keyword
https://read.qxmd.com/read/38644415/mendelian-randomization-of-circulating-proteome-identifies-ifn-%C3%AE-as-a-druggable-target-in-aplastic-anemia
#1
JOURNAL ARTICLE
Shanshan Qin, Yingxin Jiang, Yang Ou, Yanxia Zhan, Lili Ji, Pengcheng Xu, Xia Shao, Hao Chen, Tong Chen, Yunfeng Cheng
BACKGROUND: Aplastic anemia (AA) is a kind of bone marrow failure (BMF) characterized by pancytopenia with hypoplasia/aplasia of bone marrow. Immunosuppressive therapy and bone marrow transplantation are effective methods to treat severe aplastic anemia. However, the efficacy is limited by complications and the availability of suitable donors. This study aimed to determine whether any circulating druggable protein levels may have causal effects on AA and provide potential novel drug targets for AA...
April 22, 2024: Annals of Hematology
https://read.qxmd.com/read/38640200/multicenter-phase-1-study-of-etavopivat-ft-4202-treatment-for-up-to-12-weeks-in-patients-with-sickle-cell-disease
#2
JOURNAL ARTICLE
Santosh L Saraf, Robert Ward Hagar, Modupe Idowu, Ifeyinwa Osunkwo, Kimberly Cruz, Frans A Kuypers, R Clark Brown, James Geib, Maria D Ribadeneira, Patricia Schroeder, Eric Wu, Sanjeev Forsyth, Patrick F Kelly, Theodosia A Kalfa, Marilyn J Telen
Etavopivat is an investigational, once-daily, oral, selective erythrocyte pyruvate kinase (PKR) activator. A multicenter, randomized, placebo-controlled, double-blind, 3-part, phase 1 study (https://clinicaltrials.gov/study/NCT03815695) was conducted to characterize the safety and clinical activity of etavopivat. Thirty-six patients with sickle cell disease (SCD) were enrolled into 4 cohorts: one single-dose; two multiple ascending doses; one open-label [OL]. In the OL cohort, 15 patients (median age 33.0 [range, 17‒55] years received 400-mg etavopivat once daily for 12 weeks; 14 completed treatment...
April 19, 2024: Blood Advances
https://read.qxmd.com/read/38627593/end-tidal-carbon-monoxide-concentrations-measured-within-48%C3%A2-hours-of-birth-predict-hemolytic-hyperbilirubinemia
#3
JOURNAL ARTICLE
Xiaoqin Cheng, Bingchun Lin, Yong Yang, Yanliang Yu, Yongping Fu, Chuanzhong Yang
OBJECTIVES: To determine, among neonates at-risk for hyperbilirubinemia, whether measuring end-tidal carbon monoxide concentration (ETCOc) twice before 48 hours could identify those who would develop hyperbilirubinemia and differentiate hemolytic vs. non-hemolytic causes. METHODS: Prospective study on neonates meeting criteria "at-risk for hyperbilirubinemia." Routine bilirubin measurements and 10-day follow-up were used to categorize neonates as; (1) normal (no hyperbilirubinemia, all bilirubins <95th percentile of Bhutani nomogram), (2) having hemolytic hyperbilirubinemia (bilirubin ≥95th percentile, DAT+, elevated retic, or G6PD+), or (3) having non-hemolytic hyperbilirubinemia...
April 16, 2024: Journal of Perinatology: Official Journal of the California Perinatal Association
https://read.qxmd.com/read/38615657/efficacy-safety-and-quality-of-life-of-pegcetacoplan-in-japanese-patients-with-paroxysmal-nocturnal-hemoglobinuria-treated-within-the-phase-3-pegasus-trial
#4
JOURNAL ARTICLE
Hisakazu Nishimori, Hideyuki Nakazawa, Shinobu Tamura, Toshiki Uchida, Kensuke Usuki, Johan Szamosi, Régis Peffault de Latour, Alexander Röth, Jens Panse
INTRODUCTION: Pegcetacoplan, the first approved proximal complement C3 inhibitor, showed superiority to eculizumab in improving hemoglobin levels and clinical outcomes in the phase 3 PEGASUS study in patients with paroxysmal nocturnal hemoglobinuria (PNH) and inadequate response to eculizumab. METHODS: This analysis evaluates the efficacy and safety of pegcetacoplan for Japanese patients in PEGASUS, as they are known for different clinicopathologic features compared to non-Asian patients...
