scholarly journals Is protein intake associated with bone mineral density in young women?

2010 ◽  
Vol 24 (S1) ◽  
Author(s):  
Jeannette Michele Beasley ◽  
Laura E Ichikawa ◽  
Brett A. Ange ◽  
Leslie Spangler ◽  
Andrea Z LaCroix ◽  
...  
2010 ◽  
Vol 91 (5) ◽  
pp. 1311-1316 ◽  
Author(s):  
Jeannette M Beasley ◽  
Laura E Ichikawa ◽  
Brett A Ange ◽  
Leslie Spangler ◽  
Andrea Z LaCroix ◽  
...  

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.


1998 ◽  
Vol 68 (3) ◽  
pp. 749-754 ◽  
Author(s):  
D Teegarden ◽  
R M Lyle ◽  
G P McCabe ◽  
L D McCabe ◽  
W R Proulx ◽  
...  

2003 ◽  
Vol 35 (Supplement 1) ◽  
pp. S77
Author(s):  
L E. Miller ◽  
S M. Nickols-Richardson ◽  
D F. Wootten ◽  
L M. Pierson ◽  
W K. Ramp ◽  
...  

2011 ◽  
Vol 89 (3) ◽  
pp. 228-233 ◽  
Author(s):  
Gabriella Milos ◽  
Luigi M. Gallo ◽  
Branca Sosic ◽  
Daniel Uebelhart ◽  
Gerhard Goerres ◽  
...  

JAMA ◽  
1993 ◽  
Vol 270 (24) ◽  
pp. 2926-2927 ◽  
Author(s):  
R. R. Recker

Nutrients ◽  
2019 ◽  
Vol 12 (1) ◽  
pp. 21
Author(s):  
Katie Schraders ◽  
Giancarla Zatta ◽  
Marlena Kruger ◽  
Jane Coad ◽  
Janet Weber ◽  
...  

We would like to thank Moran and Sanchez Fernandez [...]


2013 ◽  
Vol 17 (11) ◽  
pp. 2570-2576 ◽  
Author(s):  
Shivani Sahni ◽  
Kerry E Broe ◽  
Katherine L Tucker ◽  
Robert R McLean ◽  
Douglas P Kiel ◽  
...  

AbstractObjectiveTo examine (i) the association of percentage of total energy intake from protein (protein intake %) with bone mineral density (BMD, g/cm2) and bone loss at the femoral neck, trochanter and lumbar spine (L2–L4) and (ii) Ca as an effect modifier.SettingThe Framingham Offspring Study.SubjectsMen (n 1280) and women (n 1639) completed an FFQ in 1992–1995 or 1995–1998 and underwent baseline BMD measurement by dual-energy X-ray absorptiometry in 1996–2000. Men (n 495) and women (n 680) had follow-up BMD measured in 2002–2005.DesignCohort study using multivariable regression to examine the association of protein intake % with each BMD, adjusting for covariates. Statistical interaction between protein intake % and Ca (total, dietary, supplemental) intake was examined.ResultsThe mean age at baseline was 61 (sd 9) years. In the cross-sectional analyses, protein intake % was positively associated with all BMD sites (P range: 0·02–0·04) in women but not in men. Significant interactions were observed with total Ca intake (<800 mg/d v. ≥800 mg/d) in women at all bone sites (P range: 0·002–0·02). Upon stratification, protein intake % was positively associated with all BMD sites (P range: 0·04–0·10) in women with low Ca intakes but not in those with high Ca intakes. In the longitudinal analyses, in men, higher protein intake % was associated with more bone loss at the trochanter (P = 0·01) while no associations were seen in women, regardless of Ca intake.ConclusionsThis suggests that greater protein intake benefits women especially those with lower Ca intakes. However, protein effects are not significant for short-term changes in bone density. Contrastingly, in men, higher protein intakes lead to greater bone loss at the trochanter. Longer follow-up is required to examine the impact of protein on bone loss.


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