Sickle cell disease is an autosomal recessive genetic disease linked to a genetic anomaly (E6V mutation, i.e. a substitution of adenine by Thymine) at the 6th codon of the short arm of chromosome 11. This genetic anomaly causes the formation of abnormal hemoglobin called Hemoglobin S having the characteristic of sickling red blood cells (the RBC takes the shape of a sickle) in the presence of certain conditions such as hypoxia, acidosis and fever [1] .

It is the most common “hemoglobinopathy” in Africa, with a prevalence of 20% in DR Congo. It constitutes a real public health problem since recent epidemiological data have shown that in the neonatal period, 2% of newborns are homozygous and approximately 40.000 births of children with sickle cell disease are estimated each year, while in the adult population, the Homozygous form affects approximately 2% of individuals [1] .

It is characterized by a hemolytic anemia with release of iron into the blood circulation, also with infectious and inflammatory episodes which can worsen following a deficiency of copper, zinc, serum iron, etc [2] - [4] . In addition to hemolysis, blood transfusion constitutes a source of iron intake in sickle cell patients. Indeed, each transfused erythrocyte concentrate provides approximately 200 mg of iron depending on its volume, thereby causing iron overload in polytransfused sickle cell patients [5] . However, the human body lacks a physiological mechanism for excreting this excess iron. Consequently, this excess iron accumulates and is responsible for cardiac, hepatic and endocrine damage making up a disease called hemochromatosis [6] .

The National Heart Lung and Blood Institute’s Sickle Cell Disease Management Guide has established a comprehensive program to monitor and treat iron overload. He also recommends screening for iron overload by analyzing serum ferritin levels from the start of transfusion therapy, and indicates that overload probably becomes detectable after twenty transfusions [7] .

In addition, homozygous sickle cell patients are exposed to iron deficiency following a nutritional deficiency during the growth period. As in developing countries, children, adolescents and pregnant women are particularly vulnerable [8] .

Depending on its role, copper transports iron in the body, contributes to the proper functioning of the immune system, etc.; High or low iron levels in the body can lower copper levels in adolescents, pregnant women and people with genetic diseases such as sickle cell anemia.

Indeed, several authors have reported that zinc deficiency is much more present during sickle cell disease and is associated with malnutrition which affects the immune system, thus exposing sickle cell patients to multiple infections [9] [10] .

This is why our study is based on the dosage of copper, zinc given their essential roles in the regeneration of red blood cells in the body, especially in sickle cell patients, and iron considered as a constituent element of hemoglobin [11] .

A study carried out on the contribution of soluble transferrin receptors in the evaluation of iron status during homozygous sickle cell disease revealed that 17.5% of sickle cell patients and 3.33% of controls (AA) had an increase in iron levels and the receptor transferrin, which demonstrated a severe iron deficiency in sickle cell patients [12] . Theoretically with hemolysis the plasma iron level should be higher.

Thus, it was a question of evaluating the plasma status of copper, zinc, iron (ferritin and transferrin) in the blood of sickle cell patients of all ages followed at the mixed medicine and sickle cell anemia center of Kinshasa (CMASS).

The interest of this study is to allow clinicians to provide the community as well as health professionals with useful information that can help them cope with and prevent vaso-occlusive crises (VOC) and thoracic acute syndrome (TAS).

It is an analytical—comparative study, the study concerned subjects with sickle cell disease and controls (non-sickle cell disease) followed at the Mixed Medicine and Sickle Cell Anemia Center in Kinshasa (CMMASS).

Included in the study, thirty polytransfused sickle cell subjects, not being in a state of severe vaso-occlusive crises, not having received a transfusion during the month and thirty non-sickle cell subjects were taken as controls, not recently having a transfusion. Free and informed consent was obtained, either from the subject himself for adults, or through the parent or guardian for children.

The sampling applied is of non-probabilistic convenience because the choice of patients was made according to their attendance at the center and concerned all subjects with homozygous sickle cell disease (SS) whose hemoglobin status was proven by the electrophoresis method of the Cellulose acetate hemoglobin.

The control group consisted of AA and AS people attending the same center and whose hemoglobin status was proven by electrophoresis.