April 12, 2024: Acta Haematologica
https://read.qxmd.com/read/38605807/collage-of-cases-and-brief-review-of-the-laboratory-diagnosis-and-molecular-testing-in-autoimmune-haemolytic-anaemia
#5
REVIEW
Harkiran Arora, Shalini Trivedi, Pooja Jain, Udita Singhal, Arunpreet Kaur, Aditi Raina
Autoimmune haemolytic anaemia (AIHA) is an acquired heterogenous clinical entity with variable presentations like acute haemolysis or mild, chronic haemolysis compounded with acute exacerbation in winters or fatal uncompensated haemolysis. A step-wise approach to the diagnosis and characterisation of AIHA should be undertaken, firstly the diagnosis of haemolysis followed by the establishment of immune nature with the aid of direct agglutination tests (DAT). Simultaneously the other causes of immune haemolysis need to be excluded too...
February 2024: Journal of Family Medicine and Primary Care
https://read.qxmd.com/read/38595948/comparison-of-blood-profiles-between-housed-and-grazing-korean-indigenous-cattle-hanwoo
#6
JOURNAL ARTICLE
Youngjun Kim, Ji-Yeong Ku, Kwang-Man Park, Jonghun Baek, Kyoung-Seong Choi, Jinho Park
The objective of this study was to compare the hematology profiles of Korean indigenous cattle (Hanwoo) raised in a barn (housed) or on pasture (grazing). Our findings showed significant differences in the red blood cell (RBC) profiles of these 2 groups. When compared to cattle raised in a barn, a significant decrease in hematocrit ( P = 0.000), hemoglobin ( P = 0.000), and red blood cells (RBCs) ( P = 0.000) and a significant increase in mean cell volume ( P = 0.015) and reticulocytes ( P = 0.000) were observed in grazing cattle, which indicate regenerative anemia...
April 2024: Canadian Journal of Veterinary Research
https://read.qxmd.com/read/38583826/tcr%C3%AE-%C3%AE-depleted-hematopoietic-stem-cell-transplant-and-third-party-cd45ra-depleted-adoptive-cell-therapy-for-treatment-of-post-transplant-parvovirus-b19-aplastic-crisis
#7
Manpin Zhang, Chengjuan Luo, Jianmin Wang, Hua Zhu, Changying Luo, Xia Qin, Xiaohang Huang, Yuchen Lin, Jing Chen
This is a case report of a 6-year-old girl with relapsed B cell acute lymphoblastic leukemia in which adoptive cell therapy was applied successfully to treat refractory human parvovirus (HPV) B19 infection. Allogenic chimeric antigen receptor (CAR) T-cell therapy (bispecific CD19/CD22) was bridged to hematopoietic stem cell transplantation (HSCT) using a haploidentical paternal donor. However, HPV B19 DNAemia progressed and transfusion-related graft versus host disease occurred. After finding a third-party related donor with a better HLA match, haploidentical HPV B19-seropositive CD45RA+ depleted cells (16...
April 5, 2024: International Journal of Infectious Diseases: IJID
https://read.qxmd.com/read/38582651/utility-of-hemoglobin-electrophoresis-to-distinguish-between-severe-delayed-hemolytic-transfusion-reaction-versus-hyperhemolysis-syndrome
#8
JOURNAL ARTICLE
Robert Lukin, Jennie Y Law, Parvez M Lokhandwala
Delayed hemolytic transfusion reaction (DHTR) and hyperhemolysis syndrome (HHS) are both complications of red blood cell transfusions in patients with sickle cell disease.Clinically, both present with hemolysis and can be difficult to differentiate. Hemoglobin electrophoresis may aid in the diagnosis. Herein we describe a case in which a patient with hemoglobin SC disease presented with features of severe hemolysis several days after initiation of red blood cell exchange. Increase in reticulocyte count and complete absence of hemoglobin A on electrophoresis during this event supported the diagnosis of severe DHTR, indicating a rapid and selective destruction of the transfused red blood cells...
