Literature DB >> 8758125

Factors affecting prepubertal growth in homozygous sickle cell disease.

A Singhal1, J Morris, P Thomas, G Dover, D Higgs, G Serjeant.   

Abstract

OBJECTIVE: To investigate the role of haematological indices, socioeconomic status, and morbidity in prepubertal growth in homozygous sickle cell (SS) disease.
METHOD: Height, weight, and haematology were serially recorded in a cohort study of 315 children with SS disease from birth to 9 years at the sickle cell clinic of the University Hospital of the West Indies, Kingston, Jamaica.
RESULTS: Height increment between 3 and 9 years correlated positively with total haemoglobin at age 7 years in boys but not girls. Attained height and weight at age 7 years correlated positively with haemoglobin and fetal haemoglobin in boys but not girls. Only the correlation between haemoglobin and weight showed a significant gender difference. Partial correlation analysis suggested that the effect of haemoglobin was accounted for by the effect of fetal haemolglobin and further analysis indicated that height correlated with F reticulocyte count (a measure of fetal haemoglobin production) in both sexes but not with the ratio of F cells to F reticulocytes (a measure of F cell enrichment). Growth was not significantly related to mean red cell volume, proportional reticulocyte count, alpha thalassaemia, socioeconomic status, or morbidity.
CONCLUSION: A high concentration of fetal haemoglobin in boys with SS disease is associated with greater linear growth. It is postulated that in boys, low concentrations of fetal haemoglobin increase haemolysis and hence metabolic requirements for erythropoiesis, putting them at greater risk of poor growth. Differences in the relationship of haematology and growth between boys and girls with SS disease dictate that future analyses of growth take gender into account.

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Year:  1996        PMID: 8758125      PMCID: PMC1511554          DOI: 10.1136/adc.74.6.502

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  21 in total

1.  Individual variation in the production and survival of F cells in sickle-cell disease.

Authors:  G J Dover; S H Boyer; S Charache; K Heintzelman
Journal:  N Engl J Med       Date:  1978-12-28       Impact factor: 91.245

2.  Microscopic method for assaying F cell production: illustrative changes during infancy and in aplastic anemia.

Authors:  G J Dover; S H Boyer; W R Bell
Journal:  Blood       Date:  1978-10       Impact factor: 22.113

3.  Screening cord bloods for detection of sickle cell disease in Jamaica.

Authors:  B E Serjeant; M Forbes; L L Williams; G R Serjeant
Journal:  Clin Chem       Date:  1974-06       Impact factor: 8.327

4.  Delayed skeletal maturation in sickle cell anemia in Jamaica.

Authors:  G R Serjeant; M T Ashcroft
Journal:  Johns Hopkins Med J       Date:  1973-02

5.  Body habirus of Jamaican adults with sickle cell anemia.

Authors:  M T Ashcroft; G R Serjeant
Journal:  South Med J       Date:  1972-05       Impact factor: 0.954

6.  Haematological factors associated with proliferative retinopathy in homozygous sickle cell disease.

Authors:  R J Hayes; P I Condon; G R Serjeant
Journal:  Br J Ophthalmol       Date:  1981-01       Impact factor: 4.638

7.  Determinants of haemoglobin level in steady-state homozygous sickle cell disease.

Authors:  G Serjeant; B Serjeant; A Stephens; D Roper; D Higgs; M Beckford; J Cook; P Thomas
Journal:  Br J Haematol       Date:  1996-01       Impact factor: 6.998

8.  Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease.

Authors:  J M Topley; D W Rogers; M C Stevens; G R Serjeant
Journal:  Arch Dis Child       Date:  1981-10       Impact factor: 3.791

9.  Some social factors related to control of diabetes mellitus in adult Jamaican patients.

Authors:  S I Alleyne; E Y Morrison; R R Richards
Journal:  Diabetes Care       Date:  1979 Sep-Oct       Impact factor: 19.112

10.  Acceleration in linear growth after splenectomy for hypersplenism in homozygous sickle cell disease.

Authors:  A Singhal; P Thomas; T Kearney; S Venugopal; G Serjeant
Journal:  Arch Dis Child       Date:  1995-03       Impact factor: 3.791

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  9 in total

1.  Sickle cell disease and age at menarche in Jamaican girls: observations from a cohort study.

Authors:  G R Serjeant; A Singhal; I R Hambleton
Journal:  Arch Dis Child       Date:  2001-11       Impact factor: 3.791

2.  Brain volume in pediatric patients with sickle cell disease: evidence of volumetric growth delay?

Authors:  R Grant Steen; Temitope Emudianughe; Michael Hunte; John Glass; Shengjie Wu; Xiaoping Xiong; Wilburn E Reddick
Journal:  AJNR Am J Neuroradiol       Date:  2005-03       Impact factor: 3.825

3.  GDP versus ESHAP Regimen in Relapsed and/or Refractory Hodgkin lymphoma: A Comparison Study.

Authors:  Mani Ramzi; Aliraza Rezvani; Mehdi Dehghani
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2015-01-01

4.  Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State.

Authors:  Samuel Olufemi Akodu; Olisamedua Fidelis Njokanma; Omolara AdeoluKehinde
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2015-01-01

5.  Factors Associated with Growth Retardation in Children Suffering from Sickle Cell Anemia: First Report from Central Africa.

Authors:  Aimé Lukusa Kazadi; René Makuala Ngiyulu; Jean Lambert Gini-Ehungu; Jean Marie Mbuyi-Muamba; Michel Ntetani Aloni
Journal:  Anemia       Date:  2017-01-30

6.  Endocrine and metabolic complications in children and adolescents with Sickle Cell Disease: an Italian cohort study.

Authors:  V Mandese; E Bigi; P Bruzzi; G Palazzi; B Predieri; L Lucaccioni; M Cellini; L Iughetti
Journal:  BMC Pediatr       Date:  2019-02-11       Impact factor: 2.125

7.  SOCIOECONOMIC AND NUTRITIONAL CHARACTERISTICS OF CHILDREN AND ADOLESCENTS WITH SICKLE CELL ANEMIA: A SYSTEMATIC REVIEW.

Authors:  Amanda Cristina da Silva de Jesus; Tulio Konstantyner; Ianna Karolina Véras Lôbo; Josefina Aparecida Pellegrini Braga
Journal:  Rev Paul Pediatr       Date:  2018 Oct-Dec

8.  Association of sickle cell disease with anthropometric indices among under-five children: evidence from 2018 Nigeria Demographic and Health Survey.

Authors:  Mohammad Redwanul Islam; Md Moinuddin; Ayeda Ahmed; Syed Moshfiqur Rahman
Journal:  BMC Med       Date:  2021-01-15       Impact factor: 8.775

9.  Wasting and stunting are still prevalent in children with sickle cell anaemia in Lagos, Nigeria.

Authors:  Christopher I Esezobor; Patricia Akintan; Adebola Akinsulie; Edamisan Temiye; Titilope Adeyemo
Journal:  Ital J Pediatr       Date:  2016-05-04       Impact factor: 2.638

  9 in total

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