HOW CAN WE PROTECT PEAK BONE MASS AND FUTURE BONE HEALTH FOR ADOLESCENT WOMEN? - BY SUPPORTING OVULATION AND AVOIDING COMBINED HORMONAL CONTRACEPTION USE
Prior, J. C. (2017). How can we protect peak bone mass and future bone health for adolescent women? - By supporting ovulation and avoiding combined hormonal contraception use. Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo, 35(2), 121-124. https://doi.org/10.1590/1984-0462/;2017;35;2;00019
Prior JC. How can we protect peak bone mass and future bone health for adolescent women? - By supporting ovulation and avoiding combined hormonal contraception use. Rev Paul Pediatr. 2017;35(2):121-124. doi:10.1590/1984-0462/;2017;35;2;00019
Prior, J. C. "How can we protect peak bone mass and future bone health for adolescent women? - By supporting ovulation and avoiding combined hormonal contraception use." Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo, vol. 35, no. 2, 2017, pp. 121-124.
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RRM Academy Synopsis
Ovulation Patterns Linked to Bone Health in Teen Girls
This paper reviews studies on ovulation, birth control, and bone growth in teen girls. The review looks at a small study, a pooled analysis, and an unpublished analysis of about 900 girls. Skipped ovulation and combined hormonal birth control both link to smaller bone gains in teens.
Key Findings
A pooled analysis of women from their teens through their 30s linked more ovulation-disturbed cycles to almost 1% more spinal bone loss per year (-0.86%/year, 95% CI -1.68 to -0.04, p=0.04).
In a small study of 13 teen girls, ovulation began at least 10 months after the first period, and its timing tracked with whole-body bone gains.
A pooled analysis of about 900 girls ages 12 to 19 found combined hormonal contraceptive users had greater two-year spinal bone loss than non-users (-0.02 g/cm2, 95% CI -0.03 to -0.01, p=0.0007).
In a trial of women ages 20 to 35 with menstrual cycle disturbances, cyclic progestin therapy raised spinal bone density about 2% a year, versus a 2% yearly loss with placebo.
Interpretation
This is an editorial. The author reviews past research and argues for a view. Her evidence includes one very small study of 13 girls, one pooled analysis, and one analysis not yet reviewed by other scientists. Most studies she cites show a link. They do not prove causation. The only controlled trial used a different drug, studied grown women, and did not test cyclic progesterone or include teens. The author says a trial comparing cyclic progesterone with combined hormonal birth control in teens has not been done yet.
RRM Context
Restorative reproductive medicine treats teen cycle problems, like cramps or heavy flow, as clues to study. Charting a cycle can show if ovulation is happening. This paper says that matters for bone health as well as fertility. The author's caution about combined hormonal birth control in teens fits RRM's habit of looking for the pattern behind a hard cycle. She says the pill covers up the problem and leaves the cause unresolved.
Our editorial summary of this paper, not the article's abstract.
Guthardt Y et al., 2026·Sci Rep·Free full text on PubMed Central
This systematic review and meta-analysis examined the relationship between menstrual cycle phases and the incidence of muscle injuries in female team sport athletes, following PRISMA 2020 and PERSiST guidelines. A comprehensive search was conducted in PubMed, Scopus, and SPORTDiscus from inception to mid-January 2024. Studies were included if they examined female team sport athletes of reproductive age with regular menstrual cycles and compared the occurrence of muscle injuries across at least two menstrual phases. Studies involving hormonal contraceptive use, medications affecting the menstrual cycle or musculoskeletal system, or menstrual dysfunction were excluded. Three studies met the inclusion criteria, involving 318 participants. Meta-analysis yielded a pooled Risk Ratio of 1.18 (95% CI: 0.75 to 1.86, p = 0.46) for injury risk between the luteal and follicular phases, suggesting no statistically significant association. However, the certainty of the cumulative evidence was rated as very low due to methodological limitations, including inconsistent phase classifications and reliance on imprecise methods for identifying menstrual phases. Consequently, no practical or clinical recommendations can be made at this time. Future research employing standardised, physiologically accurate methods for classifying and detecting menstrual cycle phases is necessary to better understand the potential links between hormonal fluctuations and injury risk.
Goshtasebi A et al., 2019·Clin Endocrinol (Oxf)·Free full text on PubMed Central
Many women use combined hormonal contraceptives (CHC) during adolescence during which they are accruing peak areal bone mineral density (BMD) that relates to lifetime fracture risk. To build BMD requires formation with which CHC-related exogenous oestrogen may interfere. We compared peak BMD accrual in adolescents using and not using CHC. We performed literature searches for prospective published peer-reviewed articles providing 12to 24-month BMD change in adolescent (12to 19-year-old) women using CHC vs CHC-unexposed control women. Meta-analyses used random-effects models to assess BMD change rate at lumbar spine (LS) and other sites in adolescent CHC users vs CHC nonusers. Literature searches yielded 84 publications of which nine were eligible. Adolescent-only data were sought from cohorts with wider age inclusions. The 12-month LS meta-analysis with eight paired comparisons in 1535 adolescents showed a weighted mean BMD difference of -0.02 (95% confidence interval [CI]: -0.05 to 0.00) g/cm(2) in CHC-exposed adolescents (P = 0.04). The 24-month LS meta-analysis with five paired comparisons in 885 adolescents showed a highly significant weighted mean BMD difference of -0.02 (95% CI: -0.03 to -0.01) g/cm(2) in CHC-exposed adolescents (P = 0.0006). Heterogeneities by I(2) were 96% and 85%, respectively. Insufficient data for other bone sites precluded quantitative analysis. Given that adolescent exposure to CHC appears to be increasing, this evidence for potential impairment of peak spinal BMD accrual is of concern and suggests a potential public health problem. Randomized controlled trial data are needed to determine CHC effects on adolescent bone health.
