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Indian Journal of Medical Sciences, Vol. 59, No. 2, February, 2005, pp. 51-56 Original Article G6PD deficiency in Vataliya prajapati community settled in Surat Gupte Snehalata C., Patel Pratima U., Ranat Jasmine M. Surat Raktadan Kendra and Research Centre, B/h. T. and T. V. Middle School, Gopipura, Surat - 395 001 Code Number: ms05009 Abstract BACKGROUND: A Study on Vataliya Prajapati was published earlier but heterozygous females were not identified.AIMS: To compare incidence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in random and unrelated subjects, present and previous study and as per their original habitat. Incidence of heterozygous deficiency and clinical implication of deficiency was also determined. SETTINGS AND DESIGN: Camps were organized in Katargaon and Amroli regions. Blood specimens, with relevant demographic information, were collected from those who attended the camp. METHODS AND MATERIAL: A total of 1644 random blood samples were collected from 404 families participating in the camps. Nitroblue tetrazolium dye test was used for G6PD deficiency screening and quantitative assay for measurement of G6PD enzyme activity. STATISTICAL ANALYSIS USED: χ2 test was used to evaluate significance and mean values were compared by the Student's "t" test. RESULTS: Incidence of G6PD deficiency was found as 22% among all the random samples tested. However, the G6PD deficiency among unrelated members was 27.9% in males and 12.4% (P<0.001,df 1). The 13.9% of the females with heterozygous G6PD deficient status, together with the homozygous deficient phenotype makes the incidence comparable with males. Incidence of deficiency was comparable with previous study, in Katargam and Amroli and in Amerli and Bhavganar districts. Deficient subjects had mild anemia and hemolytic crisis rarely occurred. CONCLUSION: Vataliya Prajapatis have high incidence of G6PD deficiency without severe chronic hemolytic anemia. However before prescribing medicines physician should know the G6PD status of a Vataliya Prajapati patient. KEYWORDS: G6PD deficiency, Vataliya Prajapati, G6PD enzyme activity, Hemolytic crisis, Chronic hemolytic anemia INTRODUCTION Surat has about 20,000 inhabitants of Vataliya Prajapati community. They have high prevalence of red cell Glucose-6-phosphate dehydrogenase (G6PD) enzyme deficiency. Previous study at our institute, reported 29.8% incidence in them.[1] Molecular genetic studies have revealed the mutation present as G6PD Mediterranean.[2] G6PD deficient subjects can have chronic hemolytic anemia or hemolytic crisis developing after consumption of certain drugs.[3],[4] The screening test for G6PD deficiency, which is based on a qualitative assay, can easily identify the defect among males but in females, by virtue of its X-linked inheritance, reliable results could only be obtained by quantitative assay. However the G6PD enzyme levels in normal males and females are same as in female G6PD gene on one X chromosome is inactive.[5] Since in previous study quantitative assay was not performed to detect the heterozygous status for G6PD deficiency in females, the present study was undertaken to address this aspect. Attempt is also made to study the incidence in Katargam and Amroli; in families having different surnames and as per their native district. Hemoglobin levels will be analyzed to assess the degree of anemia in them and information about their medical history will be evaluated to assess the clinical implication of G6PD deficiency in them. MATERIALS AND METHODS After getting Institutional ethical committee′s clearance for the project in August 1999, it was planned to investigate about 10% population of Vataliya Prajapati community in Surat after getting their informed consent. In consultation with the community leader, camps were organized during the period September 1999 to June 2004 (In previous study the sample collection was from 1996 to February 1998) in Amroli and Katargam areas of Surat City, where majority of the members of the Vataliya Prajapati community resides. Information regarding sex, age, family name, native place (village, taluka and district), history of neonatal jaundice, hemolytic crisis or drug induced hemolytic anemia and any other past and present illness etc were recorded through the personal interview conducted. Usually the whole family attended the camp. Separate records were kept about the relationships between the family members. An analysis based on unrelated samples, siblings and children were excluded from the counting. Blood Samples were collected from 1644 subjects in EDTA bulbs. Hematological parameters were measured using an automatic hematology analyzer (Nihon Khoden) as per the manufacturer′s instructions. Qualitative G6PD deficiency screening was carried out by Nitroblue Tetrazolium (NBT) dye test.