The sickle cell trait (SCT) has been detected in approximately 300 million individuals worldwide. It has long been considered a benign carrier state providing relative protection against severe malaria [1]. However, clinical sequelae, such as exercise-related injury, renal complications, and venous thromboembolism, can occur in affected carriers [2]. Overall, evidence suggests that SCT may be neither a completely benign carrier state nor a true disease entity, but rather a risk factor for certain adverse outcomes that result from the interaction between genetic and environmental influences [3]. In the Basra governorate of southern Iraq, 6.48% of the population are carriers of the sickle hemoglobin (HbS) gene, giving a gene frequency of 0.0324 [4]. Another study in Dohuk in northern Iraq reported 1.2% carriers within the population of the concerned governorate [5].

Microcytic anemia is the most common form of anemia in children and adolescents. It represents a very heterogeneous group of diseases that may be either acquired (mostly due to iron deficiency) or inherited. Microcytic hypochromic anemia can result from a defect in globin genes (hemoglobinopathies or thalassemias), heme synthesis, or iron availability or acquisition by erythroid precursors [6]. Iron deficiency (ID) is the most common cause of anemia worldwide. However, iron deficiency anemia (IDA) is not distributed evenly across the world, exhibiting is a five-fold higher incidence in underdeveloped countries [7]. In 2011, the Southeast Asian, Eastern Mediterranean, and African regions of the WHO exhibited the lowest mean blood hemoglobin concentrations and the highest prevalence of anemia across population groups [8]. In Iraq, the prevalence of iron deficiency (ID) in children younger than five years of age is 14.4%, and the prevalence of IDA is 6.8% [9].

While the co-inheritance of another β-globin gene increases the proportion of HbS and therefore the risk of sickling, the combination with a deletion of an α-gene reduces intraerythrocytic HbS concentration, which consequently attenuates the problems due to SCT [10]. The co-inheritance of α⁺-thalassemia could reduce the effects of HbS on erythrocyte pathophysiology. The AS hemoglobin genotype likewise ameliorates both the reduced mean corpuscular volume (MCV) and mean corpuscular hemoglobin (MCH) values normally associated with the −α/−α genotype [11].

The present study was conducted to investigate the causes of microcytosis among children and adolescents with SCT in Basra and to evaluate selected hematological and biochemical variables in subjects with SCT and microcytosis.

Children and adolescents referred to the Center for Hereditary Blood Diseases (CHBD) at the Basra Maternity and Children's Hospital for suspected hemoglobinopathy were enrolled in this descriptive study lasting from 1st October 2015 through February 2016. A total of 95 symptomatic and asymptomatic children and adolescents, with ages ranging from 6 months to 18 years, were included in the study.

The total number of children and adolescents enrolled in this study was 95, and their ages ranged from 6 months to 18 years with a mean age of 6.04±4.46 years. Fifty-two (54.74%) of the children and adolescents in this study were ≤5 years of age, and the male to female ratio was 1.06. Most of these subjects lived in the Basra Center (69.47%), as illustrated in Table 1. Seventy-five (78.95%) of the studied subjects were symptomatic and referred to the CHBD for evaluation, and only 20 (21.05%) were asymptomatic and referred because of a positive family history of sickle cell disease. Pallor was the main symptom (44.21%), followed by bone pain (22.11%). Other causes of referral were bronchopneumonia (9.47%) and urinary tract infection (2.11%), as well as one case of left-sided weakness and repeated seizures.

A history of previous hospitalization was reported in 39 (41.05%) of the studied subjects, with infections occurring in 21 (22.10%) subjects, followed by 9 (9.47%) subjects being hospitalized for anemia. A total of 7 (7.37%) subjects had a previous history of blood transfusions (3 due to severe IDA, and 4 due to glucose-6-phosphate dehydrogenase (G6PD) deficiency). Four patients had surgery including tonsillectomy (two cases) and orthopedic causes (one case due to fracture, and the other due to avascular necrosis of the hip), as displayed in Table 1. The Hb concentrations in studied subjects ranged from 5.71 g/dL to 16.60 g/dL, and the MCV ranged from 45 fL to 94 fL, with 81 (85.26%) of the SCT subjects exhibiting low Hb concentrations compared to the values of healthy subjects of the same age and gender. Although the average values of Hb, MCV, MCH, and MCHC for all SCT subjects were lower than those of healthy individuals, no statistically significant difference in these variables was reported between symptomatic and asymptomatic subjects. This case was similar for other variables (RBC count, RDW-CV, WBC count, and platelet count); P>0.05. Among the 75 symptomatic SCT subjects, 64 (85.33%) had low MCV compared to 17 (85%) subjects with low MCV in the asymptomatic group, P>0.05 (Table 2).

