β
Andrianifahanana, Mahefatiana, Wilkes, Mark C. , Repellin, Claire E. , Edens, Maryanne, Rahimi, Rod A. , Leof, Edward B. , Kottom, Theodore J.

Cancer Research | September 14, 2010 | Volume: 70 | Issue: 19 | Pages: 7421-7430

10.1158/0008-5472.can-10-0232 | PMID 20841477 Get It

Abstract Engagement of the transforming growth factor-β (TGF-β) receptor complex activates multiple signaling pathways that play crucial roles in both health and disease. TGF-β is a key regulator of fibrogenesis and cancer-associated desmoplasia; however, its exact mode of action in these pathologic processes has remained poorly defined. Here, we report a novel mechanism whereby signaling via members of the ERBB or epidermal growth factor family of receptors serves as a central requirement for the biological responses of fibroblasts to TGF-β. We show that TGF-β triggers upregulation of ERBB ligands and activation of cognate receptors via the canonical SMAD pathway in fibroblasts. Interestingly, activation of ERBB is commonly observed in a subset of fibroblast but not epithelial cells from different species, indicating cell type specificity. Moreover, using genetic and pharmacologic approaches, we show that ERBB activation by TGF-β is essential for the induction of fibroblast cell morphologic transformation and anchorage-independent growth. Together, these results uncover important aspects of TGF-β signaling that highlight the role of ERBB ligands/receptors as critical mediators in fibroblast responses to this pleiotropic cytokine. Cancer Res; 70(19); 7421–30. ©2010 AACR.
Erratum to: Surgical treatment of peroneal nerve palsy after knee dislocation
Giuseffi, Steven A., Shin, Alexander Y. , Dahm, Diane L., Levy, Bruce A. , Bishop, Allen T. , Stuart, Michael J. , Shin, Alexander Y

Knee Surgery, Sports Traumatology, Arthroscopy | September 14, 2010 | Volume: 18 | Issue: 11 | Pages: 1626-1626

10.1007/s00167-010-1261-7 Get It

Stimulant-Responsive and Stimulant-Refractory Aggressive Behavior Among Children With ADHD
Blader, Joseph C. , Pliszka, Steven R. , Jensen, Peter S. , Schooler, Nina R. , Kafantaris, Vivian

Pediatrics | September 13, 2010 | Volume: 126 | Issue: 4 | Pages: e796-e806

10.1542/peds.2010-0086 | PMID 20837589 Get It

OBJECTIVES: The objective of this study was to examine factors that are associated with aggression that is responsive versus refractory to individualized optimization of stimulant monotherapy among children with attention-deficit/hyperactivity disorder (ADHD). METHODS: Children who were aged 6 to 13 years and had ADHD, either oppositional defiant disorder or conduct disorder, significant aggressive behavior, and a history of insufficient response to stimulants completed an open stimulant monotherapy optimization protocol. Stimulant titration with weekly assessments of behavior and tolerability identified an optimal regimen for each child. Families also received behavioral therapy. Parents completed the Retrospective-Modified Overt Aggression Scale (R-MOAS) at each visit. Children were classified as having stimulant-refractory aggression on the basis of R-MOAS ratings and clinician judgment. Differences that pertained to treatment, demographic, and psychopathology between groups with stimulant monotherapy–responsive and –refractory aggression were evaluated. RESULTS: Aggression among 32 (49.3%) of 65 children was reduced sufficiently after stimulant dosage adjustment and behavioral therapy to preclude adjunctive medication. Those who responded to stimulant monotherapy were more likely to benefit from the protocol's methylphenidate preparation (once-daily, triphasic release), showed a trend for lower average dosages, and received fewer behavioral therapy sessions than did children with stimulant-refractory aggression. Boys, especially those with higher ratings of baseline aggression and of depressive and manic symptoms, more often exhibited stimulant-refractory aggression. CONCLUSIONS: Among children whose aggressive behavior develops in the context of ADHD and of oppositional defiant disorder or conduct disorder, and who had insufficient response to previous stimulant treatment in routine clinical care, systematic, well-monitored titration of stimulant monotherapy often culminates in reduced aggression that averts the need for additional agents.
Late Outcomes of Reintervention on the Descending Aorta After Repair of Aortic Coarctation
Brown, Morgan L. , Burkhart, Harold M. , Connolly, Heidi M. , Hagler, Donald J. , Schaff, Hartzell V. , Dearani, Joseph A. , Schaff, Hartzell