The dosages of mineral elements included:

The parameters of the martial assessment included:

The following reference values were considered:

Statistical analysis:

To statistically process our results, we proceeded by calculating the average and the standard deviation as well as the calculated Z test.

All data were entered and analyzed using SPSS 15.0 software. The different variables were compared using the chi-square test, the averages were compared using the Student’s T-test. The significance threshold p retained was less than 0.05.

The sample consists of 60 patients including 30 sickle cell patients and 30 AA controls who consulted CMMASS/Yolo during the work period and who freely agreed to participate in the study. These results will be presented in the form of sociodemographic data and mineral element analysis results.

Mineral elements play an important role in the immune system in humans; their deficiency would favor certain biological variations, notably the occurrence of infections. However, our sickle cell patients are subject to multiple infections, hence the interest in the dosage of certain mineral elements in our study and the dosage of ferritin which is an iron storage protein for good guidance in the management of crises in sickle cell patients.

Our study consists of 60 patients including 30 sickle cell patients and 30 controls who consulted CMMASS/Yolo during the period of our study and who agreed to participate in it after informed consent. For the children, their parents freely agreed to have them participate.

The male gender is in the majority at 56.6% with a sex ratio of 1.30. This predominance is also found in other studies in the DR Congo [14] [15] . In Africa, other studies report the same observation [16] [17] . Finally, others see no predominance between the two sexes [18] [19] . This is the case of Thuilliez and Dreux. These differences would be related to the demographic data of each country because the transmission of sickle cell disease is not linked to sex.

The age of polytransfused sickle cell patients varies between 1 and 40 years. The average is 7.4 years for children and 27.4 for adults. These data seem to corroborate the study of Ilunga K. K. A. et al. [1] .

The study was limited to the dosages of three mineral elements among others: copper, iron and zinc and another parameter which is ferritin.

Regarding copper, out of 15 children with sickle cell disease, 4 children had abnormal cupraemia, including 2 with hypocupraemia < 12 µmol/l. 2 had hypercupremia and 11 had normal values. Compared to the 15 control children, 10 were within the normal range and 5 had hypocupremia. Concerning adults with sickle cell disease, 4 adults, 2 of whom had hypocupremia < 11 µmol/l and 2 others hypercupremia and 9 had normal values. Compared to the 15 adult controls, 2 presented hypocupremia, 1 hypercupremia and 12 had normal values. Copper deficiency can worsen anemia and neurological complications in a sickle cell patient, requiring regular monitoring and supplementation if necessary. And excess copper can lead to liver toxicities and other complications, requiring a reduction in copper intake [20] .

Copper is an anti-infectious and anti-allergic, it plays several roles in the body, among other things, it is essential for the production of melanin and stimulates the immune system while having an anti-inflammatory effect. In addition, this trace element contributes to strengthening the immune system and promotes healing and slows the development of bacteria and viruses [20] .

Based on the normal value of serum zinc, out of the 15 sickle cell patients evaluated, 10 subjects or 67% of sickle cell patients showed hypozincemia, 5 subjects or 33.3% presented normal zincemia; compared to children without sickle cell disease, 9 subjects or 60% have normal zincemia and 6 subjects or 40% have hypozincemia.

67% of sickle cell patients presented with hypozincemia and 33.3% were within the normal range. Unlike the control subjects, 10 had normal zincemia and 5 had hypozincemia. Zinc deficiency is linked to factors such as increased urinary zinc elimination and chronic intravascular hemolysis [21] [22] . A study confirms that there is a zinc deficiency which is a factor in malnutrition in sickle cell patients [23] .

There is also a close correlation between zinc deficiency and impaired immune functions. According to the literature, zinc is an essential trace element that is involved in numerous physiological functions and plays a role in the body’s immunity. A sufficient supply of zinc is therefore essential for better protection of sickle cell patients who are prone to multiple infections [20] [24] .

