Literature DB >> 25236783

Factors associated with growth and blood pressure patterns in children with sickle cell anemia: Silent Cerebral Infarct Multi-Center Clinical Trial cohort.

Rachel B Wolf1, Benjamin R Saville, Dionna O Roberts, Rachel B Fissell, Adetola A Kassim, Gladstone Airewele, Michael R DeBaun.   

Abstract

Individuals with sickle cell anemia (SCA) exhibit delayed growth trajectories and lower blood pressure (BP) measurements than individuals without SCA. We evaluated factors associated with height, weight, and BP and established reference growth curves and BP tables using data from the Silent Cerebral Infarct Multi-Center Clinical (SIT) Trial (NCT00072761). Quantile regression models were used to determine the percentiles of growth and BP measurements. Multivariable quantile regression was used to test associations of baseline variables with height, weight, and BP measurements. Height and weight measurements were collected from a total of 949 participants with median age of 10.5 years [Interquartile range (IQR) 8.2-12.9] and median follow-up time of 3.2 years (IQR 1.8-4.7, range 0-12.9). Serial BP measurements were collected from a total of 944 and 943 participants, respectively, with median age of 10.6 years (IQR = 8.3-12.9 years), and median follow-up time of 3.3 years (IQR = 1.7-4.8). Multivariable quantile regression analysis revealed that higher hemoglobin measurements at baseline were associated with greater height (P < 0.001), weight (P = 0.000), systolic BP (P < 0.001), and diastolic BP (P = 0.003) measurements. We now provide new reference values for height, weight, and BP measurements that are now readily available for medical management.
© 2014 Wiley Periodicals, Inc.

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Year:  2014        PMID: 25236783     DOI: 10.1002/ajh.23854

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  14 in total

Review 1.  Interventions for preventing silent cerebral infarcts in people with sickle cell disease.

Authors:  Lise J Estcourt; Patricia M Fortin; Sally Hopewell; Marialena Trivella; Carolyn Doree; Miguel R Abboud
Journal:  Cochrane Database Syst Rev       Date:  2017-05-13

2.  Severe anemia early in life as a risk factor for sickle-cell kidney disease.

Authors:  Inmaculada Aban; Sujatha Baddam; Lee M Hilliard; Thomas H Howard; Daniel I Feig; Jeffrey D Lebensburger
Journal:  Blood       Date:  2016-12-05       Impact factor: 22.113

3.  End points for sickle cell disease clinical trials: renal and cardiopulmonary, cure, and low-resource settings.

Authors:  Ann T Farrell; Julie Panepinto; Ankit A Desai; Adetola A Kassim; Jeffrey Lebensburger; Mark C Walters; Daniel E Bauer; Rae M Blaylark; Donna M DiMichele; Mark T Gladwin; Nancy S Green; Kathryn Hassell; Gregory J Kato; Elizabeth S Klings; Donald B Kohn; Lakshmanan Krishnamurti; Jane Little; Julie Makani; Punam Malik; Patrick T McGann; Caterina Minniti; Claudia R Morris; Isaac Odame; Patricia Ann Oneal; Rosanna Setse; Poornima Sharma; Shalini Shenoy
Journal:  Blood Adv       Date:  2019-12-10

4.  Effect of Sickle Cell Anemia Therapies on the Natural History of Growth and Puberty Patterns.

Authors:  Vishnu Nagalapuram; Varsha Kulkarni; Justin Leach; Inmaculada Aban; Krishnaveni Sirigaddi; Jeffrey D Lebensburger; Pallavi Iyer
Journal:  J Pediatr Hematol Oncol       Date:  2019-11       Impact factor: 1.289

5.  Low educational level of head of household, as a proxy for poverty, is associated with severe anaemia among children with sickle cell disease living in a low-resource setting: evidence from the SPRING trial.

Authors:  Halima Bello-Manga; Aisha A Galadanci; Shehu Abdullahi; Shehi Ali; Binta Jibir; Safiya Gambo; Lawal Haliru; Lori C Jordan; Muktar H Aliyu; Mark Rodeghier; Adetola A Kassim; Michael R DeBaun; Najibah A Galadanci
Journal:  Br J Haematol       Date:  2020-05-16       Impact factor: 6.998

6.  Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease.

Authors:  Lise J Estcourt; Ruchika Kohli; Sally Hopewell; Marialena Trivella; Winfred C Wang
Journal:  Cochrane Database Syst Rev       Date:  2020-07-27

7.  Interventions for preventing silent cerebral infarcts in people with sickle cell disease.

Authors:  Lise J Estcourt; Catherine Kimber; Sally Hopewell; Marialena Trivella; Carolyn Doree; Miguel R Abboud
Journal:  Cochrane Database Syst Rev       Date:  2020-04-06

8.  Unmasking hypertension in children and adolescents with sickle/beta-thalassemia.

Authors:  Stella Stabouli; Christina Antza; Eleni Papadopoulou; Aikaterini Teli; Vasilios Kotsis; Marina Economou
Journal:  J Clin Hypertens (Greenwich)       Date:  2020-08-06       Impact factor: 3.738

Review 9.  Hypertension and childhood stroke.

Authors:  Juan C Kupferman; Marc B Lande; Stella Stabouli; Dimitrios I Zafeiriou; Steven G Pavlakis
Journal:  Pediatr Nephrol       Date:  2020-04-29       Impact factor: 3.714

10.  Blood transfusions for treating acute chest syndrome in people with sickle cell disease.

Authors:  Roya Dolatkhah; Saeed Dastgiri
Journal:  Cochrane Database Syst Rev       Date:  2020-01-16
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