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2435 citation(s) found for "Ly, Amy".

Induced Resistance to Ofatumumab-Mediated Cell Clearance Mechanisms, Including Complement-Dependent Cytotoxicity, in Chronic Lymphocytic Leukemia
Baig, Nisar A. , Lindorfer, Margaret A. , Church, Amy K., LaPlant, Betsy, Pettinger, Adam, Nowakowski, Grzegorz S. , Taylor, Ronald P. , Shanafelt, Tait D. , Zent, Clive S.

The Journal of Immunology | January 16, 2014 | Volume: 192 | Issue: 4 | Pages: 1620-1629

10.4049/jimmunol.1302954 | PMID 24431228 Get It

Abstract Ofatumumab (OFA), a human CD20-targeting mAb, kills B lymphocytes using the innate immune system including complement-dependent cytotoxicity (CDC). The efficacy of OFA in patients with chronic lymphocytic leukemia (CLL) is limited by drug resistance, which is not well characterized. To better understand mechanisms of resistance, we prospectively studied CLL cells isolated from blood samples collected before and after in vivo exposure to the initial dose of OFA therapy in 25 patients undergoing their first treatment for progressive CLL. As previously reported, OFA therapy rapidly decreased the absolute lymphocyte count, CD20 expression by CLL cells, and serum complement levels. We now show that after administration of the first dose of OFA, there was a modest rebound in the absolute lymphocyte count and serum complement levels, but substantial ongoing loss of CD20 expression by CLL cells. These post-OFA treatment CLL cells were highly resistant to OFA-mediated CDC but retained sensitivity to alemtuzumab-mediated CDC in vitro. Posttherapy serum OFA levels correlated inversely with both the amount of pretreatment circulating cell-bound CD20 and with the decrease in this value following treatment. In vitro OFA-mediated CDC did not predict clinical responses, and the patients with first-dose reactions to OFA did not have markers of increased complement activation in vivo. We propose that optimal efficacy of CD20- targeted therapy for CLL requires determining an mAb dose size and frequency that optimizes CLL killing without exceeding the capacity of the cytotoxic mechanisms and thus minimizes loss of CD20 expression in the surviving CLL cells.
Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis
Saenger, Amy K., Train, Laura, Kotzer, Katrina E. , Lagerstedt, Susan A., Hornseth, Jean M, Basu, Ananda, Baudhuin, Linnea M. , Donato, Leslie J. , Winters, Jeffrey L.

Journal of Clinical Apheresis | January 13, 2014 | Volume: 29 | Issue: 5 | Pages: 256-265

10.1002/jca.21317 | PMID 24420163 Get It

High sensitivity cardiac troponin T in patients with immunoglobulin light chain amyloidosis
Dispenzieri, Angela , Kumar, Shaji , Lacy, Martha Q. , Kyle, Robert A. , Saenger, Amy K., Grogan, Martha , Zeldenrust, Steven R., Hayman, S. R., Greipp, Philip R., Russell, Stephen J. , Dingli, David , Lust, John A., Rajkumar, S. Vincent , Jaffe, Allan S. , Gertz, Morie A. , Buadi, Francis K. , Leung, Nelson , Jaffe, Allan S. , Rajkumar, S Vincent , Dispenzieri, Angela , Russell, Stephen J , Dingli, David

Heart | January 9, 2014 | Volume: 100 | Issue: 5 | Pages: 383-388

10.1136/heartjnl-2013-304957 | PMID 24402772 Get It

Objectives To define whether the high sensitivity cardiac troponin T (hs-cTnT) assay in patients with immunoglobulin light chain amyloidosis (AL) improves risk prediction. Background Cardiac involvement is the major cause of death in patients with AL amyloidosis. Risk stratification is facilitated by cardiac biomarkers such as cardiac troponin T (cTnT) and N-terminal pro B-type natriuretic peptide (NT-proBNP). Methods Stored serum from patients with newly diagnosed AL was used to measure hs-cTnT, cTnT, and NT-proBNP. Survival modelling was performed. Results The direct numeric result from hs-cTnT measurement cannot merely be substituted for a cTnT measurement in the Mayo AL staging system. The performance of the receiver operator curve derived an hs-cTnT cut-point of 54 ng/L which improves on the value of 35 ng/L validated with the prior iteration of the assay. An alternate staging option using hs-cTnT alone—using the two thresholds 14 ng/L and 54 ng/L—performs as well as either the original Mayo AL staging system or other systems incorporating hs-cTnT. On multivariate analysis, an hs-cTnT alone staging system was independent of period of diagnosis, type of therapy, and NT-proBNP value, the last of which dropped out of the model. Alternate models were explored, but none performed better than the original system or the new hs-cTnT system. Thus, hs-cTnT can be used alone for the staging of disease prognosis. Conclusions A survival model based on hs-cTnT improves the prognostic staging of patients with AL amyloidosis, relegating NT-proBNP to a measure of cardiac response.
Certain Activating Mutations within Helix 6 of the Human Luteinizing Hormone Receptor May Be Explained by Alterations That Allow Transmembrane Regions to Activate Gs
Abell, Amy N. , Segaloff, Deborah L. , McCormick, Daniel

Molecular Endocrinology | January 8, 2014 | Volume: 12 | Issue: 12 | Pages: 1857-1869

10.1210/mend.12.12.0202 | PMID 9849960 Get It

Distal Radius Fractures and the Volar Lunate Facet Fragment: Kirschner Wire Fixation in Addition to Volar-Locked Plating
Dennison, David G., Moore, Amy M.

