Genetic variant of lactase-persistent C/T-13910 is associated with bone fractures in very old age

被引:34
作者
Enattah, NS
Sulkava, R
Halonen, P
Kontula, K
Järvelä, I
机构
[1] Univ Helsinki, Cent Hosp, Lab Serv, Mol Genet Lab, FIN-00290 Helsinki, Finland
[2] Univ Helsinki, Dept Med Genet, Helsinki, Finland
[3] Univ Helsinki, Dept Med, Helsinki, Finland
[4] Natl Publ Hlth Inst, Dept Mol Med, Helsinki, Finland
[5] Univ Kuopio, Dept Publ Hlth & Gen Practice, FIN-70211 Kuopio, Finland
[6] Univ Kuopio, Ctr Informat Technol, FIN-70211 Kuopio, Finland
[7] Rheumatism Fdn Hosp, SF-18120 Heinola, Finland
关键词
adult-type hypolactasia; single-nucleotide polymorphism (SNP); bone fractures; elderly people;
D O I
10.1111/j.1532-5415.2005.53014.x
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
OBJECTIVES: To determine the relation between the C/T-13910 single-nucleotide polymorphism residing 13,910 base pairs from the 5' end of the lactase gene associated with lactase persistence and the occurrence of bone fractures in elderly people. DESIGN: Population-based study. SETTING: Vantaa 85+ population-based study, including all 601 subjects born before April 1, 1906, who were living in the city of Vantaa, Finland, on April 1, 1991. PARTICIPANTS: Four hundred eighty-three people aged 85 and older (106 men and 377 women). MEASUREMENTS: Genotype determination was made using a polymerase chain reaction minisequencing technique. RESULTS: The frequency of the genotype C/C-13910 associated with adult-type hypolactasia (low lactase enzyme activity or primary lactose malabsorption (LM)) was significantly greater in individuals with hip fractures, with an adjusted odds ratio (OR) of 3.7 (95% confidence interval (CI)=1.8-7.8), wrist fractures with an adjusted OR of 2.5 (95% CI=1.2-5.2), and hip and wrist fractures combined with an adjusted OR of 4.1 (95% CI=2.0-8.3). CONCLUSION: The C/C-13910 genotype associated with primary LM could represent a genetic risk factor for bone fractures for elderly people.
引用
收藏
页码:79 / 82
页数:4
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