Literature DB >> 23284239

Resting blood lactate in individuals with sickle cell disease.

Jefferson Petto1, Jaqueline Brito de Jesus, Leila Monique Reis Vasques, Renata Leão Silva Pinheiro, Aila Mascarenhas Oliveira, Kelly Aparecida Borges Spinola, Wellington Dos Santos Silva.   

Abstract

BACKGROUND: The most common hereditary hemoglobin disorder, affecting 20 million individuals worldwide, is sickle cell disease. The vascular obstruction resulting from the sickling of cells in this disease can produce local hypoxemia, pain crises and infarction in several tissues, including the bones, spleen, kidneys and lungs.
OBJECTIVE: To determine red blood group genes in a Brazilian populations.
METHODS: The present study is characterized as a case control study, with the aim of identifying the baseline blood lactate concentration in individuals with hemoglobin SS and SC diseases. One-way ANOVA with the Tukey post-test was used to analyze the results and a p-value < 0.05 was considered significant. Calculations were made using the INSTAT statistical program. The graphs were generated using the ORING program. The study sample was composed of 31 men and women residing in the city of Santo Antônio de Jesus, Bahia, Brazil. The individuals were divided into two groups: Group GC of 16 subjects who did not present with any type of structural hemoglobinopathy; and Group GE composed of 15 individuals with ages between 2 and 35 years old, who had the SS and SC genotypes. Sample analyses were performed with 3 mL of blood during fasting.
RESULTS: The baseline blood lactate concentration of the SS and SC individuals was higher than that of the control group (p<0.001) with means of 4.86 ± 0.95; 3.30 ± 0.33; 1.31 ± 0.08 IU/L for SS, SC and controls, respectively. This corroborates the initial research hypothesis.
CONCLUSION: The baseline blood lactate of SS and SC individuals is 3 to 4 times higher than that of healthy subjects, probably due to the fact that these patients have a metabolic deviation to the anaerobic pathway.

Entities:  

Keywords:  Lactic acid; Physical exercise; Sickle cell anemia

Year:  2011        PMID: 23284239      PMCID: PMC3521431          DOI: 10.5581/1516-8484.20110010

Source DB:  PubMed          Journal:  Rev Bras Hematol Hemoter        ISSN: 1516-8484


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  2 in total

1.  Plasma metabolomics analysis in sickle cell disease patients with albuminuria - an exploratory study.

Authors:  Laila Elsherif; Wimal Pathmasiri; Susan McRitchie; David R Archer; Kenneth I Ataga
Journal:  Br J Haematol       Date:  2018-09-10       Impact factor: 6.998

2.  Physical activity level and performance in the six-minute walk test of children and adolescents with sickle cell anemia.

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Journal:  Rev Bras Hematol Hemoter       Date:  2017-03-31
  2 in total

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