HAND | December 23, 2013 | Volume: 9 | Issue: 2 | Pages: 230-236

10.1007/s11552-013-9585-7 | PMID 24839427 Get It

Background The volar lunate facet fragment of a distal radius fracture may not be stabilized with volar-locked plating alone due to the small size and distal location of the fragment. Identification and stabilization of this small fragment is critical as unstable fixation may result in radiocarpal and radioulnar joint subluxation. The addition of spring wire fixation with volar plating can provide stable internal fixation of this critical fracture fragment. Methods A retrospective review (2006–2011) identified nine patients with distal radius fractures with an associated volar lunate facet fragment that were treated with volar-locked plating and spring wire fixation of the volar lunate facet fragment. Radiographic indices, range of motion, grip strength, and postoperative Patient-related wrist evaluation (PRWE) scores were obtained to assess pain and function. Results All distal radius fractures healed, and the volar lunate facet fragment reduction was maintained. The mean follow-up was 54 weeks. Mean active range of motion was 46° wrist flexion, 51° wrist extension, 80° pronation, and 68° supination. The mean grip strength was 21 Kg, achieving 66 % of the uninjured limb. The average PRWE score was 17. No patient required removal of hardware or had evidence of tendon irritation. Conclusions The addition of spring wire fixation to volar-locked plating provided stable fixation of the volar lunate facet fragment of distal radius fractures without complication. This technique addresses a limitation of volar-locked plating to control the small volar lunate facet fragment in distal radius fractures otherwise amenable to volar plating. Level of Evidence A retrospective case series, Level IV.
Short Communication: CD4 T Cell Declines Occurring During Suppressive Antiretroviral Therapy Reflect Continued Production of Casp8p41
Neuhaus, Jacqueline, Sainski, Amy M., Strausbauch, Michael, Wettstein, Peter J., Lewin, Sharon R. , Plana, Montserrat, Rizza, Stacey A. , Temesgen, Zelalem , Touloumi, Giota , Freiberg, Matthew S. , Neaton, James D. , Badley, Andrew D. , Group, for the INSIGHT SMART Study, Cummins, Nathan W. , Plana, Montserrat , Group, for the INSIGHT SMART Study, Badley, Andrew D , Nordwall, Jacqueline

AIDS Research and Human Retroviruses | December 18, 2013 | Volume: 30 | Issue: 5 | Pages: 476-479

10.1089/aid.2013.0243 | PMID 24344953 Get It

Dietary Docosahexaenoic Acid Supplementation in Children With Autism
Voigt, Robert G. , Mellon, Michael W., Katusic, Slavica K., Weaver, Amy L. , Matern, Dietrich , Mellon, Bryan, Jensen, Craig L., Barbaresi, William J.

Journal of Pediatric Gastroenterology and Nutrition | December 17, 2013 | Volume: 58 | Issue: 6 | Pages: 715-722

10.1097/mpg.0000000000000260 | PMID 24345834 Get It

ABSTRACTObjective:The aim of the study was to determine whether docosahexaenoic acid (DHA) supplementation improves the behavior of children with autism.Methods:A group of 3‐ to 10‐year‐old children with autism were randomized in a double‐blind fashion to receive a supplement containing 200 mg of DHA or a placebo for 6 months. The parents and the investigator completed the Clinical Global Impressions‐Improvement scale to rate changes in core symptoms of autism after 3 and 6 months. The parents completed the Child Development Inventory and the Aberrant Behavior Checklist, and both parents and teachers completed the Behavior Assessment Scale for Children (BASC) at enrollment and after 6 months.Results:A total of 48 children (40 [83%] boys, mean age [standard deviation] 6.1 [2.0] years) were enrolled; 24 received DHA and 24 placebo. Despite a median 431% increase in total plasma DHA levels after 6 months, the DHA group was not rated as improved in core symptoms of autism compared to the placebo group on the CGI‐I. Based on the analysis of covariance models adjusted for the baseline rating scores, parents (but not teachers) provided a higher average rating of social skills on the BASC for the children in the placebo group compared to the DHA group (P = 0.04), and teachers (but not parents) provided a higher average rating of functional communication on the BASC for the children in the DHA group compared to the placebo group (P = 0.02).Conclusions:Dietary DHA supplementation of 200 mg/day for 6 months does not improve the core symptoms of autism. Our results may have been limited by inadequate sample size.
Associations between Cigarette Smoking, Hormone Therapy, and Folate Intake with Incident Colorectal Cancer by TP53 Protein Expression Level in a Population-Based Cohort of Older Women
Tillmans, Lori S. , Vierkant, Robert A. , Wang, Alice H., Samadder, N. Jewel , Lynch, Charles F. , Anderson, Kristin E. , French, Amy J. , Haile, Robert W. , Harnack, Lisa , Potter, John D. , Smyrk, Thomas C. , Thibodeau, Stephen N. , Cerhan, James R. , Slager, Susan L. , Limburg, Paul J. , Cerhan, James R , Vierkant, Robert A , Haile, Robert W , Potter, John D

