Fetal Hemoglobin Modifies the Disease Manifestation of Severe Plasmodium Falciparum Malaria in Adult Patients with Sickle Cell Anemia

نویسندگان

  • Prasanta Purohit
  • Siris Patel
  • Pradeep Kumar Mohanty
  • Padmalaya Das
  • Jogeswar Panigrahi
چکیده

hemoglobin modifies the disease manifestation of severe Plasmodium falciparum malaria in adult patients with sickle cell anemia. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by-nc/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Sickle cell anemia (SCA) and Plasmodium falciparum malaria are two major public health problems in the state of Odisha, India. The prevalence of sickle cell gene in the western part of Odisha is 13.1%, 1 P. falciparum contributes 23% of cases and 15% of malaria-related deaths in India. Various African studies have shown that, even though SCA protects from P. falciparum infection, the risk of severe illness and death due to malaria is higher. 2,3 Though several factors are responsible for the disease severity in P.falciparum malaria in patients with SCA, it was recently found that fetal hemoglobin (HbF), a physiological hemoglobin usually found higher in patients with SCA had a negative epistatic interaction with HbS during protection against malaria. 4 The role of HbF against P. falciparum malaria in cases with normal hemoglobin genotypes has been widely studied and found to be protective against severe disease manifestation. So it is necessary to investigate this association in the regions with high prevalence of sickle cell gene and high endemicity of P. falciparum malaria. This study aims to find out the effect of HbF level on the clinical manifestation of severe P.falciparum malaria in patients with SCA. Forty-six adult patients with SCA along with severe P. falciparum malaria admitted in the Department of Medicine of this institute were included in this study. The mean age of patients was 25.4±8.8 years (range, 17 to 60 years) with 58.7% (27/46) being males. The hemoglobin variants including HbF was estimated by Cation-Exchange high performance liquid chromatography (CE-HPLC) using Variant II – í µí»½-thalassemia short program (Bio-Rad laboratories, Hercules). The mean % HbF level was found to be 18. 2 ± 4.9 %; ranging from 6.0 to 29.0 %. The severity of malaria was defined by WHO guideline in 2010. 5 The severity due to the malarial infection was defined by the presence of single or multiple complications. Cerebral malaria, severe malarial anemia, jaundice, acute renal failure and/or hepatopathy were considered as the major clinical symptoms of the patients. Among the various clinical symptoms, the incidence of cerebral malaria was 37.0% (17/46) followed by …

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

C1 Inhibitor, C3 Activator, IgG, IgA, and IgM Titers in Nigerian Sickle Cell Disease Patients with Plasmodium falciparum

Background: Sickle cell disease (HbSS) is a major health problem in Nigeria and ma-laria has been implicated as a leading cause of morbidity/mortality in sickle cell disease patients. Few reasons were put forward to explain the observed morbidity/mortality of HbSS subjects due to Plasmodium falciparum (P. falciparum) malaria. Objectives: To determine the level of immunoglobulin classes (IgM, Ig...

متن کامل

The Influence of Fetal Hemoglobin on Clinical and Hematological Variables of Children and Adolescents with Sickle Cell Anemia in Basra, Southern Iraq

Background: There are many parameters that modulate the severity of sickle cell anemia. Fetal hemoglobin (Hb F) is one of these major variables. However, its effect is clinically inconsistent. We conducted a descriptive study to assess the influence of Hb F on clinical events and hematological variables in patients with sickle cell anemia. Methods: 151 patients with sickle cell anemia with a st...

متن کامل

Natural protection against severe Plasmodium falciparum malaria due to impaired rosette formation.

Genes for two lethal diseases, thalassemia and sickle cell anemia, are favored by evolution because, in their heterozygous form, they protect against cerebral malaria. Rosette formation, the binding of uninfected red cells (RBCs) to Plasmodium falciparum-infected RBCs (PRBCs), has previously been found to be associated with cerebral malaria, the most important severe manifestation of P falcipar...

متن کامل

Parasitemia and Hematological Alterations in Malaria: A Study from the Highly Affected Zones

Background& Objectives: Inspite of intensive worldwide efforts to reduce its transmission, malaria remains the most serious and widespread protozoal infection of humans. It is a protozoan disease transmitted by the bite of infected female anopheles mosquito. Malaria has long featured prominently in the grey area between parasitology and hematology. This study has been...

متن کامل

Side Effects of Hydroxyurea in Patients with Sickle Cell Anemia

Background: Hemoglobin S arises is the result of a point mutation (A-T) in the sixth codon on the -globin gene on chromosome 11 causing sickle cell anemia. The presence of fetal hemoglobin in infancy plays a relatively protective role for vaso-occlusive symptoms that are the major contributor for the morbidity and mortality among patients with sickle cell anemia. hydroxyurea, an s-phase-specif...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2016