Adiponectin levels during steady state and vaso-occlusive crisis in Nigerian children with sickle cell anaemia

Sickle cell anaemia (SCA) is a chronic inflammatory hemoglobinopathy marked by recurrent vaso-occlusive crises (VOC) and end-organ damage. Adiponectin, an adipokine with anti-inflammatory and insulin-sensitizing properties, is well-studied in metabolic disorders but remains underexplored in SCA. This study assessed serum adiponectin levels in Nigerian children with SCA during steady state and VOC. We conducted a cross-sectional study involving 50 children with homozygous sickle cell genotype (HbSS) and 46 age- and sex-matched healthy controls with normal adult haemoglobin genotype (HbAA). Adiponectin levels were measured using ELISA, and group comparisons were performed. Multivariable linear regression was used to assess associations between adiponectin and clinical variables. Children with SCA had significantly higher adiponectin levels (median 3.2 µg/mL, IQR 2.20–4.38) compared to healthy controls (0.4 µg/mL, IQR 0.3–0.6; p<0.0001). Among the SCA group, those in VOC had higher adiponectin concentrations than those in steady state (median 4.00 µg/mL vs. 2.15 µg/mL; p<0.0001). These differences remained significant after adjusting for age, sex, BMI, and socio-economic status (p<0.001). Adiponectin levels are elevated in children with SCA, particularly during VOC, suggesting its potential role as a dynamic biomarker of disease activity. These findings contribute to understanding the inflammatory profile of paediatric SCA and support further research into adiponectin as a non-invasive marker in clinical monitoring.

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Journal
Annals of Hematology
Published
2026-03-23
DOI
https://doi.org/10.1007/s00277-026-06944-y
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
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article

Adiponectin levels during steady state and vaso-occlusive crisis in Nigerian children with sickle cell anaemia

Arinze Ejike Ulasi, Thomas Obiajulu Ulasi, Chisom Adaobi Nri-Ezedi, AN Ikefuna et al.
Annals of Hematology
Hemoglobinopathies and Related Disorders
article

Adiponectin levels during steady state and vaso-occlusive crisis in Nigerian children with sickle cell anaemia

Arinze Ejike Ulasi, Thomas Obiajulu Ulasi, Chisom Adaobi Nri-Ezedi, AN Ikefuna, Henry Chima Okpara
article en

Abstract

Sickle cell anaemia (SCA) is a chronic inflammatory hemoglobinopathy marked by recurrent vaso-occlusive crises (VOC) and end-organ damage. Adiponectin, an adipokine with anti-inflammatory and insulin-sensitizing properties, is well-studied in metabolic disorders but remains underexplored in SCA. This study assessed serum adiponectin levels in Nigerian children with SCA during steady state and VOC. We conducted a cross-sectional study involving 50 children with homozygous sickle cell genotype (HbSS) and 46 age- and sex-matched healthy controls with normal adult haemoglobin genotype (HbAA). Adiponectin levels were measured using ELISA, and group comparisons were performed. Multivariable linear regression was used to assess associations between adiponectin and clinical variables. Children with SCA had significantly higher adiponectin levels (median 3.2 µg/mL, IQR 2.20–4.38) compared to healthy controls (0.4 µg/mL, IQR 0.3–0.6; p<0.0001). Among the SCA group, those in VOC had higher adiponectin concentrations than those in steady state (median 4.00 µg/mL vs. 2.15 µg/mL; p<0.0001). These differences remained significant after adjusting for age, sex, BMI, and socio-economic status (p<0.001). Adiponectin levels are elevated in children with SCA, particularly during VOC, suggesting its potential role as a dynamic biomarker of disease activity. These findings contribute to understanding the inflammatory profile of paediatric SCA and support further research into adiponectin as a non-invasive marker in clinical monitoring.

Annals of HematologyVol. 105(4)
University of Nigeria (NG), Nnamdi Azikiwe University (NG), Nnamdi Azikiwe University Teaching Hospital (NG)
Openalex Percentile: Top 14%
Hemoglobinopathies and Related Disorders
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Adiponectin levels during steady state and vaso-occlusive crisis in Nigerian children with sickle cell anaemia — Arinze Ejike Ulasi, Thomas Obiajulu Ulasi, et al. · Annals of Hematology (2026) | TGRS Research Map | TGRS