Literature DB >> 21890147

Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.

Deepika S Darbari1, Onyinye Onyekwere, Mehdi Nouraie, Caterina P Minniti, Lori Luchtman-Jones, Sohail Rana, Craig Sable, Gregory Ensing, Niti Dham, Andrew Campbell, Manuel Arteta, Mark T Gladwin, Oswaldo Castro, James G Taylor, Gregory J Kato, Victor Gordeuk.   

Abstract

OBJECTIVE: To identify factors associated with frequent severe vaso-occlusive pain crises in a contemporary pediatric cohort of patients with sickle cell anemia (SCA) enrolled in a prospective study of pulmonary hypertension and the hypoxic response in sickle cell disease. STUDY
DESIGN: Clinical and laboratory characteristics of children with SCA who had ≥3 severe pain crises requiring health care in the preceding year were compared with those of subjects with <3 such episodes.
RESULTS: Seventy-five children (20%) reported ≥3 severe pain episodes in the preceding year, and 232 (61%) had none. Frequent pain episodes were associated with older age (OR, 1.2; 95% CI, 1.1-1.3; P < .0001), α-thalassemia trait (OR 3.5; 1.6-6.7; P = .002), higher median hemoglobin (OR 1.7; 95% CI: 1.2-2.4; P < .003), and lower lactate dehydrogenase concentration (OR 1.82; 95% CI: 1.07-3.11; P = .027). Children with high pain frequency also had an increased iron burden (serum ferritin, 480 vs 198 μg/L; P = .006) and higher median tricuspid regurgitation jet velocity (2.41 vs 2.31 m/s; P = .001). Neither hydroxyurea use nor fetal hemoglobin levels were significantly different according to severe pain history.
CONCLUSIONS: In our cohort of children with SCA, increasing age was associated with higher frequency of severe pain episodes as were α-thalassemia, iron overload, higher hemoglobin and lower lactate dehydrogenase concentration, and higher tricuspid regurgitation velocity.
Copyright © 2012 Mosby, Inc. All rights reserved.

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Year:  2011        PMID: 21890147      PMCID: PMC3258348          DOI: 10.1016/j.jpeds.2011.07.018

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  30 in total

1.  Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease.

Authors:  Julie A Panepinto; David C Brousseau; Cheryl A Hillery; J Paul Scott
Journal:  Pediatr Blood Cancer       Date:  2005-02       Impact factor: 3.167

2.  Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease.

Authors:  Gregory J Kato; Vicki McGowan; Roberto F Machado; Jane A Little; James Taylor; Claudia R Morris; James S Nichols; Xunde Wang; Mirjana Poljakovic; Sidney M Morris; Mark T Gladwin
Journal:  Blood       Date:  2005-11-15       Impact factor: 22.113

3.  Design of the multicenter study of hydroxyurea in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea.

Authors:  S Charache; M L Terrin; R D Moore; G J Dover; R P McMahon; F B Barton; M Waclawiw; S V Eckert
Journal:  Control Clin Trials       Date:  1995-12

4.  GTP cyclohydrolase and tetrahydrobiopterin regulate pain sensitivity and persistence.

Authors:  Irmgard Tegeder; Michael Costigan; Robert S Griffin; Andrea Abele; Inna Belfer; Helmut Schmidt; Corina Ehnert; Jemiel Nejim; Claudiu Marian; Joachim Scholz; Tianxia Wu; Andrew Allchorne; Luda Diatchenko; Alexander M Binshtok; David Goldman; Jan Adolph; Swetha Sama; Steven J Atlas; William A Carlezon; Aram Parsegian; Jörn Lötsch; Roger B Fillingim; William Maixner; Gerd Geisslinger; Mitchell B Max; Clifford J Woolf
Journal:  Nat Med       Date:  2006-10-22       Impact factor: 53.440

5.  Asthma is associated with acute chest syndrome and pain in children with sickle cell anemia.

Authors:  Jessica H Boyd; Eric A Macklin; Robert C Strunk; Michael R DeBaun
Journal:  Blood       Date:  2006-05-11       Impact factor: 22.113

6.  Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia.

Authors:  S Charache; M L Terrin; R D Moore; G J Dover; F B Barton; S V Eckert; R P McMahon; D R Bonds
Journal:  N Engl J Med       Date:  1995-05-18       Impact factor: 91.245

Review 7.  Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease.

Authors:  F M Gill; L A Sleeper; S J Weiner; A K Brown; R Bellevue; R Grover; C H Pegelow; E Vichinsky
Journal:  Blood       Date:  1995-07-15       Impact factor: 22.113

8.  Daily assessment of pain in adults with sickle cell disease.

Authors:  Wally R Smith; Lynne T Penberthy; Viktor E Bovbjerg; Donna K McClish; John D Roberts; Bassam Dahman; Imoigele P Aisiku; James L Levenson; Susan D Roseff
Journal:  Ann Intern Med       Date:  2008-01-15       Impact factor: 25.391

9.  Prediction of adverse outcomes in children with sickle cell anemia: a study of the Dallas Newborn Cohort.

Authors:  Charles T Quinn; Nancy J Lee; Elizabeth P Shull; Naveed Ahmad; Zora R Rogers; George R Buchanan
Journal:  Blood       Date:  2007-10-01       Impact factor: 22.113

10.  Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain.

