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The status of health and medicine in the Middle East - disease control


Histopathological relationship between severity of inflammatory reaction in gastritis and intensity of Helicobacter pylori in the antrum

Hypospadias: does the usage of Clomiphene citrate influence the incidence

Level of Hemoglobins in Sickle Cell Trait in Basrah using HPLC


Assure Safer Drug Therapy in the Middle East


An Investigation of Medical staff awareness of patients’ rights in Fasa hospitals and Medical centers

The investigation of effective factors on patients’ satisfaction Parent-Adolescent Relationships in the City of Amol


An epidemiological survey on maternal mortality rate and fatcors contributing to maternal mortality in rural area of Peshawar



Microdilution In Vitro Susceptibility Testing of 71 species of Dermatophytes isolated from pediatric cases in Nigeria against five antifungal agents


Development of Encounter Forms for Cardiovascular Disease Risk Management

 


Abdulrazak Abyad
MD, MPH, MBA, AGSF, AFCHSE

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Level of Hemoglobin in Sickle Cell Trait in Basrah Using HPLC

 
AUTHOR

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.


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.

Key words: sickle, trait, hemoglobin S.

INTRODUCTION

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.

 

 

 

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.

METHODS

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.

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% (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%.

DISCUSSION

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.

 

Table 1. Levels of hemoglobin S and F among 647 patients.

  Males (248) Females (363) Total (647)
Hemoglobin S mean ±SD 33.5±5.5 33.4±6.2 33.4±5.9
Hemoglobin Fmean ±SD 1.5±1.5 1.4±2.8 1.5±2.3

Table 2. Different levels of hemoglobin S.

Hemoglobin S (%) Males n (%) Females n (%) Total n (%)
<20% 3 (1.0) 8 (2.2) 11 (1.7)
20-30 62 (21.8) 88 (24.2) 150 (23.1)
31-40 205 (72.1) 244 (67.2) 449 (69.3)
>40 14 (4.9) 23 (6.3) 37 (5.7)
Total n (%) 284 (100) 363 (100) 647 (100)
N denotes number.

REFERENCES
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2. Al-kasab F M, Al-lusi F A, Adnani M S, Al-kafajei A M B .The prevalence of sickle cell disease in Abu-Al-Khasib district of Southern Iraq. J Tropical Med Hygiene 1981;84:77-80.
3. Mohammed AM, Hili FM, Nadkarni KV, Bhagwat GP, Bapat JP.Hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in hospital births in Bahrain. Ann Saud Med 1992;12:536-539.
4. Hamdi IM , Kamakshi KS, Ghani EA. Pregnancy outcome in women with sickle cell trait. Saudi Med J . 2002; 23 : 1455-1457.
5. Ajayi AA.Should the sickle cell trait be reclassified as a disease state. European Journal of Internal Medicine 2005; 16:463.
6. Tyagi S, Choudhry PV, Saxena R. Subclassification of HbS syndrome:is it necessary? Clin Lab Haem 2003: 25;377-381.
7. Head CE, Conroy M, Jarvis M, Phelan L, Bain BJ. Some observations on the measurement of haemoglobin A2 and S percentages by high performance liquid chromatography in the presence and absence of a thalassaemia . J Clin Pathol 2004;57:276-280.
 
8. International committee for standarisation in hematology. Recommendation for neonatal screening for hemogloinopathies.J Clin Lab Hematol 1988;10:335-345.
9. Al-Shawi TS .A study of sickle cell disease in young adult males in Iraq.A thesis submitted to the college of medicine ,university of Baghdad 1988 :p68.
10. Al-Shakour A A , Al-Suhail A A. Percentage of HbS among cases of sickle-cell trait in Basra, Iraq. Eastern Mediterranean Health Journal .2000 ; 6: 233-237.
11. Al-Awamy BH. Obeservation on the clinical features of sickle cell disease in early childhood. Saudi Med J 1999 ;20:277-282.
12. Reid HL, Famodu AA. Spectrophotometric quantitation of haemoglobin fraction in heterzygous sickle-cell trait . Medical laboratory sciences, 1988, 45:143-145.
13. Smith JA, Natta CL. The percentage of haemoglobin-S in individuals with sickle-cell trait. Blood. 1981; 58 (suppl. 1):64a.
14. Bilto YY ,Assaf M SH. Prevalence of hemoglobinopathies in central region of Jordan. Association of Arab universities Journal of medical sciences 1998;1:17-24.