scholarly journals Bone mineral density in Addison's disease: evidence for an effect of adrenal androgens on bone mass.

BMJ ◽  
1987 ◽  
Vol 294 (6575) ◽  
pp. 798-800 ◽  
Author(s):  
J P Devogelaer ◽  
J Crabbe ◽  
C Nagant de Deuxchaisnes
1999 ◽  
Vol 10 (6) ◽  
pp. 435-440 ◽  
Author(s):  
G. D. Braatvedt ◽  
M. Joyce ◽  
M. Evans ◽  
J. Clearwater ◽  
I. R. Reid

2003 ◽  
Vol 58 (5) ◽  
pp. 617-620 ◽  
Author(s):  
Esteban Jódar ◽  
María Pilar Ruiz Valdepeñas ◽  
Guillermo Martinez ◽  
Antonino Jara ◽  
Federico Hawkins

BMJ ◽  
1987 ◽  
Vol 295 (6591) ◽  
pp. 214-214 ◽  
Author(s):  
J P Devogelaer ◽  
J Crabbe ◽  
C Nagant de Deuxchaisnes

Bone ◽  
1993 ◽  
Vol 14 (4) ◽  
pp. 698-698
Author(s):  
M.P.Ruiz Valdepeñas ◽  
M.B.Lopez Alvarez ◽  
M.A. Valero ◽  
M. Leon ◽  
I. Breton ◽  
...  

Author(s):  
Hsin-Hua Chou ◽  
Sao-Lun Lu ◽  
Sen-Te Wang ◽  
Ting-Hsuan Huang ◽  
Sam Li-Sheng Chen

The association between osteoporosis and periodontal disease (PD) has been revealed by previous studies, but there have been few studies on the association in younger adults. We enrolled a total of 7298 adults aged 40 to 44 who underwent PD screening between 2003 and 2008. Data on quantitative ultrasound for the measurement of bone mineral density (BMD) were collected for the diagnostic criteria of osteopenia and osteoporosis. The Community Periodontal Index (CPI) was measured for defining PD. A multiple logistic regression model was used to assess the effect of low bone mass on the risk of PD. Of 7298 enrollees, 31% had periodontal pockets >3 mm, 36.2% had osteopenia, and 2.1% had osteoporosis. The 39.8% of PD prevalence was high in adults with osteoporosis, followed by 33.3% in osteopenia. A negative association was found between BMD and CPI value (p < 0.0001). Low bone mass was associated with the risk of PD (adjusted OR: 1.13; 95% CI:1.02–1.26) after adjusting the confounding factors, including age, gender, education level, overweight, smoking status, past history of osteoporosis, and diabetes mellitus. An association between BMD and PD among young adults was found. An intervention program for the prevention of PD and osteoporosis could be considered starting in young adults.


2012 ◽  
Vol 25 (3) ◽  
pp. 331-340 ◽  
Author(s):  
Susan Ziglar ◽  
Tracy S. Hunter

Maximizing bone mass in youth is touted as the best strategy to offset the natural losses of aging and the menopausal transition. Not achieving maximum peak bone mineral density (BMD) is an independent risk factor for osteoporosis and thus a public health concern. Adolescence is a critical time of bone mineralization mediated by endogenous estradiol. Research has shown that the highest velocity of bone mass accrual occurs 1 year before menarche and after the first 3 years. Low-peak attainment of BMD in young women is associated with contributing factors such as diets low in calcium, eating disorders, lack of exercise, smoking, and low estrogen states. Oral contraceptives (OCs) suppress endogenous estradiol production by suppressing the hypothalamic–pituitary–ovarian axis. Thus, OCs, by replacing endogenous estradiol with ethinyl estradiol (EE), establish and maintain new hormone levels. The early initiation and the use of very low dose of EE raises the possibility that bone mass accrual at a critical time of bone mineralization in young women or adolescents may be jeopardized. This review examines the studies of BMD in adolescents and young women that use combination hormonal contraception. Some studies had inherent limitations, such as small trial, poor control of confounders, failure to exclude women with prior use of hormonal contraceptives, or prior pregnancy from control groups. The vast majority of reviewed studies showed OCs containing 20 to 30 µg of EE interfere with acquisition of peak BMD. Limited numbers of studies examine the effects of OCs containing 35 µg on adolescents and young adults. Additionally, studies are needed evaluating the progestin component of OCs as their differing androgenic properties may affect bone mineralization as well.


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