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R Deka

Publications and source records attributed to R Deka.

65 records · Page 4Linked to original sources
PubMed1988

Hemoglobin E distribution in ten endogamous population groups of Assam, India.

Previous studies have reported a high incidence of hemoglobin E (HbE) in Northeast Indian populations. In the present study 10 endogamous populations of Assam belonging to two racial groups, Caucasoid and Mongoloid, were examined. The frequency of HbE gene (Hb beta E) in the Caucasoid caste populations is around 0.1, whereas the gene is highly prevalent in the Mongoloid populations, frequencies ranging between 0.2 and 0.6. Predominance of Hb beta E in the Tibeto-Burman speakers is contrary to observations made in Southeast Asia, where an association between Austro-Asiatic speakers and high prevalence of HbE exist. The highest occurrence of the gene in this area, which is on the far end of the proposed centre of distribution in Northern Kampuchea and Northeast Thailand, is also a deviation from the expected pattern of gene distribution. It is speculated that Hb beta E in the Tibeto-Burman populations of Assam arose by an independent mutation which contributed to the high frequencies of Hb beta E in the Northeast Indian populations.

Asian People↗
PubMed1986

Investigations on the variability of haptoglobin, transferrin and Gc polymorphisms in Assam, India.

Ten different population groups of Assam - Brahmins, Kalitas, Kaibartas, Rajbanshis, Muslims, Ahoms, Chutias, Kacharis, Karbis and Sandwals - have been typed for haptoglobin and for transferrin (Tf) and Gc subtype polymorphisms. Tf and Gc allele subtype frequencies show a considerable inter-population heterogeneity. From genetic distance analysis it appears that the populations under study form some distinct clusters, which can be explained by the historical and ethnic affiliations of these populations. Especially the distribution of Gc subtype alleles reveals some Mongoloid admixture among Assamese populations, which is reflected by the presence of Gc1A8 alleles in them.

Gene Frequency↗
PubMed1985

Population study in Assam: ABO blood groups, haemoglobin E and G-6-PD deficiency.

An attempt has been made to give a comprehensive picture of occurrence of ABO blood groups, haemoglobin E and G-6-PD deficiency among certain representative populations of the two major racial groups--Mongoloids and Caucasoids--of Assam, India. The qualitative pattern of distribution of ABO gene frequencies shows a clear demarcation between these two major groups. The same is true in respect of HbE gene, too. The Mongoloids present high frequencies of this gene, while among the Caucasoids its frequency is comparatively much lower. With regard to G-6-PD deficiency the distinction between the two groups is not so clear cut, yet some Mongoloid populations show relatively higher incidence of the trait in comparison to that in the Caucasoid populations.

ABO Blood-Group System↗
PubMed1984

A genetic survey in four Mongoloid populations of the Garo Hills, India.

Four Mongoloid populations, viz., Garo , Hajong , Rabha and Koch, belonging to the Tibetoburman language family of Garo Hills, India, were examined for blood types ( A1A2BO , Rh, MN), secretor factor, ability to taste PTC and cerumen types. Gene A1 is more frequent than B in Hajong and Rabha . Garo shows a higher frequency of gene B, Koch also shows a little higher frequency of gene B than A. R1 is the commonest chromosome in all the groups followed by R2. Frequency of gene M is very high in all these populations. In respect of ABH secretion in saliva, there is preponderance of the secretor gene. Incidence of non- taster gene is somewhat lower in them. Dry cerumen gene is frequent in these Mongoloid groups. In general, the Garo Hills populations show closer affinity to the Mongoloids of Northeast India in respect of gene frequencies.

ABO Blood-Group System↗
PubMed1981

Fertility and haemoglobin genotypes: a population study in Upper Assam (India).

The Kachari in upper Assam, a Bodo tribe whose language belongs to the Tibeto-Burman family, have a 0.5 frequency of the haemoglobin E gene (Hb beta E), the highest prevalence of an abnormal haemoglobin gene so far reported. In view of this high prevalence, the reproductive performance of 200 Kachari couples with different Hb beta genotypes and the pre-reproductive mortality of their offspring were examined. The differences of relative fertility observed were very small and there was no differential mortality of children. These findings indicate that at present there is no selection at the haemoglobin beta-chain locus in the Kachari population.

Abortion, Spontaneous↗
PubMed1975

Predominance of the haemoglobin E gene in a Mongoloid population in Assam (India).