Comparing the results of sickle cell children and controls for serum iron, 60% of sickle cell children presented hyposideremia; Unlike the control children, 53.3% had hypersideremia and 13.3% had hyposideremia. A significant difference was found in children. Sickle cell patients presented a low level of serum iron compared to controls as shown in Table 3 . However, the diagnosis of iron deficiency in sickle cell subjects is not yet well established, due to the lack of specific tests to define their martial condition [25] . Iron deficiency was found in 17.5% of children with sickle cell disease and 20% presented hypersideremia, 3.33% hypersideremia was found in the control group [12] .

In adults, 33.3% with sickle cell disease presented hyposideremia, also 13.3% of control adults presented hyposideremia. On the other hand, 2 controls presented hypersideremia.

For transferrin in children, according to the analysis results, 4 sickle cell patients or 40% present hypotransferrinemia and 10% present hypertransferrinemia. Unlike the controls, 2 subjects or 20% presented hypertransferrinemia and 10% of children presented hypotransferrinemia.

In adults, 2 sickle cell subjects, or 20%, presented hyposideremia and 10% hypertransferrinemia, unlike in the controls, 4 adults, or 40%, presented hypersideremia and 10% hypotransferrinemia.

For the level of ferritinemia, 100% of subjects with sickle cell disease and controls have normal ferritinemia, compared to ironemia which increases in 53.3% of control children; and transferrinemia which decreases in 20% of control children and in 40% of children with sickle cell disease. In relation to sideremia, 20% of sickle cell patients presented hyposideremia in adults and 60% hyposideremia in children. 27% of adult controls presented hypersideremia. Thus, the hemochromatosis mentioned by the latter could not be confirmed by the ferritinemia which was normal for all subjects (100%), rather by the transferrinemia which decreased in the controls and increased in the sickle cell patients, which would mean an iron deficiency. The normal values of ferritinemia, with the hyposideremia of iron deficiency anemia, would be related to the disturbances linked to infection and inflammation [26] . Because of chronic hemolysis, which characterizes certain hemoglobinopathies such as sickle cell anemia and thalassemia, is not in itself a cause of iron overload [25] . These results illustrate the limits of the usual parameters in the diagnosis of mineral elements in sickle cell disease.

The reduction in transferrin, specific to hypersideremia, is only noted in 20% of controls, a phenomenon which could be explained by a reduction in its synthesis in favor of ferritin in the inflammatory context and its increase could reflect a tissue deficiency. In iron, no sign of infection or anemia was observed, especially since these receptors are considered an indicator of incipient tissue iron deficiency which has not yet caused anemia [27] - [29] and hyposideremia in 60% of children with sickle cell disease and 20% in adults, due to chronic hemolysis of sickle cell disease, would be at the origin of the correlation between hemoglobin and soluble receptors, since it results in a normal compensatory increase in erythropoietic activity to which the receptors are sensitive [30] .

To this end, patients with sickle cell disease should have regular assessments of their copper, zinc and iron levels to detect and treat deficiencies or excesses quickly depending on age and adapted to the specific needs of each patient.

This work focused on the evaluation of the plasma status of mineral elements such as copper, zinc and iron (ferritin and transferrin) in sickle cell patients. The study was carried out on 60 samples of mixed sex and age, including 30 sickle cell subjects and 30 control subjects followed at the SS mixed medicine and anemia center in Kinshasa.

Our results demonstrate not only the effective presence of hemochromatosis but also an iron deficiency in controls and in sickle cell patients, ignoring hemolysis; this leads us to say, despite the chronic hemolysis that sickle cell patients experience, ferritin is normally compared to other parameters where there have been significant variations following diet and sickle cell disease. Also the study reveals that sickle cell patients have copper and zinc deficiencies which can have harmful consequences on their health. These results highlight the importance of adequate screening and management of mineral deficiencies in sickle cell patients.

These observations show that sickle cell disease gives rise to multiple biological variations of which our studied parameters are one of them. This demonstrates the benefit of regular, effective medical monitoring leading not only to reducing crises but also to good care.

Thus, we suggest that sickle cell patients eat foods rich in mineral elements to avoid certain deficiencies which would lead to repeated crises.

In perception, this study can be continued on several parameters such as Hb, RBC, WBC, TfR, VGM and TCMH, CRP, stools to provide clinicians with a characteristic hematological and biochemical profile during sickle cell disease.