March 27, 2024: Transfusion and Apheresis Science
https://read.qxmd.com/read/38581299/effects-of-cd34-cell-dose-on-engraftment-and-long-term-outcomes-after-allogeneic-bone-marrow-transplantation
#9
JOURNAL ARTICLE
Takashi Oyama, Shin-Ichiro Fujiwara, Ryutaro Tominaga, Daizo Yokoyama, Atsuto Noguchi, Shuka Furuki, Shunsuke Koyama, Rui Murahashi, Hirotomo Nakashima, Kazuki Hyodo, Takashi Ikeda, Shin-Ichiro Kawaguchi, Yumiko Toda, Takashi Nagayama, Kento Umino, Daisuke Minakata, Kaoru Morita, Masahiro Ashizawa, Chihiro Yamamoto, Kaoru Hatano, Kazuya Sato, Ikuko Otsuki, Ken Ohmine, Yoshinobu Kanda
BACKGROUND: The number of CD34+ cells in the graft is generally associated with time to engraftment and survival in transplantation using cord blood or allogeneic peripheral blood stem cells. However, the significance of abundant CD34+ in bone marrow transplantation (BMT) remained unclear. METHODS: We retrospectively reviewed 207 consecutive adult patients who underwent their first BMT at Jichi Medical University between January 2009 and June 2021. RESULTS: The median nucleated cell count (NCC) and CD34+ cell dose were 2...
April 2024: Clinical Transplantation
https://read.qxmd.com/read/38581079/when-you-think-you-should-transfuse%C3%A2-don-t
#10
JOURNAL ARTICLE
Richard R Gammon, Harold Alvarez, Camila Masias, Nancy Benitez, Claribel Resto
A 48-year-old female presented to the emergency department with severe fatigue. Admission laboratory test results were hemoglobin 6.6 g/dL, platelet count 287,000/μL, and white blood cell count 25,200/μL. Lactate dehydrogenase was elevated at 898 U/L, haptoglobin was markedly decreased (< 31 mg/dL), indirect bilirubin was elevated (5.3 mg/dL), and the absolute reticulocyte count was low at 0.0050/μL. A sample was sent to the immunohematology reference laboratory. The direct antiglobulin test immunoglobulin G was negative; C3 was 1+...
April 6, 2024: Laboratory Medicine
https://read.qxmd.com/read/38580494/consensus-of-the-brazilian-association-of-hematology-hemotherapy-and-cellular-therapy-on-patient-blood-management-assessment-and-management-of-postoperative-anemia
#11
JOURNAL ARTICLE
Bruno Deltreggia Benites, Mariana Munari Magnus, Lorena Costa, Denise Menezes Brunetta, Roseny Dos Reis Rodriges, Susankerle de Oliveira Costa Alves, Gil Cunha De Santis, Silvia Renata Cornélio Parolin Rizzo, Guilherme Rabello, Dante Mario Langhi Junior
Postoperative anemia is a complex clinical issue that requires attention due to its ramifications on the patient's recovery and prognosis. Originating from multiple determinants, such as intraoperative blood loss, hemolysis, nutritional deficiencies, systemic inflammation and impact on the bone marrow, postoperative anemia has varied and often challenging presentations. Patients undergoing major surgical procedures, in particular, are susceptible to developing anemia due to the considerable associated blood loss...
