Smoking is associated with impaired bone mass development in young adult men: A 5‐year longitudinal study

It has previously been shown that smoking is associated with reduced bone mass and increased fracture risk, but no longitudinal studies have been published investigating altered smoking behavior at the time of bone mass acquisition. The aim of this study was to investigate the development of bone density and geometry according to alterations in smoking behavior in a 5‐year, longitudinal, population‐based study of 833 young men, age 18 to 20 years (baseline). Furthermore, we aimed to examine the cross‐sectional, associations between current smoking and parameters of trabecular microarchitecture of the radius and tibia, using high‐resolution peripheral quantitative computed tomography (HR‐pQCT), in young men aged 23 to 25 years (5‐year follow‐up). Men who had started to smoke since baseline had considerably smaller increases in areal bone mineral density (aBMD) at the total body (mean ± SD, 0.020 ± 0.047 mg/cm2 versus 0.043 ± 0.040 mg/cm2, p < 0.01) and lumbar spine (0.027 ± 0.062 mg/cm2 versus 0.052 ± 0.065 mg/cm2, p = 0.04), and substantially greater decreases in aBMD at the total hip (−0.055 ± 0.058 mg/cm2 versus −0.021 ± 0.062 mg/cm2, p < 0.01) and femoral neck (−0.077 ± 0.059 mg/cm2 versus −0.042 ± 0.070 mg/cm2, p < 0.01) than men who were nonsmokers at both the baseline and follow‐up visits. At the tibia, subjects who had started to smoke had a smaller increment of the cortical cross‐sectional area (CSA) than nonsmokers (8.1 ± 4.3 mm2 versus 11.5 ± 8.9 mm2, p = 0.03), and a larger decrement of trabecular volumetric BMD (vBMD) than nonsmokers (−13.9 ± 20.5 mg/mm3 versus −4.1 ± 13.9 mg/mm3, p < 0.001). In the cross‐sectional analysis at follow‐up (23–25 years of age), smokers had significantly lower trabecular vBMD at the tibia (7.0%, p < 0.01) due to reduced trabecular thickness (8.9%, p < 0.001), as assessed using HR‐pQCT, than nonsmokers. In conclusion, this study is the first to report that men who start to smoke in young adulthood have poorer development of their aBMD at clinically important sites such as the spine and hip than nonsmokers, possibly due to augmented loss of trabecular density and impaired growth of cortical cross‐sectional area. © 2012 American Society for Bone and Mineral Research.

[1]  D. Mellström,et al.  Increased physical Activity is Associated With Enhanced Development of Peak Bone Mass in Men: A Five-year Longitudinal study , 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[2]  D. Bailey,et al.  Bone mineral accrual from 8 to 30 years of age: An estimation of peak bone mass , 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[3]  D. Mellström,et al.  Cortical consolidation due to increased mineralization and endosteal contraction in young adult men: a five-year longitudinal study. , 2011, The Journal of clinical endocrinology and metabolism.

[4]  A. Tenenhouse,et al.  Peak bone mass from longitudinal data: Implications for the prevalence, pathophysiology, and diagnosis of osteoporosis , 2010, Journal of Bone and Mineral Research.

[5]  D. Mellström,et al.  Association of physical activity with trabecular microstructure and cortical bone at distal tibia and radius in young adult men. , 2010, The Journal of clinical endocrinology and metabolism.

[6]  D. Mellström,et al.  Trabecular volumetric bone mineral density is associated with previous fracture during childhood and adolescence in males: The GOOD study , 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[7]  J. Kaufman,et al.  Early smoking is associated with peak bone mass and prevalent fractures in young, healthy men , 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[8]  I. Redlund‐Johnell,et al.  Smoking predicts incident fractures in elderly men: Mr OS Sweden , 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[9]  M. Iki,et al.  Smoking among premenopausal women is associated with increased risk of low bone status: the JPOS Study , 2010, Journal of Bone and Mineral Metabolism.

[10]  J. Cauley,et al.  Correlates of Trabecular and Cortical Volumetric BMD in Men of African Ancestry , 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[11]  Bjarni V. Halldórsson,et al.  Impact of Genetics on Low Bone Mass in Adults , 2008, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[12]  R. Eastell,et al.  Risk Factors for Vertebral and Nonvertebral Fracture Over 10 Years: A Population‐Based Study in Women , 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[13]  Steven K Boyd,et al.  Load distribution and the predictive power of morphological indices in the distal radius and tibia by high resolution peripheral quantitative computed tomography. , 2007, Bone.

[14]  D. Mellström,et al.  Smoking is associated with lower bone mineral density and reduced cortical thickness in young men. , 2007, The Journal of clinical endocrinology and metabolism.

[15]  R. Klesges,et al.  A meta-analysis of the effects of cigarette smoking on bone mineral density , 2001, Calcified Tissue International.

[16]  D. Mellström,et al.  Age of Attainment of Peak Bone Mass Is Site Specific in Swedish Men—The GOOD Study , 2005, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[17]  C. Slemenda,et al.  The contribution of bone loss to postmenopausal osteoporosis , 1990, Osteoporosis International.

[18]  H. Kroger,et al.  Smoking and fracture risk: a meta-analysis , 2005, Osteoporosis International.

[19]  P. Vestergaard,et al.  Fracture risk associated with smoking: a meta‐analysis , 2003, Journal of internal medicine.

[20]  G. S. Beaupré,et al.  A theoretical analysis of the relative influences of peak BMD, age-related bone loss and menopause on the development of osteoporosis , 2003, Osteoporosis International.

[21]  W. Mechelen,et al.  Validation of a physical activity questionnaire to measure the effect of mechanical strain on bone mass. , 2002, Bone.

[22]  J. Strain,et al.  The Effect of Nutrient Intake on Bone Mineral Status in Young Adults: The Northern Ireland Young Hearts Project , 2002, Calcified Tissue International.

[23]  L. Melton,et al.  Relationship of serum sex steroid levels to longitudinal changes in bone density in young versus elderly men. , 2001, The Journal of clinical endocrinology and metabolism.

[24]  D. Reid,et al.  Osteoporosis and its management. , 1999, Hospital medicine.

[25]  R. Rizzoli,et al.  Determinants of Peak Bone Mass and Mechanisms of Bone Loss , 1999, Osteoporosis International.

[26]  P. Rüegsegger,et al.  In vivo high resolution 3D-QCT of the human forearm. , 1998, Technology and health care : official journal of the European Society for Engineering and Medicine.

[27]  M. Law,et al.  A meta-analysis of cigarette smoking, bone mineral density and risk of hip fracture: recognition of a major effect , 1997, BMJ.

[28]  N. Ortego-Centeno,et al.  Effect of Tobacco Consumption on Bone Mineral Density in Healthy Young Males , 1997, Calcified Tissue International.

[29]  J. Eisman,et al.  Genetic influences on bone turnover, bone density and fracture. , 1995, European journal of endocrinology.

[30]  J. Palmgren,et al.  Exercise, smoking, and calcium intake during adolescence and early adulthood as determinants of peak bone mass , 1994, BMJ.

[31]  S. Cummings,et al.  The accuracy of self-report of fractures in elderly women: evidence from a prospective study. , 1992, American journal of epidemiology.

[32]  R B Mazess,et al.  Bone density in premenopausal women: effects of age, dietary intake, physical activity, smoking, and birth-control pills. , 1991, The American journal of clinical nutrition.

[33]  J. Hopper,et al.  Genetic determinants of bone mass in adults. A twin study. , 1987, The Journal of clinical investigation.