A high frequency of the haemoglobin E gene (HbbetaE) had been found in 1972 in the Ahom, a mongoloid population in Upper Assam. The present study confirms frequencies between 0.3 and 0.35 for this population in a larger sample from different areas. An even higher frequency near 0.5 was found in the Kachari of Upper Assam, a tribe of the tibetoburman Bodo group. HbbetaE frequencies in these groups are compared with the frequencies in the general Assamese population and the austroasiatic Khasi of Meghalaya.

Adolescent↗
PubMedDate not supplied

Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations.

We have analyzed the hypervariable locus D17S5 in four well-defined human populations (Kachari of Northeast India; Dogrib Indian of Canada; New Guinea Highlander of Papua New Guinea; and a relatively homogeneous Caucasian population of North German extraction) using both Southern blot analysis and the polymerase chain reaction (PCR) technique to: (1) compare the efficiency and limitation of Southern blotting versus PCR-based techniques in genotyping variable number of tandem repeat loci, and (2) provide allele frequency data at this locus in these four anthropologically defined populations. Preferential PCR amplification of smaller alleles associated with D17S5 was corrected by lowering the DNA template concentration to 200 ng, and by reducing the extension time to 2 min. A perfect correspondence was observed between the results from Southern blot and PCR analysis in all but one sample. A very large allele, of approximately 24 to 25 repeat units, detected by Southern blotting, could not be amplified by PCR, resulting in an incorrect genotyping rate of less than 0.5%. Considering the grave consequences of mistyping in forensic and paternity testing, it is suggested that heterozygous controls consisting of large and small alleles should be employed in each PCR experiment, and PCR-generated homozygotes should be confirmed by Southern blotting. Significant variation in the number and frequency of alleles at this locus was observed in the four examined populations. A total of 15 different alleles were detected. The average heterozygosity varied from 54% in the Dogrib to 89% in the Kachari. No heterozygote deficiency was observed at this locus in any of the examined populations.

Asian People↗
PubMedDate not supplied

Functional assessment of immune markers of graft rejection: a comprehensive study in live-related donor renal transplantation.

A better understanding of the immunobiological processes and predictors of graft rejection holds promise for the development of potential therapeutic strategies and also individualization of immunosuppression. The objective of this study is to analyze the clinical relevance of immune parameters such as antidonor antihuman leukocyte antigen (anti-HLA) antibodies, monitoring of cytokines and their receptors on the graft outcome following live-related donor renal transplantation. Flow cytometry-based methods were used to detect antidonor antibodies (flow cytometry crossmatch, FCXM) and intracellular cytokines. Enzyme-linked immunosorbent assay (ELISA) methods were employed to detect anti-HLA class I and class II antibodies and quantitative serum-soluble interleukin-2 receptor (sIL-2R) levels. The data revealed that patients with HLA class I-specific IgG antibody experienced higher acute rejection (AR) episodes at 1 yr in comparison to the antibody negative group (82% vs. 56%, p = 0.01). On the contrary, donor-specific class II antibodies (B+) did not have any influence on the graft survival. However, 15 recipients having both T- and B-cell antidonor antibodies (T+B+) had significantly poor graft survival (60%) as compared to the antibody-negative group (T-B-, 82%, p = 0.05). Additionally, patients having non-donor but HLA-specific antibodies (FCXM-/ELISA+) had poor graft survival as compared to the antibody-negative group (64% vs. 88%, p < 0.05). Further, patients undergoing AR episodes had significantly higher expression of IFN-gamma-producing T cells (19.16 +/- 7.4% median 17.50) as compared to their pre-transplant levels (5.68 +/- 1.63%, Median 5.20) and the non-rejecter group (5.97 +/- 4.39%, median 4.3, p = 0.0004). Similarly sIL-2 was significantly increased in AR episodes during the first month of transplantation (292 +/- 131.5 pmol/L) as compared to those with well-functioning grafts (p = 0.01) and healthy controls (p = 0.001). Evaluation of antidonor antibodies by flow cytometry is found to be relatively more sensitive and a better predictor of graft outcome. Further monitoring of cytokine expression profile of primed peripheral T-helper cells and quantitative analysis of sIL-2R offer additional valuable diagnostic and prognostic tools for follow-up of transplant subjects and a better alternative for functional assessment of immunosuppression.

Antibodies↗