March 19, 2024: Hematology, Transfusion and Cell Therapy
https://read.qxmd.com/read/38567942/evaluation-of-haematological-parameters-in-haemolytic-anaemia-caused-by-tick-borne-pathogens-in-grazing-cattle
#12
JOURNAL ARTICLE
Youngjun Kim, Ji-Young Ku, Youngwoo Jung, Young-Hwan Lim, Min-Jeong Ji, Yu-Jin Park, Hyung-Chul Cho, Kyoung-Seong Choi, Jinho Park
BACKGROUND: No tick-borne pathogens (TBPs) causing haemolytic anaemia in cattle have been reported, except Theileria orientalis and complete blood count (CBC) profile is the only haematological parameter to determine the severity of regenerative haemolytic anaemia. OBJECTIVES: To identify the causative agents of TBP-induced haemolytic anaemia and determine haematological parameters that indicate haemolytic anaemia in grazing cattle. METHODS: Eighty-two Korean indigenous cattle (Hanwoo) were divided into two groups: grazing (n = 67) and indoor (n = 15) groups...
May 2024: Veterinary Medicine and Science
https://read.qxmd.com/read/38563004/effects-of-three-weeks-base-training-at-moderate-simulated-altitude-with-or-without-hypoxic-residence-on-exercise-capacity-and-physiological-adaptations-in-well-trained-male-runners
#13
JOURNAL ARTICLE
Longyan Yi, Jian Wu, Bing Yan, Yang Wang, Menghui Zou, Yimin Zhang, Feifei Li, Junqiang Qiu, Olivier Girard
OBJECTIVES: To test the hypothesis that 'live high-base train high-interval train low' (HiHiLo) altitude training, compared to 'live low-train high' (LoHi), yields greater benefits on performance and physiological adaptations. METHODS: Sixteen young male middle-distance runners (age, 17.0 ± 1.5 y; body mass, 58.8 ± 4.9 kg; body height, 176.3 ± 4.3 cm; training years, 3-5 y; training distance per week, 30-60 km.wk-1 ) with a peak oxygen uptake averaging ~65 ml...
2024: PeerJ
https://read.qxmd.com/read/38560977/uncovering-predictors-of-low-hippocampal-volume-evidence-from-a-large-scale-machine-learning-based-study-in-the-uk-biobank
#14
JOURNAL ARTICLE
Yigizie Yeshaw, Iqbal Madakkatel, Anwar Mulugeta, Amanda Lumsden, Elina Hyppönen
INTRODUCTION: Hippocampal atrophy is an established biomarker for conversion from the normal ageing process to developing cognitive impairment and dementia. This study used a novel hypothesis-free machine-learning approach, to uncover potential risk factors of lower hippocampal volume using information from the world's largest brain imaging study. METHODS: A combination of machine learning and conventional statistical methods were used to identify predictors of low hippocampal volume...
April 1, 2024: Neuroepidemiology
https://read.qxmd.com/read/38556531/gilteritinib-combined-with-venetoclax-and-azacitidine-for-relapsed-acute-myeloid-leukemia-cocurrent-with-pure-red-cell-aplasia-after-allogeneic-hematopoietic-stem-cell-transplantation-a-case-report
#15
JOURNAL ARTICLE
Jiawen Wang, Han Zhu, Kourong Miao
Pure red cell aplasia (PRCA) is a rare bone marrow (BM) disorder characterized by ineffective erythropoiesis, reduced reticulocyte count, normocytic anemia, and the absence of erythroid precursors. Here, we present a rare instance of PRCA occurring after ABO-matched allo-HSCT in a refractory/relapsed acute myeloid leukemia (R/R AML) patient. In this case, the patient received a combination treatment of Gilteritinib, Venetoclax, and Azacitidine. Remarkably, this treatment not only reduced myeloblasts but also facilitated the restoration of erythroid hematopoiesis...
April 1, 2024: Annals of Hematology
https://read.qxmd.com/read/38554748/etiologies-and-outcomes-of-normocytic-anemia-in-children
#16
JOURNAL ARTICLE
Emily Equitz, Jacquelyn M Powers, Susan Kirk
OBJECTIVE: To characterize the evaluation and outcomes of children referred to pediatric hematology for normocytic anemia. STUDY DESIGN: Retrospective cohort study of children aged 0 to 21 years referred to a tertiary pediatric hematology clinic for normocytic anemia from 2019 through 2021. Normocytic anemia was defined as a low hemoglobin and normal mean corpuscular volume, per the referring laboratory reference range. RESULTS: Two-hundred seventy-one patients (48% female, median age 5...