Circulation | September 13, 2010 | Volume: 122 | Issue: 11_suppl_1 | Pages: No page available

10.1161/circulationaha.109.925172 | PMID 20837930 Get It

Background— After repair of aortic coarctation, patients may develop restenosis, aneurysms, and pseudoaneurysms at the site of prior repair. We assessed the outcomes of late reintervention on the descending aorta after aortic coarctation repair. Methods and Results— From March 1954 to July 2008, 130 patients had operations or endovascular procedures on the descending aorta after previous coarctation repair. We excluded patients who had complex left-sided cardiac lesions or interrupted aortic arch. Mean age at reintervention was 32±24 years and 28% were female. The interval between coarctation repair and reintervention was 17±13 years. Seventy-four percent of patients had hypertension. Reasons for reintervention were restenosis (n=122 [94%]), aneurysm (n=4 [3%]), and pseudoaneurysm (n=4 [3%]). Ninety-five patients (73%) underwent operative procedures including an extra-anatomic conduit (n=41), patch repair (n=32), interposition graft (n=14), end–end anastomosis (n=6), and subclavian flap (n=2). Thirty-five patients underwent endovascular treatment (balloon dilatation, n=22 or stenting, n=13). There was no early mortality. In the surgical group, 5 patients required early reoperation for bleeding and 5 patients had early vocal cord paralysis. One patient in the endovascular group had aortic rupture at the time of intervention requiring urgent operation. Survival was 97% at 10 years. At 5 years, freedom from a second repeat procedure on the descending aorta was 96% in the surgical group and 72% in the endovascular group ( P <0.001). Five years after reintervention, fewer patients required treatment for hypertension (57% versus 74% , P <0.001) and a median of 1 antihypertensive medication was prescribed compared with a median of 2 medications preintervention. Conclusions— Operative and endovascular management of recoarctation can be performed safely with good late outcomes.
Five-Year Follow-Up of a Randomized Comparison Between Off-Pump and On-Pump Stable Multivessel Coronary Artery Bypass Grafting. The MASS III Trial
Hueb, Whady , Lopes, Neuza , Pereira, Alexandre C. , Hueb, Alexandre Ciappina , Soares, Paulo Rogério , Favarato, Desidério , Vieira, Ricardo D’Oliveira , Paulitch, Felipe da Silva, César, Luı́z Antonio Machado , Ramires, José Antônio Franchini , Lima, Eduardo Gomes , Garzillo, Cibele Larrosa , Gersh, Bernard J.

Circulation | September 13, 2010 | Volume: 122 | Issue: 11_suppl_1 | Pages: No page available

