Inclusion of tobacco exposure as a predictive factor for decreased bone mineral content

被引:43
作者
Benson, BW
Shulman, JD
机构
[1] Texas A&M Univ, Div Radiol,Baylor Coll Dent, Dept Diagnost Sci, TAMUSHSC, Dallas, TX 75246 USA
[2] Texas A&M Univ, Baylor Coll Dent, Dept Publ Hlth Sci, TAMUSHSC, Dallas, TX 75246 USA
关键词
D O I
10.1080/14622200500259119
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Tobacco exposure has been implicated as a risk factor for decreased bone density, which might result in osteoporosis. Cotinine, a metabolite of nicotine, is commonly used as a marker for tobacco exposure (active or passive). The objective of the present study was to compare tobacco exposure with other predictive factors for low bone mineral content (BMC), as determined by dual photon bone absorptiometry (DXA) in a national U.S. sample. Publicly available interview and clinical examination data from the Third National Health and Nutrition Examination Survey, 1988-1994 (NHANES-III) were used. Our data included 14,060 subjects from 19,528 randomly selected representative U.S. households. Clinical laboratory data included serum values for calcium and cotinine. BMC was assessed radiologically by DXA at five proximal femur sites. BMC values were adjusted for age, as well as height, weight, and bone area to correct for bone and body size. We used t tests to compare continuous variables and chi-square tests to explore associations between categorical variables. Multivariate regression models were developed for each gender with appropriate covariates. Intertrochanter BMC explained the most variation (highest R-2) and was selected as the basis of the comparison. Serum cotinine had a significant inverse relationship to BMC in both males (p=.0069) and females (p=.0063). Serum cotinine, as a marker for tobacco exposure, is a statistically significant risk factor for decreased BMC in both genders and should be included in multivariate regression models to predict low BMC.
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页码:719 / 724
页数:6
相关论文
共 34 条
[11]   Differences in bone mineral density, bone mineral content, and bone areal size in fracturing and non-fracturing women, and their interrelationships at the spine and hip [J].
Deng, HW ;
Xu, FH ;
Davies, KM ;
Heaney, R ;
Recker, RR .
JOURNAL OF BONE AND MINERAL METABOLISM, 2002, 20 (06) :358-366
[12]  
DeSantis Anthony, 2002, Expert Opin Pharmacother, V3, P835
[13]   EFFECTS OF NICOTINE ON CELLULAR FUNCTION IN UMR 106-01 OSTEOBLAST-LIKE CELLS [J].
FANG, MA ;
FROST, PJ ;
IIDAKLEIN, A ;
HAHN, TJ .
BONE, 1991, 12 (04) :283-286
[14]   COMPARISON OF AREAL AND ESTIMATED VOLUMETRIC BONE-MINERAL DENSITY VALUES BETWEEN OLDER MEN AND WOMEN [J].
FAULKNER, RA ;
MCCULLOCH, RG ;
FYKE, SL ;
DECOTEAU, WE ;
MCKAY, HA ;
BAILEY, DA ;
HOUSTON, CS ;
WILKINSON, AA .
OSTEOPOROSIS INTERNATIONAL, 1995, 5 (04) :271-275
[15]   FACTORS ASSOCIATED WITH STRESS-FRACTURE IN YOUNG ARMY WOMEN - INDICATIONS FOR FURTHER RESEARCH [J].
FRIEDL, KE ;
PATIENCE, TH ;
NUOVO, JA ;
DETTORI, JR .
MILITARY MEDICINE, 1992, 157 (07) :334-338
[16]  
Gunter E.W., 1996, LAB PROCEDURES USED
[17]   Risk factors for longitudinal bone loss in elderly men and women: The Framingham Osteoporosis Study [J].
Hannan, MT ;
Felson, DT ;
Dawson-Hughes, B ;
Tucker, KL ;
Cupples, LA ;
Wilson, PWF ;
Kiel, DP .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (04) :710-720
[18]  
Hollinger JO, 1999, J BIOMED MATER RES, V45, P294
[19]   Risk factors for osteoporosis in men [J].
Izumotani, K ;
Hagiwara, S ;
Izumotani, T ;
Miki, T ;
Morii, H ;
Nishizawa, Y .
JOURNAL OF BONE AND MINERAL METABOLISM, 2003, 21 (02) :86-90
[20]   SMOKERS HAVE LESS DENSE BONES AND FEWER TEETH [J].
JOHNSTON, JD .
JOURNAL OF THE ROYAL SOCIETY OF HEALTH, 1994, 114 (05) :265-267