[6] Blood was incubated with glucose6-phosphate, nicotinamide adenine dinucleotide phosphate (NADP), NBT dye and phenazine methasulphate. The G6PD enzyme if present, converts NADP to NADPH, which will cause the soluble NBT dye to be reduced to insoluble formazan particles in presence of phenozine metasulphate. Thus normal individual shows a dark brown precipitate within 30 minutes. Deficient subjects or heterozygous females show little or no change or a tan color. Samples from females and deficient males were subjected to quantitative assay.[7] In this assay conversion of NADP to NADPH per minute is measured on UV spectophotometer. One mole of glucose-6-phosthate can reduce one mole of NADP. Statistical analysis Statistical significance was evaluated by χ2 test using 2x2 table and mean values were compared by the Student′s "t" test.[8] RESULTS A total 12 camps- six in Katargam, five in Amroli and one at our institute
were organized. Four hundred and four families had attended these camps and
1644 blood
samples were collected at random. Of these, the G6PD deficiency was detected
in 359 (22%). Out of 985 males 275 (27.9%) and of 659 females
84 (12.2%)
were G6PD deficient. The incidence significantly differed in males and females
( χ2= 53.2, degree of freedom (df) =1, P = <0.001).
The data on distribution for G6PD deficiency among various families revealed that in slightly over the half of the families (numbering 211 or 52.2%) both the parents had normal G6PD while remaining 193 families (47.8%) had the defective G6PD gene. Further break-up showed that in 28 families (6.9%), both the parents were G6PD deficient whereas in 22 families (5.4%), the father was deficient with the mother being heterozygous deficient. In remaining families, only one parent had the deficient gene. Analysis of the samples collected in two regions of Surat did not show statistically significant difference in the incidence of G6PD deficiency (χ2= 0.17, df =1, P > 0.5) as the Vataliya Prajapati residents of Amroli showed incidence of 21.4% (166 out of 776) and those of Katargam 22.2% (193 out of 868). It was revealed that all the Vataliya Prajapati subjects were originated
from two adjacent districts Amreli or Bhavnagar in the Saurashtra region of
Gujarat
State. Majority of them were from Rajula or Khambha Taluka of Amreli or Mahuva
Taluka of Bhavnagar. [Table - 2] displays
the incidence of G6PD deficiency amongst the subjects with their origin in
Amreli and Bhavnagar districts. G6PD deficiency rate was slightly higher in
Amreli with no statistical significance (χ2 = 0.4 , df =1, P = 0. 5)
for males and for female (χ2 = 0.09, df =1, P = 0.75). It is however
note worthy that information on the native place could not be reliably recorded
for all the subjects with the result, the sample size was too small to make
any inference. DISCUSSION In India, incidence of G6PD deficiency has been reported as 0 to 37% in
different castes and communities.[9],[10] The present study substantiates the observation made earlier.[1] As
expected both the studies have reported significantly higher incidence of G6PD
deficiency in males compared to females because of the sex-linked inheritance.
The comparison of the incidence observed among males in the present and previous
study reveals that previous study has slightly higher incidence, while it reported
lower incidence for females. However, the difference was statistically insignificant.
These observations could be attributed to the fact that previous study had
used Dichlorophenol-indophenol dye decolorization test for screening, while
we have used a different NBT test. Secondly the G6PD activity was not measured
in females. Present study reported 24.2% incidence G6PD deficiency among unrelated males and 12.7% among females. The 13.9% of
the females with heterozygous G6PD deficient status, together with the homozygous
deficient phenotype makes the incidence comparable with males. ACKNOWLEDGEMENT Authors are grateful to Vataliya Prajapati community leaders particularly Shri Kishor Pandav and Shri Gordhan Pandav who helped us in organizing the camps. Because of them it was possible to get the co-operation of this community.References
Copyright 2005 - Indian Journal of Medical Sciences The following images related to this document are available:Photo images[ms05009t1.jpg] [ms05009t3.jpg] [ms05009t2.jpg] |
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