Jenan Yassien Taha MD,
Department of Pathology and Forensic
Medicine,
Basrah College of Medicine
Abbas Ali Mansour MD,
Department of Medicine,
Basrah College of Medicine.
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ABSTRACT
Background: Sickle-cell
trait (SCT) is the heterozygous state
of the sickle cell gene. The aim of
this study is to give hemoglobin S(HbS)
level in SCT in Basrah (Southern Iraq),
which is the discriminating test for
diagnosis.
Methods: This
was a cross sectional hospital based
study for patients with sickling disorder
who attended the hematology center
for screening. The total number of
patients was 647, of them 248 were
males and 363 were females.
Results: Mean
±SD of HbS for males was 33.5±5.5%
versus 33.4±6.2 % for females, and
for both sexes 33.4±5.9%. In most
of the patients (69.3%), the HbS range
was 31-40 %. Only 5.7% of patients
had HbS >40%.
Conclusion: We,
for the first time, reported the level
of HbS among both sexes with SCT in
Basrah. cares.
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Key words: sickle,
trait, hemoglobin S.
Sickle-cell trait (SCT) is
the heterozygous state of the sickle cell
gene.[1] The prevalence of sickle cell disease
reaches up to 16% of the population in the
South of Iraq.[2] Reported incidence of
SCT in Bahrain is about 11% ,3 and among
Omani women is 9.1%.[4]
SCT contrary to common beliefs
is not always a benign condition.[4] It
has been associated with increased mortality
during physical exertion in athletes and
non-athletes, reduced exercise tolerance
during long-distance running, increased
coronary risk and coronary bypass graft
surgery, heightened risk of renal carcinoma,
thrombo-embolism and death during prolonged
air flight, and a 10-fold increase in the
risk of hemorrhagic stroke.[5] Differentiating
this condition from other sickle syndromes
is mandatory to take certain precautions
during surgical procedures and other stressful
situations, to detect rare but important
complications.
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The use of high-performance
liquid chromatography (HPLC), which facilitates
quantification of the various haemoglobin
types, may help in subclassification of
the sickle syndrome and make diagnosis of
SCT easier.[6]
The aim of this study is to
give hemoglobin S (HbS) levels in SCT in
Basrah (Southern Iraq), which is the discriminating
test for diagnosis.
This was a cross sectional
hospital based study for patients with sickling
disorder who attended the hematology center
for screening. From each patient 5 ml of
blood was taken in an EDTA tube and the
test performedwithin 3-4 days, in the teaching
hospital in Basrah. Patient samples were
studied by HPLC on a Bio-Rad Variant 2 instrument
(Bio-Rad Laboratories, Hemel Hempstead,
Hertfordshire) to do quantitative assessment
of haemoglobins F, A, A2, and S. The study
was done in the years 2000-2005.
A diagnosis of SCT was made
if patients had both haemoglobin A and HbS,
with the proportion of haemoglobin A being
greater than that of HbS. [7,8]
The total number of patients
was 647, of them 248 were males and 363
were females.
Mean ±SD of HbS for males
was 33.5±5.5% versus 33.4±6.2 % for females,
and for both sexes 33.4±5.9% (Table 1).
While for hemoglobin F for males was 1.5±1.5%
versus 1.4±2.8% for females, and for both
sexes 1.5±2.3%. In most of patients (69.3%),
the HbS range 31-40 %(Table 2). Only 5.7%
of patients were having HbS >40%.
Mean level of HbS in our study
for both sexes was 33.4±5.9 % among SCT
.In Iraqi,Al-Shawi TS , found mean ±SD of
HbS to be 34±6.2 in males with SCT in a
study of army recruits .9 Previous study
from Basrah concentrated on a trimodal distribution
of the amounts of HbS, but no exact range
value was given.10 In general the level
of HbS in SCT ranges from 20-50%11 with
a mean value of 38 ± 5 %.12,13In Jordan,
the HbS level among SCT was 39.8± 3.8%.14
In conclusion: we for the first time reported
the level of HbS among both sexes with SCT
in Basrah.
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