Clinical severity in sickle cell disease: the challenges of definition and prognostication

被引:85
作者
Quinn, Charles T. [1 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Hematol, 3333 Burnet Ave, Cincinnati, OH 45220 USA
关键词
Biomarkers; disease severity; phenotype; prediction; prognosis; sickle cell disease; sickle cell anemia; prevention; survival; outcomes; models; ACUTE CHEST SYNDROME; SERUM BILIRUBIN LEVELS; 1A PROMOTER POLYMORPHISMS; PHOSPHOLIPASE A(2) LEVELS; FETAL-HEMOGLOBIN; ALPHA-THALASSEMIA; PULMONARY-HYPERTENSION; RISK-FACTORS; TRANSCRANIAL DOPPLER; ADVERSE OUTCOMES;
D O I
10.1177/1535370216640385
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Sickle cell disease (SCD) is a monogenic, yet highly phenotypically variable disease with multisystem pathology. This manuscript provides an overview of many of the known determinants, modifiers, and correlates of disease severity in SCD. Despite this wealth of data, modeling the variable and multisystem pathology of SCD continues to be difficult. The current status of prediction of specific adverse outcomes and global disease severity in SCD is also reviewed, highlighting recent successes and ongoing challenges.
引用
收藏
页码:679 / 688
页数:10
相关论文
共 63 条
  • [1] THE USE OF TRANSCRANIAL ULTRASONOGRAPHY TO PREDICT STROKE IN SICKLE-CELL DISEASE
    ADAMS, R
    MCKIE, V
    NICHOLS, F
    CARL, E
    ZHANG, DL
    MCKIE, K
    FIGUEROA, R
    LITAKER, M
    THOMPSON, W
    HESS, D
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (09) : 605 - 610
  • [2] Prevention of a first stroke by transfusions in children with sickle, cell anemia and abnormal results on transcranial Doppler ultrasonography
    Adams, RJ
    McKie, VC
    Hsu, L
    Files, B
    Vichinsky, E
    Pegelow, C
    Abboud, M
    Gallagher, D
    Kutlar, A
    Nichols, FT
    Bonds, DR
    Brambilla, D
    Woods, G
    Olivieri, N
    Driscoll, C
    Miller, S
    Wang, W
    Hurlett, A
    Scher, C
    Berman, B
    Carl, E
    Jones, AM
    Roach, ES
    Wright, E
    Zimmerman, RA
    Waclawiw, M
    Pearson, H
    Powars, D
    Younkin, D
    El-Gammal, T
    Seibert, J
    Moye, L
    Espeland, M
    Murray, R
    McKinley, R
    McKinley, S
    Hagner, S
    Weiner, S
    Estow, S
    Yelle, M
    Brock, K
    Carter, E
    Chiarucci, K
    Debarr, M
    Feron, P
    Harris, S
    Hoey, L
    Jacques, K
    Kuisel, L
    Lewis, N
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (01) : 5 - 11
  • [3] The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, βS-globin gene haplotype, co-inherited α-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia
    Adekile, A
    Kutlar, F
    McKie, K
    Addington, A
    Elam, D
    Holley, L
    Clair, B
    Kutlar, A
    [J]. EUROPEAN JOURNAL OF HAEMATOLOGY, 2005, 75 (02) : 150 - 155
  • [4] Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans
    Akinsheye, Idowu
    Solovieff, Nadia
    Duyen Ngo
    Malek, Anita
    Sebastiani, Paola
    Steinberg, Martin H.
    Chui, David H. K.
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2012, 87 (02) : 217 - 219
  • [5] Fetal hemoglobin in sickle cell anemia
    Akinsheye, Idowu
    Alsultan, Abdulrahman
    Solovieff, Nadia
    Duyen Ngo
    Baldwin, Clinton T.
    Sebastiani, Paola
    Chui, David H. K.
    Steinberg, Martin H.
    [J]. BLOOD, 2011, 118 (01) : 19 - 27
  • [6] AlFadhli S, 2013, PLOS ONE, V8
  • [7] Secretory phospholipase A2 levels in patients with sickle cell disease and acute chest syndrome
    Ballas, Samir K.
    Files, Beatrice
    Luchtman-Jones, Lori
    Benjamin, Lennette
    Swerdlow, Paul
    Hilliard, Lee
    Coates, Thomas
    Abboud, Miguel
    Wojtowicz-Praga, Slawomir
    Kuypers, Frans A.
    Grindel, J. Michael
    [J]. HEMOGLOBIN, 2006, 30 (02) : 165 - 170
  • [8] Glucose-6-Phosphate Dehydrogenase Deficiency in Brazilian Children With Sickle Cell Anemia is not Associated With Clinical Ischemic Stroke or High-Risk Transcranial Doppler
    Belisario, Andre Rolim
    Sales, Rahyssa Rodrigues
    Toledo, Nayara Evelin
    Velloso-Rodrigues, Cibele
    Silva, Celia Maria
    Viana, Marcos Borato
    [J]. PEDIATRIC BLOOD & CANCER, 2016, 63 (06) : 1046 - 1049
  • [9] Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study
    Benkerrou, Malika
    Alberti, Corinne
    Couque, Nathalie
    Haouari, Zinedine
    Ba, Aissatou
    Missud, Florence
    Boizeau, Priscilla
    Holvoet, Laurent
    Ithier, Ghislaine
    Elion, Jacques
    Baruchel, Andre
    Ducrocq, Rolande
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2013, 163 (05) : 646 - 654
  • [10] G6PD deficiency, absence of α-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia
    Bernaudin, Francoise
    Verlhac, Suzanne
    Chevret, Sylvie
    Torres, Martine
    Coic, Lena
    Arnaud, Cecile
    Kamdem, Annie
    Hau, Isabelle
    Neonato, Maria Grazia
    Delacourt, Christophe
    [J]. BLOOD, 2008, 112 (10) : 4314 - 4317