March 28, 2024: Journal of Pediatrics
https://read.qxmd.com/read/38528249/positive-response-of-a-hemodialysis-patient-with-pure-red-cell-aplasia-on-recombinant-human-erythropoietin-therapy-to-cyclosporine-and-roxadustat
#17
JOURNAL ARTICLE
Xuejuan Ma, Pearl Pai, Wenjuan Zhu, Xiaowei Chen, Liwen Cui
Recombinant human erythropoietin (rHuEPO) is commonly used to treat anemia associated with chronic kidney disease (CKD). EPO-induced Pure Red Cell Aplasia (PRCA) is a rare condition of profound anemia with EPO treatment. Upon finding the development of EPO-induced PRCA, the treatment requires immediate withdrawal of EPO therapy and initiate new treatments with immunosuppression or renal transplantation. Anti-EPO antibody assay is not always positive in EPO-induced PRCA. Here, we report a case on the sudden development of PRCA in a hemodialysis patient receiving EPO and how we treated the condition successfully with cyclosporine and subsequently maintained the hemoglobin with Roxadustat, a hypoxia-inducible factor prolyl hydroxylase inhibitor (HIF-PHI)...
March 25, 2024: CEN Case Reports
https://read.qxmd.com/read/38506013/-not-available
#18
JOURNAL ARTICLE
Maria Winther Gunnes, Andreas Benneche, Anne Grete Bechensteen
BACKGROUND: Anemia in children is common and finding the underlying cause is often uncomplicated. However, in some cases, the underlying diagnosis is rare and difficult to diagnose. CASE PRESENTATION: A toddler presented with severe anemia with normal red cell indices and a low reticulocyte count. The remaining hematological parameters were normal, bar a slight thrombocytosis. At this point a diagnosis of transient erythroblastopenia of childhood (TEC) was made...
March 19, 2024: Tidsskrift for Den Norske Lægeforening: Tidsskrift for Praktisk Medicin, Ny Række
https://read.qxmd.com/read/38494323/-a-kiss-that-took-my-legs-away-a-rare-presentation-of-epstein-barr-virus-in-the-older-population
#19
Hussain Mahmood, Marwah Kiani, Yasser Madani
We present the case of a 70-year-old woman presenting with nausea, diarrhoea and a generalised rash. Initial blood tests revealed obstructive deranged liver function tests and low haemoglobin. A haemolysis screen revealed raised reticulocytes, low haptoglobin and a positive direct antiglobulin test. 6 days into her admission, she developed lower limb weakness and loss of sensation. MRI spine showed no significant findings. Cerebrospinal fluid showed raised white blood cell count and raised protein. Nerve conduction studies were normal...
November 2023: Clinical Medicine: Journal of the Royal College of Physicians of London
https://read.qxmd.com/read/38462913/integration-of-network-pharmacology-and-experimental-validation-to-explore-jixueteng-yinyanghuo-herb-pair-alleviate-cisplatin-induced-myelosuppression
#20
JOURNAL ARTICLE
Yi Liu, Shuying Dai, Yixiao Xu, Yuying Xiang, Yao Zhang, Zeting Xu, Lin Sun, Gao-Chen-Xi Zhang, Qijin Shu
Jixueteng, the vine of the bush Spatholobus suberectus Dunn., is widely used to treat irregular menstruation and arthralgia. Yinyanghuo, the aboveground part of the plant Epimedium brevicornum Maxim., has the function of warming the kidney to invigorate yang. This research aimed to investigate the effects and mechanisms of the Jixueteng and Yinyanghuo herbal pair (JYHP) on cisplatin-induced myelosuppression in a mice model. Firstly, ultra-high performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) screened 15 effective compounds of JYHP decoction...
2024: Integrative Cancer Therapies
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