Authors:  James G Taylor; Vikki G Nolan; Laurel Mendelsohn; Gregory J Kato; Mark T Gladwin; Martin H Steinberg
Journal:  PLoS One       Date:  2008-05-07       Impact factor: 3.240

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  31 in total

Review 1.  Genetic modifiers of sickle cell disease.

Authors:  Martin H Steinberg; Paola Sebastiani
Journal:  Am J Hematol       Date:  2012-05-28       Impact factor: 10.047

2.  Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort.

Authors:  Betânia Lucena Domingues Hatzlhofer; Diego Antonio Pereira-Martins; Igor de Farias Domingos; Gabriela da Silva Arcanjo; Isabel Weinhäuser; Diego Arruda Falcão; Isabela Cristina Cordeiro Farias; Jéssica Vitória Gadelha de Freitas Batista; Luana Priscilla Laranjeira Prado; Jéssica Maria Florencio Oliveira; Thais Helena Chaves Batista; Marcondes José de Vasconcelos Costa Sobreira; Rodrigo Marcionilo de Santana; Amanda Bezerra de Sá Araújo; Manuela Albuquerque de Melo; Bruna Vasconcelos de Ancântara; Juan Luiz Coelho-Silva; Ana Beatriz Lucas de Moura Rafael; Danízia Menezes de Lima Silva; Flávia Peixoto Albuquerque; Magnun Nueldo Nunes Santos; Ana Cláudia Dos Anjos; Fernando Ferreira Costa; Aderson da Silva Araújo; Antonio Roberto Lucena-Araújo; Marcos André Cavalcanti Bezerra
Journal:  Ann Hematol       Date:  2021-02-13       Impact factor: 3.673

3.  Clinical and genetic factors are associated with pain and hospitalisation rates in sickle cell anaemia in Cameroon.

Authors:  Ambroise Wonkam; Khuthala Mnika; Valentina J Ngo Bitoungui; Bernard Chetcha Chemegni; Emile R Chimusa; Collet Dandara; Andre P Kengne
Journal:  Br J Haematol       Date:  2017-12-03       Impact factor: 6.998

4.  Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia.

Authors:  Deepika S Darbari; Mehdi Nouraie; James G Taylor; Carlo Brugnara; Oswaldo Castro; Samir K Ballas
Journal:  Eur J Haematol       Date:  2014-01-30       Impact factor: 2.997

Review 5.  Intravascular hemolysis and the pathophysiology of sickle cell disease.

Authors:  Gregory J Kato; Martin H Steinberg; Mark T Gladwin
Journal:  J Clin Invest       Date:  2017-03-01       Impact factor: 14.808

6.  Immunological role of CD4+CD28null T lymphocytes, natural killer cells, and interferon-gamma in pediatric patients with sickle cell disease: relation to disease severity and response to therapy.

Authors:  Mohsen Saleh ElAlfy; Amira Abdel Moneam Adly; Fatma Soliman ElSayed Ebeid; Deena Samir Eissa; Eman Abdel Rahman Ismail; Yasser Hassan Mohammed; Manar Elsayed Ahmed; Aya Sayed Saad
Journal:  Immunol Res       Date:  2018-08       Impact factor: 2.829

7.  Impact of early analgesia on hospitalization outcomes for sickle cell pain crisis.

Authors:  Jason Payne; Inmaculada Aban; Lee M Hilliard; Jennifer Madison; Christina Bemrich-Stolz; Thomas H Howard; Amanda Brandow; Emily Waite; Jeffrey D Lebensburger
Journal:  Pediatr Blood Cancer       Date:  2018-08-27       Impact factor: 3.167

8.  Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.

Authors:  Irene Lubega; Christopher M Ndugwa; Edison A Mworozi; James K Tumwine
Journal:  Afr Health Sci       Date:  2015-06       Impact factor: 0.927

9.  Red Blood Cell Adhesion to Heme-Activated Endothelial Cells Reflects Clinical Phenotype in Sickle Cell Disease.

Authors:  Erdem Kucukal; Anton Ilich; Nigel S Key; Jane A Little; Umut A Gurkan
Journal:  Am J Hematol       Date:  2018-06-15       Impact factor: 10.047

10.  Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia.

Authors:  Pallav Bhatnagar; Jeffrey R Keefer; James F Casella; Emily A Barron-Casella; Christopher J Bean; Craig W Hooper; Amanda B Payne; Dan E Arking; Michael R Debaun
Journal:  Pediatr Blood Cancer       Date:  2013-05-15       Impact factor: 3.167

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