Association between bone loss and promoter polymorphism in the IL-6 gene in elderly Japanese women with hip fracture

被引:13
作者
Feng, DY
Ishibashi, H
Yamamoto, S
Hosoi, T
Orimo, H
Machida, T
Koshihara, Y
机构
[1] Tokyo Metropolitan Inst Gerontol, Bone Res Grp, Itabashi Ku, Tokyo 1730015, Japan
[2] Saitama Univ, Fac Sci, Dept Regulat Biol, Saitama, Japan
[3] Tokyo Metropolitan Geriatr Hosp, Tokyo 173, Japan
关键词
IL-6; polymorphism; women; bone loss;
D O I
10.1007/s00774-003-0413-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recently, a G/C polymorphism was found at position -573 of the interleukin-6 (IL-6) gene promoter. We investigated how this genetic polymorphism relates to IL-6 production and osteoporosis in elderly Japanese women. Genomic DNA was extracted from an aliquot of monocytes in the bone marrow; the monocytes were simultaneously used to form osteoclast-like multinucleated cells (MNCs) and to produce IL-6. Of the 47 subjects with fractures, 96% had a C allele at position -573 of the IL-6 gene. Only 2 subjects possessed homozygotes of G at that position. We investigated IL-6 levels, MNC formation in bone marrow culture, and femoral neck bone mineral density (BMD) in the subjects with the GC and CC genotypes. There were no significant differences between these genotypes as regards IL-6 levels, MNC formation, and femoral neck BMD. However, in the CC genotype, there was a negative relationship between femoral neck BMD and IL-6 levels, and between femoral neck BMD and MNC formation, whereas in the GC genotype and combined (GC+CC) genotypes, femoral neck BMD tended to be related to IL-6 levels and MNC formation. Moreover, the stromal cells in the CC genotype showed higher IL-1alpha-stimulated IL-6 production than did the stromal cells in the GC genotype. Our findings suggest that important information might be obtained not only by continued comparison of different genotypes but also by comparative study within each particular genotype.
引用
收藏
页码:225 / 228
页数:4
相关论文
共 11 条
[1]  
Ferrari SL, 2000, J BONE MINER RES, V15, pS162
[2]   Interleukin 6 is autoregulated by transcriptional mechanisms in cultures of rat osteoblastic cells [J].
Franchimont, N ;
Rydziel, S ;
Canalis, E .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (07) :1797-1803
[3]   Genetic determination of bone density [J].
Greenfield, EM ;
Goldberg, VM .
LANCET, 1997, 350 (9087) :1263-1264
[4]   STRUCTURAL-ANALYSIS OF THE SEQUENCE CODING FOR AN INDUCIBLE 26-KDA PROTEIN IN HUMAN-FIBROBLASTS [J].
HAEGEMAN, G ;
CONTENT, J ;
VOLCKAERT, G ;
DERYNCK, R ;
TAVERNIER, J ;
FIERS, W .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 159 (03) :625-632
[5]   Practical guide for the use of bone mineral measurements in the assessment of treatment of osteoporosis: A position paper of the European Foundation for Osteoporosis and Bone Disease [J].
Kanis, JA ;
Devogelaer, JP ;
Gennari, C .
OSTEOPOROSIS INTERNATIONAL, 1996, 6 (03) :256-261
[6]   Reversibility of alendronate-induced contraction in human osteoclastlike cells formed from bone marrow cells in culture [J].
Koshihara, Y ;
Kodama, S ;
Ishibashi, H ;
Azuma, Y ;
Ohta, T ;
Karube, S .
JOURNAL OF BONE AND MINERAL METABOLISM, 1999, 17 (02) :98-107
[7]  
KURIHARA N, 1990, J IMMUNOL, V144, P4226
[8]   HOW MANY WOMEN HAVE OSTEOPOROSIS [J].
MELTON, LJ ;
CHRISCHILLES, EA ;
COOPER, C ;
LANE, AW ;
RIGGS, BL .
JOURNAL OF BONE AND MINERAL RESEARCH, 1992, 7 (09) :1005-1010
[9]   Fractures attributable to osteoporosis: Report from the National Osteoporosis Foundation [J].
Melton, LJ ;
Thamer, M ;
Ray, NF ;
Chan, JK ;
Chesnut, CH ;
Einhorn, TA ;
Johnston, CC ;
Raisz, LG ;
Silverman, SL ;
Siris, ES .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (01) :16-23
[10]   INCREASED INTERLEUKIN-6 PRODUCTION BY MURINE BONE-MARROW AND BONE-CELLS AFTER ESTROGEN WITHDRAWAL [J].
PASSERI, G ;
GIRASOLE, G ;
JILKA, RL ;
MANOLAGAS, SC .
ENDOCRINOLOGY, 1993, 133 (02) :822-828