Backgrounds and objectives:- Clinical presentation of sickle cell
disease (SCD) in India shows reduced episode of crisis and severity unlike
reported elsewhere. Sickle hemoglobin (HbS) polymerizes upon deoxygenation
causing RBC dehydration and consequently increases corpuscular hemoglobin
concentration which in turn accelerates more HbS polymerization precipitating
episodes of crisis. Any factor affecting reduced haemoglobin synthesis or
changes in low serum osmolality may affect disease outcome by altering cellular
hemoglobin concentration. The aim of this study was to elucidate the peculiar
disease presentation by evaluating hematological and blood electrolyte
alterations in the SCD patients from Chhattisgarh, central India. Methods:- For
the present study 100 SCD, 100 traits and 100 normal were selected from CG,
India. Genotypes were determined by Hb variant HPLC. Hematological and
biochemical test were performed using auto-analyzer. Results:- Mean MCV and
MCHC in SCD group was significantly lowered compared to control and trait.
Significant reduction of serum sodium and potassium level (125.6?3.4 and
3.2?0.86 mEq/l respectively) were observed in SCD group compared to control and
trait (137.4?3.25, 4?0.37 and 134.0?5, 3.7?0.84mEq/l respectively),
(p<0.001). Patients in stable and crisis state do not show any significant
difference in serum sodium and potassium level. Interpretation and Conclusion:-
Hyponatremia in the SCD study group might rehydrate RBC and could be an additional
contributing factor along with increase HbF response and co-existing microcytic
anaemia for fewer vaso-occlusive episodes in this geographical region.
Mechanism and significance of simultaneous Hyponatremia and hypokalaemia as
well hypochromic microcytic anaemia, the unusual finding in the SCD study
population, need to be elucidate further in future study. - See more at:
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