The effect of sickle cell anemia on the linear growth of Nigerian children.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Volume: 34

Issue: 10

Year of Publication: 2022

Affiliated Institutions:  Department of Paediatrics, University of Nigeria Ituku Ozalla Campus, Enugu, Nigeria. Department of Mental Health, Nnamdi Azikiwe University, Awka, Anambra State and Federal Neuropsychiatric Hospital, Enugu, Nigeria. Usman Danfodio University, Sokoto, Nigeria. Federal Teaching Hospital, Ebonyi State University, Abakaliki, Nigeria.

Abstract summary 

Despite the high prevalence of children with sickle cell anaemia (SCA) in West Africa, there is paucity of data on the height velocity and prevalence of growth failure in SCA patients. With advances in clinical care of SCA patients, could there be a spatial and secular trend in the growth pattern of these children? Hence, the compelling needs to embark on this study. The objectives of the study were to determine the prevalence of growth failure among patients with SCA and its correlation with age, gender and age at diagnosis.A Prospective longitudinal study of a cohort of sickle cell anaemic paediatric patients from Pediatrics SCA Clinic, University of Nigeria Teaching Hospital, Ituku Ozalla. Patients were enrolled over a period of two years using a non-parametric convenient sampling method. Their heights were measured at baseline, three months, six months and at 12 months intervals and subsequently plotted on a standard WHO growth chart. The height velocities at different monthly intervals were calculated and compared with the WHO standard normal linear growth rates) for children (used as control) to identify those with GF. (i.e. <10th percentile). The main outcome measures were the mean height velocities at different months' intervals calculated and compared using the repeated measurement analysis of variance (ANOVA) and the Wilcoxon signed test.A cohort of 316 children aged 1-18 years with SCA was evaluated with a male preponderance of 161 (57.4%). The mean age and age at diagnosis were 11.04 ± 5.56 and 4.2 ± 1.7 years, respectively. The prevalence of growth failure and short stature was 84.7%. The burden of GF was highest among post-pubertal participants (94.1%). The most important predictor of growth velocity deficit was age (R=0.045, standard coefficient = -0.22, =-03.51, p=0.001).The study demonstrated high prevalence of growth failure in children and adolescents with SCA which intensified with advancement in age and older age at diagnosis.

Authors & Co-authors:  Chikani Ugo Nnenna UN Bisi-Onyemaechi Adaobi A Ohuche Ijeoma I Onu Justus J Ugege Shalewa S Ogugua Chinwe C Mbanefo Ngozi N Chime Paschal P Emodi Ifeoma I

Study Outcome 

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Statistics
Citations :  Galadancia, N, Wudilb, BJ, Balogunc, TM, Ogunrinded, GO, Akinsuliee, A, Hasan-Hangaa, F, et al.. Current sickle cell disease management practices in Nigeria. Int Health 2014;6:23–8. https://doi.org/10.1093/inthealth/iht022.
Authors :  9
Identifiers
Doi : 10.1515/jpem-2021-0232
SSN : 2191-0251
Study Population
Male
Mesh Terms
Adolescent
Other Terms
BMI;growth failure;height velocity;sickle cell anemia (SCA)
Study Design
Longitudinal Study,Cohort Study,Cross Sectional Study
Study Approach
Country of Study
Niger
Publication Country
Germany