Brajic TS et al., 2018·J Musculoskelet Neuronal Interact
To assess combined hormonal contraceptives (CHC) use and adolescent women's peak areal bone mineral density (BMD) accrual. We enrolled 527 randomly selected women across Canada (2004-6) divided by age into adolescents (16-19) and young adults (20-24) and by CHC use to ever (E-CHC)/never (N-CHC) users. At baseline and year 2 we measured height, weight, and BMD at lumbar spine (L1-4), femoral neck, and total hip sites. Interviewer-administered questionnaires addressed menarche age, cigarette and alcohol use, calcium/vitamin D intakes, physical activity and estrogen dose (≤30/>30 micrograms). Linear regression models examined associations of CHC use with 2-year BMD change adjusted for bone-related variables. Of 307 women with complete data, 229 (75%) used CHC. N-CHC adolescents gained significantly more unadjusted total hip BMD +0.012 g/cm(2)/2-y (95% C.I.: 0.001, 0.023) with similar trends at all sites. N-CHC adolescents tended to have greater adjusted femoral neck BMD gain: mean difference +0.009 g/cm(2) (95% CI: -0.002; 0.021). In young women N-CHC, however, adjusted femoral neck BMD decreased significantly more -0.021 g/cm(2) (95%CI: -0.006; -0.036) with similar trends at other sites. BMD changes were unrelated to estrogen dose and age at starting CHC. Adolescent CHC users in a random population demonstrated less hip region peak BMD accrual than non-users. This requires randomized control trial confirmation.
Questions have been raised about the effects of progestogen-only contraceptive use on bone health, particularly among young women who have not yet reached peak bone mass and perimenopausal women who may be starting to lose bone mass. We conducted a systematic review that evaluated the association between progestogen-only contraceptive use and fracture risk or bone mineral density (BMD). We identified 39 articles from MEDLINE and EMBASE, published through July 2005. One study reported that depot medroxyprogesterone acetate (DMPA) users were more likely to experience stress fractures than nonusers; this association was not statistically significant after controlling for baseline bone density. In cross-sectional studies, the mean BMD in DMPA users was usually below that of nonusers, but within 1 SD. In longitudinal studies, BMD generally decreased more over time among DMPA users than among nonusers, but women gained BMD upon discontinuation of DMPA. Limited evidence suggested that use of progestogen-only contraceptives other than DMPA did not affect BMD.
Assess the association between combined hormonal contraceptives (CHC) use and musculoskeletal tissue pathophysiology, injuries or conditions.
Systematic review with semiquantitative analyses and certainty of evidence assessment, guided by the Grading of Recommendations Assessment, Development and Evaluation approach. Data Sources: MEDLINE, EMBASE, CENTRAL, SPORTDiscus, CINAHL searched from inception to April 2022. Intervention and cohort studies that assessed the association between new or ongoing use of CHC and an outcome of musculoskeletal tissue pathophysiology, injury or condition in postpubertal premenopausal females. Across 50 included studies, we assessed the effect of CHC use on 30 unique musculoskeletal outcomes (75% bone related). Serious risk of bias was judged present in 82% of studies, with 52% adequately adjusting for confounding. Meta-analyses were not possible due to poor outcome reporting, and heterogeneity in estimate statistics and comparison conditions. Based on semiquantitative synthesis, there is low certainty evidence that CHC use was associated with elevated future fracture risk (risk ratio 1.02-1.20) and total knee arthroplasty (risk ratio 1.00-1.36). There is very low certainty evidence of unclear relationships between CHC use and a wide range of bone turnover and bone health outcomes. Evidence about the effect of CHC use on musculoskeletal tissues beyond bone, and the influence of CHC use in adolescence versus adulthood, is limited. Given a paucity of high certainty evidence that CHC use is protective against musculoskeletal pathophysiology, injury or conditions, it is premature and inappropriate to advocate, or prescribe CHC for these purposes. This review was registered on PROSPERO CRD42021224582 on 8 January 2021.
Bone Health › Hormones and Bone › Adolescent Bone Accrual · Menstrual Cycle › Cycle Disorders › Ovulatory Disturbances · Reproductive Endocrinology › Ovulation Physiology › Anovulation
Jerilynn C Prior
J Prior
PMID 28977329 28977329 DOI 10.1590/1984-0462/;2017;35;2;00019 10.1590/1984-0462/;2017;35;2;00019 Prior et al. 2017, Prior 2017
Cite this article
Prior, J. C. (2017). How can we protect peak bone mass and future bone health for adolescent women? - By supporting ovulation and avoiding combined hormonal contraception use. Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo, 35(2), 121-124. https://doi.org/10.1590/1984-0462/;2017;35;2;00019
Prior JC. How can we protect peak bone mass and future bone health for adolescent women? - By supporting ovulation and avoiding combined hormonal contraception use. Rev Paul Pediatr. 2017;35(2):121-124. doi:10.1590/1984-0462/;2017;35;2;00019
Prior, J. C. "How can we protect peak bone mass and future bone health for adolescent women? - By supporting ovulation and avoiding combined hormonal contraception use." Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo, vol. 35, no. 2, 2017, pp. 121-124.