1996
DOI: 10.1007/bf02499894
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Polymorphisms of the interleukin-6 gene are associated with bone mineral density

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Cited by 41 publications
(48 citation statements)
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“…An increased frequency of an Xba I Restriction Fragment Length Polymorphism (RFLP, likelyto be due to 3' flanking region insertions, has been describedin some patients with SLE and elevated IL-6 levels [179]. Byusing polymerase chain reaction (PCR)-RFLP and sensitive polyacrylamide gel electrophoresis, an association between genotype for the 3' flanking region polymorphismand peak bone mineral density in women has been demonstrated [180]. Manipulating the genetic mechanismscontrolling the IL-6 levels and increasing the frequency of GG alleles in the population would prevent aging and age related diseases and be the key to eternal youth and immortality.…”
Section: Aging Age-related Disorders Interleukin-6 and Gene Therapymentioning
confidence: 99%
“…An increased frequency of an Xba I Restriction Fragment Length Polymorphism (RFLP, likelyto be due to 3' flanking region insertions, has been describedin some patients with SLE and elevated IL-6 levels [179]. Byusing polymerase chain reaction (PCR)-RFLP and sensitive polyacrylamide gel electrophoresis, an association between genotype for the 3' flanking region polymorphismand peak bone mineral density in women has been demonstrated [180]. Manipulating the genetic mechanismscontrolling the IL-6 levels and increasing the frequency of GG alleles in the population would prevent aging and age related diseases and be the key to eternal youth and immortality.…”
Section: Aging Age-related Disorders Interleukin-6 and Gene Therapymentioning
confidence: 99%
“…IL-6 influences osteoclast function and stimulates bone resorption. 19 Studies have found a link between polymorphisms in the IL-6 gene and BMD in otherwise healthy women 20 and in those with inflammatory bowel disease. 21 Collagen type 1a1 (COL1A1) gene mutations are responsible for the condition osteogenesis imperfecta.…”
mentioning
confidence: 99%
“…We are disappointed, however, that they have not mentioned a few earlier basic studies, viz., by Marcel Simon. In the late 1970s, Simon and his group (4,5) were the rst to show that HH was an autosomal recessive condition. In the ensuing 20 years several university groups searched for the hemochromatosis gene, and in 1996 it was found by a commercial rm (Mercator Genetics, Inc., Menlo Park, Calif., USA).…”
Section: High Prevalence Of Hemochromatosis In Nord-trøndelagmentioning
confidence: 99%
“…Finally, in ammatory cytokines lead to overproduction of nitric oxide, a potential mediator of bone loss that has been examined in arthritis but only to a limited extent in IBD (2). Polymorphisms in the IL-6 gene have been identi ed at the promoter region (-174 G/C) (3) and 3' untranslated region (variable nucleotide repeats) (4,5). These are linked to regulation of bone density by in uencing peak bone mass and resorption rate.…”
mentioning
confidence: 99%