10.1161/circulationaha.109.924258 | PMID 20837925 Get It

Background— Coronary artery bypass graft surgery with cardiopulmonary bypass is a safe, routine procedure. Nevertheless, significant morbidity remains, mostly because of the body’s response to the nonphysiological nature of cardiopulmonary bypass. Few data are available on the effects of off-pump coronary artery bypass graft surgery (OPCAB) on cardiac events and long-term clinical outcomes. Methods and Results— In a single-center randomized trial, 308 patients undergoing coronary artery bypass graft surgery were randomly assigned: 155 to OPCAB and 153 to on-pump CAB (ONCAB). Primary composite end points were death, myocardial infarction, further revascularization (surgery or angioplasty), or stroke. After 5-year follow-up, the primary composite end point was not different between groups (hazard ratio 0.71, 95% CI 0.41 to 1.22; P =0.21). A statistical difference was found between OPCAB and ONCAB groups in the duration of surgery (240±65 versus 300±87.5 minutes; P <0.001), in the length of ICU stay (19.5±17.8 versus 43±17.0 hours; P <0.001), time to extubation (4.6±6.8 versus 9.3±5.7 hours; P <0.001), hospital stay (6±2 versus 9±2 days; P <0.001), higher incidence of atrial fibrillation (35 versus 4% of patients; P <0.001), and blood requirements (31 versus 61% of patients; P <0.001), respectively. The number of grafts per patient was higher in the ONCAB than the OPCAB group (2.97 versus 2.49 grafts/patient; P <0.001). Conclusions— No difference was found between groups in the primary composite end point at 5-years follow-up. Although OPCAB surgery was related to a lower number of grafts and higher episodes of atrial fibrillation, it had no significant implications related to long-term outcomes. Clinical Trial Registration— URL: http://www.controlled-trials.com. Unique identifier: ISRCTN66068876.
International Society for Sexual Medicine’s Guidelines for the Diagnosis and Treatment of Premature Ejaculation
Althof, Stanley E., Abdo, Carmita Helena Najjar , Dean, John, Hackett, Geoff , McCabe, Marita P. , McMahon, Chris G., Rosen, Raymond C., Sadovsky, Richard, Waldinger, Marcel D., Becher, Edgardo, Broderick, Gregory A. , Buvat, Jacques, El-Meliegy, Amr, Hellstrom, Wayne J.G. , Incrocci, Luca , Jannini, Emmanuele A. , Park, Kwangsung , Parish, Sharon J. , Porst, Hartmut, Segraves, Robert, Sharlip, Ira D., Simonelli, Chiara , Tan, Hui Meng, Buvat, Jacques, Goldstein, Irwin , Giuliano, François , Rowland, David L.

The Journal of Sexual Medicine | September 13, 2010 | Volume: 7 | Issue: 9 | Pages: 2947-2969

10.1111/j.1743-6109.2010.01975.x | PMID 21050394 Get It

ABSTRACTIntroductionOver the past 20 years our knowledge of premature ejaculation (PE) has significantly advanced. Specifically, we have witnessed substantial progress in understanding the physiology of ejaculation, clarifying the real prevalence of PE in population-based studies, reconceptualizing the definition and diagnostic criterion of the disorder, assessing the psychosocial impact on patients and partners, designing validated diagnostic and outcome measures, proposing new pharmacologic strategies and examining the efficacy, safety and satisfaction of these new and established therapies. Given the abundance of high level research it seemed like an opportune time for the International Society for Sexual Medicine (ISSM) to promulgate an evidenced-based, comprehensive and practical set of clinical guidelines for the diagnosis and treatment of PE.AimDevelop clearly worded, practical, evidenced-based recommendations for the diagnosis and treatment of PE for family practice clinicians as well as sexual medicine experts.MethodReview of the literature.ResultsThis article contains the report of the ISSM PE Guidelines Committee. It affirms the ISSM definition of PE and suggests that the prevalence is considerably lower than previously thought. Evidence-based data regarding biological and psychological etiology of PE are presented, as is population-based statistics on normal ejaculatory latency. Brief assessment procedures are delineated and validated diagnostic and treatment questionnaires are reviewed. Finally, the best practices treatment recommendations are presented to guide clinicians, both familiar and unfamiliar with PE, in facilitating treatment of their patients.ConclusionDevelopment of guidelines is an evolutionary process that continually reviews data and incorporates the best new research. We expect that ongoing research will lead to a more complete understanding of the pathophysiology as well as new efficacious and safe treatments for this sexual dysfunction. Therefore, it is strongly recommended that these guidelines be re-evaluated and updated by the ISSM every 4 years.
Teaching Neuro Images : Malignant cerebral venous thrombosis and pulmonary emboli
Dhillon, Amandeep K. , Rabinstein, Alejandro A. , Wijdicks, Eelco F. M.

