Determinants of peak bone mineral density and bone area in young women

被引:58
作者
Ho, AYY [1 ]
Kung, AWC [1 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
关键词
peak bone mass; young women;
D O I
10.1007/s00774-005-0630-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoporosis is a disease caused by compromised bone strength, and individuals with a high peak bone mass at a young age are likely to have a high bone mass in old age. To identify the clinical determinants of peak bone mass in young adult women, 418 southern Chinese women, aged 20-39 years, were studied. Low bone mass was defined as areal bone mineral density (aBMD) Z-score < -1 at either the spine or total hip. Within the cohort, 62 (19.0%) and 86 (26.4%) women had low aBMD at the spine and hip, respectively. Regression model analysis revealed that low body weight (< 44 kg) was associated with an 8.3-fold (95% CI, 3.7-18.9) and a 6.8-fold (95% CI, 3.0-15.6) risk of having low aBMD at the spine and hip, respectively. Low body weight was also predictive of low volumetric BMD (vBMD) at the spine (odds ratio (OR) 7.8, 95% CI, 3.1-20.1) and femoral neck (OR 3.0, 95% CI, 1.3-7.1). A body height below 153 cm was associated with a 4.8-fold risk in the small L2-4 bone area (95% CI, 2.3-9.8) and a 3.9-fold risk in the small femoral neck area (95% CI, 1.9-8.1). Delayed puberty (onset of menstruation beyond 14 years) was associated with a 2.2-fold (95% CI, 1.0-4.9) increased risk of having low aBMD at the hip. Physical inactivity was associated with a 2.8-fold risk of low spine vBMD (OR 2.8, 95% CI, 1.1-6.7) and a 3.3-fold risk of low hip aBMD (95% CI, 1.0-10.0). Pregnancy protected against low spine aBMD (OR 0.4, 95% CI, 0.1-1.2) and spine vBMD (OR 0.1, 95% CI, 0.0-1.0), low femoral neck vBMD (OR 0.3, 95% CI, 0.1-1.1) and small L2-4 bone area vBMD (OR 0.3, 95% CI, 0.1-1.1). In conclusion, this study identified a number of modifiable determinants of low peak bone mass in young adult women. Maintaining an ideal body weight, engaging in an active lifestyle, and diagnosing late menarche may enable young women to maximize their peak bone mass and so reduce their risk of osteoporosis in later life.
引用
收藏
页码:470 / 475
页数:6
相关论文
共 36 条
[1]   Multiparity and bone mass [J].
Bererhi, H ;
Kolhoff, N ;
Constable, A ;
Nielsen, SP .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1996, 103 (08) :818-821
[2]   CRITICAL YEARS AND STAGES OF PUBERTY FOR SPINAL AND FEMORAL BONE MASS ACCUMULATION DURING ADOLESCENCE [J].
BONJOUR, JP ;
THEINTZ, G ;
BUCHS, B ;
SLOSMAN, D ;
RIZZOLI, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (03) :555-563
[3]  
CARTER DR, 1992, J BONE MINER RES, V7, P137
[4]  
DENT CE, 1973, CLIN ASPECTS METABOL, P1
[5]   Familial resemblance for bone mineral mass is expressed before puberty [J].
Ferrari, S ;
Rizzoli, R ;
Slosman, D ;
Bonjour, JP .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (02) :358-361
[6]   Emerging views about "osteoporosis", bone health, strength, fragility, and their determinants [J].
Frost, HM .
JOURNAL OF BONE AND MINERAL METABOLISM, 2002, 20 (06) :319-325
[7]   Peak bone mass [J].
Heaney, RP ;
Abrams, S ;
Dawson-Hughes, B ;
Looker, A ;
Marcus, R ;
Matkovic, V ;
Weaver, C .
OSTEOPOROSIS INTERNATIONAL, 2000, 11 (12) :985-1009
[8]   Attainment of peak bone mass at the lumbar spine, femoral neck and radius in men and women: relative contributions of bone size and volumetric bone mineral density [J].
Henry, YM ;
Fatayerji, D ;
Eastell, R .
OSTEOPOROSIS INTERNATIONAL, 2004, 15 (04) :263-273
[10]  
Hernandez CJ, 2003, OSTEOPOROSIS INT, V14, P843, DOI 10.1007/s00198-003-1454-8