Cancer Epidemiology, Biomarkers & Prevention | December 17, 2013 | Volume: 23 | Issue: 2 | Pages: 350-355

10.1158/1055-9965.epi-13-0780 | PMID 24343843 Get It

Abstract Cigarette smoking (CS), hormone therapy (HT), and folate intake (FI) are each thought to influence colorectal cancer risk, but the underlying molecular mechanisms remain incompletely defined. The TP53 (p53) protein, encoded by the TP53 tumor-suppressor gene that is commonly mutated in colorectal cancer, can be readily assessed to differentiate biologically distinct colorectal cancer subtypes. In this prospective cohort study, we examined CS-, HT-, and FI-associated colorectal cancer risks by TP53 protein expression level among Iowa Women's Health Study (IWHS) participants. The IWHS recruited 41,836 randomly selected Iowa women, ages 55 to 69 years, with a valid driver's license at study entry in 1986. Self-reported exposure variables were assessed at baseline. Incident colorectal cancer cases were ascertained by annual linkage with the Iowa Cancer Registry. Archived, paraffin-embedded tissue specimens were collected and evaluated for TP53 protein expression by immunohistochemistry. Multivariate Cox regression models were fit to estimate relative risks (RR) and 95% confidence intervals (CI) for associations between CS, HT, or FI and TP53-defined colorectal cancer subtypes. Informative environmental exposure and protein expression data were available for 492 incident colorectal cancer cases: 222 (45.1%) TP53 negative, 72 (14.6%) TP53 low, and 198 (40.2%) TP53 high. Longer duration (>5 years) of HT was inversely associated with TP53 high colorectal cancers (RR, 0.50; 95% CI, 0.27–0.94). No other statistically significant associations were observed. These data support possible heterogeneous effects from HT on TP53-related pathways of colorectal carcinogenesis in older women. Cancer Epidemiol Biomarkers Prev; 23(2); 350–5. ©2013 AACR.
American Thyroid Association Statement on Optimal Surgical Management of Goiter
Chen, Amy Y. , Bernet, Victor , Carty, Sally E. , Ganly, Ian , Inabnet, William B. , Shaha, Ashok R. , Davies, Terry F.

Thyroid® | December 3, 2013 | Volume: 24 | Issue: 2 | Pages: 181-189

10.1089/thy.2013.0291 | PMID 24295043 Get It

Background: Goiter, or benign enlargement of the thyroid gland, can be asymptomatic or can cause compression of surrounding structures such as the esophagus and/or trachea. The options for medical treatment of euthyroid goiter are short-lived and are limited to thyroxine hormone suppression and radioactive iodine ablation. The objective of this statement article is to discuss optimal surgical management of goiter. Methods: A task force was convened by the Surgical Affairs Committee of the American Thyroid Association and was tasked with writing of this article. Results/Conclusions: Surgical management is recommended for goiters with compressive symptoms. Symptoms of dyspnea, orthopnea, and dysphagia are more commonly associated with thyromegaly, in particular, substernal goiters. Several studies have demonstrated improved breathing and swallowing outcomes after thyroidectomy. With careful preoperative testing and thoughtful consideration of the type of anesthesia, including the type of intubation, preparation for surgery can be optimized. In addition, planning the extent of surgery and postoperative care are necessary to achieve optimal results. Close collaboration of an experienced surgical and anesthesia team is essential for induction and reversal of anesthesia. In addition, this team must be cognizant of complications from massive goiter surgery such as bleeding, airway distress, recurrent laryngeal nerve injury, and transient hypoparathyroidism. With careful preparation and teamwork, successful thyroid surgery can be achieved.
Decline in ACEI/ARB Prescribing as Heart Failure Core Metrics Improve During Computer-Based Clinical Decision Support
Naessens, James M. , Klarich, Mark J., Leutink, Dorinda J., Peterson, James A. , Wagie, Amy E., Manning, Dennis M., Qian, Qi , Caraballo, Pedro J.

American Journal of Medical Quality | November 19, 2013 | Volume: 29 | Issue: 4 | Pages: 300-307

10.1177/1062860613509265 | PMID 24249835 Get It