Neurology | September 13, 2010 | Volume: 75 | Issue: 11 | Pages: No page available

10.1212/wnl.0b013e3181f25ef4 | PMID 20837958 Get It

Accuracy in the Use of Traditional Cun Measurement Techniques for Localizing Classical Acupoints in the Upper Extremity: An Experimental Study
Dorsher, Peter T. , Johnson, AL

Medical Acupuncture | September 13, 2010 | Volume: 22 | Issue: 3 | Pages: 191-195

10.1089/acu.2010.0759 Get It

Abstract Background: The locations of most of the 361 classical acupuncture points are determined in clinical practice by measuring their traditionally described positions using the cun system. Some data suggest the routinely taught methods of cun measurement may lead to inaccurate acupoint localizations. Objectives: To determine the accuracy of the traditional cun measuring techniques in localizing acupoints LU 4 and TE 8 compared with tape measure determination of their optimal locations, and to assess if the ability to accurately localize these points correlates with the length of acupuncture experience. Design, Setting, and Participants: Nonrandomized, experimental study conducted with 20 physician-acupuncturists on 2 adult volunteers at a medical acupuncture conference in Fall 2009. Eleven acupuncturists independently marked the location of LU 4, and 9 acupuncturists marked the location of TE 8 by traditional cun measuring techniques on the 2 volunteers, utilizing a novel point-marking method that blinded each acupuncturist from the others' point location findings. The optimal locations for the 2 acupoints were determined by direct measurement using a tape measure. Main Outcome Measures: Distances in millimeters of the clinicians' acupuncture point localizations from the optimal point positions. Results: For LU 4, the mean inaccuracy in locating this point using traditional measurement methods was 22.3 mm (range, 5-44 mm; SD = 10.9 mm). For TE 8, the mean inaccuracy was 8.4 mm (range, 1-21 mm; SD = 5.4 mm). Years of acupuncture experience (≤10 vs >10) did not affect the accuracy of clinicians' point localizations. Conclusions: Traditional cun methods routinely used to locate acupuncture points can produce enough inaccuracy in point localization that incorrect nearby acupoints could be needled inadvertently, irrespective of the amount of clinical experience of the acupuncturist. False-negative acupuncture intervention results (i.e., no beneficial clinical effect) in clinical trials could result.
Neuromuscular Paraneoplastic Syndromes: The Lambert-Eaton Myasthenic Syndrome
Prommer, Eric

Journal of Palliative Medicine | September 13, 2010 | Volume: 13 | Issue: 9 | Pages: 1159-1162

10.1089/jpm.2009.0418 | PMID 20836646 Get It

Fibrin D-Dimer Concentration, Deep Vein Thrombosis Symptom Duration, and Venous Thrombus Volume
Kurklinsky, Andrew K., Kalsi, Henna, Wysokiński, Waldemar E. , Mauck, Karen F. , Bhagra, Anjali , Havyer, Rachel D. , Thompson, Carrie A. , Hayes, Sharonne N. , McBane, Robert D. , Wysokinski, Waldemar , McBane, Robert , Hayes, Sharonne N

Angiology | September 11, 2010 | Volume: 62 | Issue: 3 | Pages: 253-256

10.1177/0003319710382416 | PMID 20834027 Get It

Introduction: To determine the relationship between fibrin D-dimer levels, symptom duration, and thrombus volume, consecutive patients with incident deep venous thrombosis (DVT) were evaluated. Methods: In a cross-sectional study design, patient symptom onset was determined by careful patient questioning. Venous thrombosis was confirmed by compression duplex ultrasonography. Thrombus volume was estimated based on patient’s femur length using a forensic anthropology method. Fibrin D-dimer was measured by latex immunoassay. Results: 72 consecutive patients with confirmed leg DVT agreed to participate. The median symptom duration at the time of diagnosis was 10 days. The median D-dimer concentration was 1050 ng/dL. The median thrombus volume was 12.92 cm 3 . D-Dimer levels correlated with estimated thrombus volume (P < .0006 CI 0.12-0.41; R 2 adjusted = .15) but not symptom duration, patient’s age, or gender. Conclusions: Despite varying symptom duration prior to diagnosis, fibrin D-dimer remains a sensitive measure of venous thrombosis and correlates with thrombus volume.