Low MCV was reported in 81 (85.26%) subjects, while 12 (12.63%) subjects had normal MCV, and only 2 (2.05%) had high MCV. Out of the 49 male subjects with SCT, 47 (95.92%) of them had low MCV, and only 2 (4.08) had normal MCV. Out of a total of 46 female subjects with SCT, 34 (73.91%) of them had microcytosis, while 10 (21.74%) had normal MCV, and 2 (4.35%) had high MCV. The difference in MCV between the genders was statistically significant (P=0.006). The study also revealed that the average values of MCV, MCH, and S. ferritin were significantly lower in male subjects with SCT compared to female (P<0.05), while other hematological variables did not exhibit a significant difference between the genders, as illustrated in Table 3.

Children and adolescents with SCT and microcytosis had a significantly lower mean MCH and S. ferritin level (20.44±3.36 pg and 42.33±6.75 ng/mL, respectively) compared to those with normal MCV (24.60±1.48 pg and 73.28±23.59 ng/mL, respectively) and subjects with high MCV (29.30±1.69 pg and 217.30±164.90 ng/mL, respectively). The averages of the RBC count and RDW-CV were significantly higher in the microcytic group (4.83±0.85×10¹²/L and 14.25±2.38%, respectively) compared to those in the normocytic group (4.09±0.72×10¹²/L and 12.50±0.91%, respectively) and the macrocytic group (3.13±1.4110¹²/L and 12.90±1.41%, respectively); P<0.05. Multiple comparisons of the obtained averages using the Scheffé test showed that children and adolescents with microcytosis had a significantly higher RBC count (P=0.021) and RDW-CV (P=0.047) compared to those with normocytosis.

Out of the 81 subjects with microcytosis, 63 (77.78%) of them had ID, while the remaining 18 (22.22%) had normal iron status. Results of the capillary electrophoresis diagnosed one subject with Hb-Bart's disease and co-inheritance of α-thalassemia. Among subjects with SCT and normal MCV, 8 (66.67%) had ID, and 4 (33.33%) were not iron deficient. The distribution of iron status did not reveal significant changes in the frequency of MCV among those with or without ID (P>0.05), indicating that microcytosis was not related to ID alone. Among the subjects with ID, 36 (57.14%) were <5 years of age, 12 (19.05%) had a history of pica, 3 (4.76%) received blood, and 32 (50.80%) were receiving iron, folic acid, or both. In addition, 14 (22.22%) patients with SCT, microcytosis, and ID had low BMIZ (thin and severely thin). This study also revealed that in SCT individuals with microcytosis and ID, the average levels of S. ferritin and HbA2 were significantly lower, and the averages of RDW-CV, serum transferrin, and HbS were significantly higher in comparison to non-ID subjects; P<0.05, Table 4.

Correlation coefficients did not reveal a significant association between MCV and iron status in SCT subjects (P>0.05), Fig. 1. However, among the subjects with microcytosis, a different correlation pattern was discovered between MCV and iron status in ID (Fig. 2A) compared to the non-ID group (Fig. 2B).

This study assessed microcytosis in children and adolescents with SCT in Basra, southern Iraq, where the frequency of the disease is the highest in comparison with other Iraqi regions. The frequency of microcytosis was found to be high among SCT subjects, and although ID was reported in most of the cases, causes other than iron deficiency may have contributed to microcytosis in these subjects.

The mean Hb concentration in the study group was lower than that of healthy individuals, with no significant difference between symptomatic and asymptomatic SCT subjects and between male and female subjects. In the study of Obaid et al. in Basra, the mean Hb in healthy children with a comparable age (5.90 yr) was (11.50±0.99 g/dL) for male and (11.39±1.20 g/dL) for female subjects [17].

In the study of Chikhlikar and Wilkinson [18] the mean Hb in symptomatic SCT patients (7.71±2.11 g/dL) was significantly lower in comparison to that in asymptomatic subjects (12.98±2.02 g/dL).

Mustafa et al. [19] in Sudan reported that the blood profile in SCT subjects was comparable to that of healthy individuals, with a mean Hb of 12.50±1.98. The low Hb reported in this study can be explained by the increased demand for growth, repeated infections, and poor dietary habits of subjects.

