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Association of RANK gene variants with its circulatory level and bone mineral density in postmenopausal women with and without osteoporosis

By: Contributor(s): Description: pp1200-1209Subject(s): In: Current ScienceSummary: The present study aims to explore the possible association pattern of receptor activator of nuclear factor kappa B (RANK) gene variants (rs 35211496 and rs 1805034) with its circulatory level and bone mineral density (BMD) in North Indian postmenopausal women. In this case-control study, we recruited 165 postmenopausal osteoporotic women as cases (age 54.44 ± 6.00) and 165 healthy postmenopausal women as controls (age 54.47 ± 6.46). BMDs were taken in all subjects using dual energy X-ray absorptiometry at different skeletal sites, and genotyping was carried out using polymerase chain reaction and the restriction fragment length polymorphism method. RANK serum levels were also assessed in all enrolled subjects by enzyme-linked immunosorbent assay. Findings from the present study indicated that subjects with homozygous mutant TT genotype of rs35211496 (NC_000018.10 : g.62354528C > T) and rs1805034 (NC_000018.10 : g.62360008C > T) showed significantly low BMD at forearm, lumbar spine, hip and femoral neck and increased RANK level as compared to CC and CT genotypes. Furthermore, at rs1805034, a significant difference was noted in the frequency of RANK genotypes and alleles among osteoporotic cases and controls (P = 0.021; 0.005) respectively
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Item type Current library Vol info Status Barcode
Journal Article SNDT Juhu Available jp826.3
Periodicals SNDT Juhu Vol 128 No 12 Available JP826

The present study aims to explore the possible association pattern of receptor activator of nuclear factor kappa B (RANK) gene variants (rs 35211496 and
rs 1805034) with its circulatory level and bone mineral density (BMD) in North Indian postmenopausal
women. In this case-control study, we recruited 165
postmenopausal osteoporotic women as cases (age
54.44 ± 6.00) and 165 healthy postmenopausal women
as controls (age 54.47 ± 6.46). BMDs were taken in
all subjects using dual energy X-ray absorptiometry
at different skeletal sites, and genotyping was carried
out using polymerase chain reaction and the restriction fragment length polymorphism method. RANK
serum levels were also assessed in all enrolled subjects by enzyme-linked immunosorbent assay. Findings from the present study indicated that subjects
with homozygous mutant TT genotype of rs35211496
(NC_000018.10 : g.62354528C > T) and rs1805034
(NC_000018.10 : g.62360008C > T) showed significantly
low BMD at forearm, lumbar spine, hip and femoral
neck and increased RANK level as compared to CC
and CT genotypes. Furthermore, at rs1805034, a
significant difference was noted in the frequency
of RANK genotypes and alleles among osteoporotic
cases and controls (P = 0.021; 0.005) respectively

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