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Afr Health Sci ; 18(4): 1003-1009, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30766566

ABSTRACT

BACKGROUND: Sickle cell disease is characterized by chronic complications that affect almost all body organs. Pancreatic disease is rare in SCD. CA 19-9 is a non-specific surrogate marker for pancreatic disease especially carcinoma. CA 19-9 levels have not been evaluated in SCD patients in our environment. OBJECTIVES: The study aimed to compare the levels of CA 19-9 in homozygous sickle cell disease subjects in steady state with those of (Hb AS) and normal healthy subjects (Hb AA). METHOD: Seventy nine subjects including 39 Hb SS, 19 Hb AS and 21 Hb AA subjects were recruited in a cross-sectional study in Nnamdi Azikiwe University and Teaching Hospital. Haemoglobin genotype and CA 19-9 estimation were done using Hb electrophoresis and enzyme linked immunosorbent assay respectively. Data was analyzed with IBM SPSS 21. P value was set at 0.05. RESULT: The mean CA 19-9 (U/ml) level in Hb SS, Hb AS and Hb AA were 13.6 ± 7.6, 15.3 ± 9.9, and 20.0 ± 15.9 respectively. [Reference value <37U/ml] CA 19-9 was significantly lower in Hb SS compared to Hb AA subjects (p = 0.035). CONCLUSION: Low levels of CA 19-9 in Hb SS may suggest reduced pancreatic disorders in SCA.


Subject(s)
Anemia, Sickle Cell/blood , CA-19-9 Antigen/blood , Hemoglobin A , Hemoglobin, Sickle , Adolescent , Adult , Age Factors , Cross-Sectional Studies , Female , Genotype , Hospitals, University , Humans , Male , Nigeria , Severity of Illness Index , Sex Factors , Young Adult
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