The frequency of anemia in the present study was much higher than that reported in India by Patel et al. [20] (25%). This finding was expected, because most of the SCT subjects were referred to the center for evaluation and management due to different complaints including mainly pallor and infections.

The mean MCV obtained in this study was lower than the values reported for healthy individuals in Basra (86.35±5.72 fL for male and 87.09±5.94 fL for female subjects) [17] and in international data [1415]. This result is in agreement with the MCV reported by Patel et al. [20] (73.98 fL) among children, adolescents and adults with SCT and Mohanty et al. [21] (63.5±8.9 fL) in India. In contrast, the mean MCV was reported to be comparable to the values obtained in healthy individuals by Khan et al. [22] (89.4±8.7 fL) in India, El Ariss et al. [23] in Lebanon (84.3±7.6 fL).

In accordance with previous studies, MCVs were significantly lower in HbAS compared to HbAA participants. The effect of α⁺-thalassemia on the intra-erythrocytic concentration of HbS in HbAS subjects is well documented. Even in non-thalassemic HbAS subjects, the intra-erythrocytic concentration of HbS is lower than that of HbA, probably because of the greater affinity of α-globin for normal (β) compared to mutant (β^s) β-globin chains. However, the relative deficiency of α-globin chains in subjects with co-existent α⁺-thalassemia appears to intensify this effect so that, compared to those with both HbAS and α⁺-thalassemia, the intra-erythrocytic concentration of HbS is roughly halved in individuals with HbAS and −α/−α [11].

In this study, the mean MCV was significantly lower in males compared to that in females. In contrast, El Ariss et al. [23] reported a mean MCV in males of 84.7±7.4 fL, which was not significantly different from that in females (84.1±7.8 fL). Moreover, the present study reported a low MCH among subjects with SCT, which was found to be significantly lower in males than females. The same finding was reported by Patel et al. [20], where the mean MCH was low (22.32 pg). These differences can be explained by the possibly higher prevalence of α-thalassemia and IDA in Iraqi children and adolescents. In a national survey conducted in 2007, the prevalence of ID in Iraqi children aged 6 months to 14 years ranged from 50% to 70% [24]. The percentage of ID subjects with SCT was higher in this study than the national figures among the healthy population of the same age group.

The higher IDA among male subjects ≤5 years of age (54.74% of the studied SCT subjects) can be attributed to significant gender differences in Hb, MCV, ferritin, and transferrin receptors at infancy, suggesting a relative iron deficiency in boys. The gender differences in the abundance of Hb and transferrin receptors might reflect an increased risk for iron deficiency in boys, possibly because of gender differences in fetal iron accretion. However, for MCV, the remaining gender differences were independent of iron supplementation, growth variables, and complementary food intake, suggesting that other gender-related differences such as genetic or hormonal factors are responsible [25]. With regard to adolescents; significant differences between boys and girls in most eating habits and activity behaviors were reported, as boys were found to consume significantly more fast foods, sugar-sweetened drinks, and energy drinks than girls [26].

Although there are no data available concerning the prevalence of alpha thalassemia disorders in Iraq, the WHO reported that in Eastern Mediterranean regions, the frequency of these disorders constitutes 21.7% [27].

RBC distribution width-CV is significantly different between individuals with microcytosis and those with normal MCV. RDW-CV is known to be a sensitive and specific indicator of ID compared to other RBC indices [28]. In a study by Chikhlikar and Wilkinson [18] the mean RDW-CV was found to be 17.76±4.5% in symptomatic children and adolescents and 14.75±2.30% in asymptomatic subjects, while Patel et al. [20] reported a mean RDW-CV of 16.43%.

To distinguish microcytic SCT subjects with and without ID, the ratio of transferrin to logarithm ferritin fully separated those with serum ferritin <20 µg/L from the ones with ferritin >100 µg/L with a cut-off at 1.70. In the present study, most of the SCT subjects within the group of children younger than 5 years of age had microcytosis with ID, which is the age of increased metabolic demand [724]. The high frequency of ID in SCT subjects in Basra is in contrast with the results of Al-Harbi et al. [29] in Saudi Arabia, who did not report ID in SCT patients with microcytosis.

Individuals with microcytic SCT and without ID had lower HbS proportions (30.47±6.95%) compared to the 33.4±5.9% HbS proportion reported by Taha and Mansour [30] in Basra, which is also lower than the mean HbS in the present study sample (31.15±5.30%). Another finding of this study was the absence of a significant association between MCV and iron status, which implies that microcytosis is not relevant to ID. This would suggest the co-inheritance of one form of alpha-thalassemia variants.