Abstract

SummaryAreal bone mineral density (aBMD) predicts future fracture risk. This study explores associations between use of tobacco and bone accretion in Norwegian adolescents. Our results indicate that use of snuff is negatively associated with accretion of aBMD in adolescence and may be a signal of increased future fracture risk.PurposeBone mineral accrual in childhood and adolescence is a long-term primary preventive strategy of osteoporosis. Areal bone mineral density (aBMD) is a surrogate measure of bone strength and a predictor of fracture risk. The aim of this population-based 2-year follow-up cohort study was to explore associations between use of snuff and smoking and changes (∆) in aBMD in Norwegian girls and boys aged 15–17 years at baseline.MethodsThe first wave of the Tromsø study, Fit Futures was conducted from 2010 to 2011. Femoral neck (FN), total hip (TH), and total body (TB) bone mineral content (BMC) and aBMD were measured by dual-energy X-ray absorptiometry. Information on use of snuff, smoking habits, and other lifestyle related variables were collected through self-administered questionnaires. Two years later, during 2012–2013, the measurements were repeated in the second wave. The present study included 349 girls and 281 boys and compared “non-users” (n = 243 girls, 184 boys) with “users” (n = 105 girls, 96 boys) of snuff and “non-smokers” (n = 327 girls, 249 boys) with “smokers” (n = 21 girls, 31 boys) using linear regression adjusted for age, baseline height and weight, change in height and weight, pubertal maturation, physical activity, ethnicity, alcohol consumption, diagnosis known to affect bone, and medication known to affect bone. The influence of “double use” on bone accretion was also explored.ResultsIn girls, no associations between use of snuff and ∆aBMD were found. In boys, use of snuff was associated with reduced bone accretion in all ∆aBMD models. Sensitivity analysis with exclusion of “sometimes” users of snuff strengthened associations at femoral sites in girls and attenuated all associations in boys. In girls, no associations between smoking and ∆aBMD were found. In boys, only the association with TB ∆aBMD was significant in the fully adjusted models. In girls, “double users” analyses showed similar association to smoking. In boys, nearly all models showed statistically significant associations with a difference of ~ 1–2% in ∆aBMD between “non-users” and “double users” during 2 years of follow-up.ConclusionsOur results indicate that tobacco use in late adolescence could be detrimental to bone accretion and may be a signal of increased fracture risk in adult life.

Highlights

  • Osteoporosis and its clinical manifestation, fragility fractures, constitute major public health challenges worldwide, and Norway has one of the highest reported hip fracture incidences in the world [1, 2]

  • Negative associations between use of snuff and ΔaBMD were observed at all skeletal sites

  • Our findings suggest an inverse association between use of snuff and Areal bone mineral density (aBMD) changes in late adolescence

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Summary

Introduction

Osteoporosis and its clinical manifestation, fragility fractures, constitute major public health challenges worldwide, and Norway has one of the highest reported hip fracture incidences in the world [1, 2]. Bone mineral levels in the elderly is a result of peak bone mass (PBM) achieved during childhood and adolescence and subsequent age-related bone loss [4]. Adolescence is a critical period for building bone as bone accrual peaks around the age of 12.5 among girls and 14 years of age for boys and roughly 95% of total adult bone mass is accrued within 4 years following the peak [5, 6]. Optimizing the genetic potential of PBM in adolescence is a long-term primary preventive strategy of osteoporosis. Around 20–40% of PBM achievement is attributed to lifestyle choices, and several modifiable behavioral determinants such as physical activity, body composition, and use of recreational drugs have been identified [7]. Tobacco use has been associated with lower aBMD during bone-building years [8, 9]

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