Why do some young adults develop osteoporosis?

By Sina Hartung, MMSC-BMI, Harvard Medical SchoolReviewed by Eureka Health Medical Group
Published: July 9, 2025Updated: July 9, 2025

Key Takeaways

Most cases of osteoporosis in people under 40 result from an underlying medical problem or lifestyle factor that disrupts bone formation, such as eating disorders, long-term steroid use, endocrine disorders like hyperthyroidism, celiac disease, heavy alcohol intake, or extremely low vitamin D. Identifying and treating the root driver early can often halt bone loss and even improve bone density within 12–24 months.

Why would a 20-something develop brittle bones?

Peak bone mass is normally reached by age 30, so significant loss before then signals an imbalance between bone building and breakdown. "In young adults we almost always find a clear trigger—whether hormonal, nutritional, or drug-related," explains the team at Eureka Health. Quick identification is key because bone can still recover if the driver is removed.

  • Family history increases baseline riskHaving a parent with osteoporosis doubles a young adult’s likelihood of low bone density, even before other factors are added.
  • Hormone disorders blunt bone formationConditions such as hyperthyroidism, uncontrolled type 1 diabetes, or loss of menstrual periods lower osteoblast activity and speed up bone resorption.
  • Glucocorticoid medications weaken bone within monthsDaily prednisone ≥7.5 mg for 3 months can drop lumbar spine density by 4 %—enough to place a small-framed woman in the osteoporotic range.
  • Eating disorders rob the skeleton of raw materialsIn anorexia nervosa, up to 50 % of women have a T-score below –2.5 because protein, calcium, and estrogen are all deficient.
  • Malabsorption hinders calcium and vitamin D uptakeCeliac disease often precedes osteoporosis by years; 35 % of newly diagnosed patients already have fragility-level bone density.
  • Inherited collagen or WNT-pathway gene variants can trigger osteoporosis in otherwise healthy young adultsLoss-of-function mutations in type I collagen, LRP5, WNT1, PLS3 or SGMS2 disrupt bone matrix architecture and have been documented as primary causes of early-onset fragility, underscoring the need for genetic testing when routine labs are normal. (PMC)
  • Screening studies find 2 % of college women already meet osteoporosis criteriaA campus bone-density survey cited that 1 in 50 women had T-scores below –2.5 and another 15 % were osteopenic, indicating that low bone mass is not confined to older populations. (EverydayHealth)

Which symptoms and test results should make a young adult worry about osteoporosis?

Osteoporosis is often silent until a bone breaks, but there are subtle clues. "Unexplained height loss or stress fractures in the foot are red flags we never ignore," notes Sina Hartung, MMSC-BMI.

  • Back pain after minor strain deserves imagingCompression fractures of the thoracic spine can occur after lifting a suitcase—an unusual event in healthy young bone.
  • Recurrent stress fractures signal bone fragilityTwo or more metatarsal or tibial stress fractures in one year warrant a DXA scan, even in athletic teenagers.
  • Height loss of ≥2 cm since adolescence is suspiciousVertebral wedging can go unnoticed; measuring actual standing height is a low-tech but powerful screening tool.
  • DXA T-score below –2.5 confirms diagnosisWhen a T-score reaches osteoporotic range in a person under 40, secondary causes are present 80 % of the time.
  • Low-trauma fractures are diagnosticBreaking the wrist from a fall at standing height meets criteria for osteoporosis regardless of DXA results.
  • Z-score ≤ –2 on DXA is below expected range for ageInternational Society for Clinical Densitometry guidance cited by Herath et al. notes that a DXA Z-score of –2.0 or lower in premenopausal women or men under 50 should trigger a search for secondary osteoporosis. (Wiley)
  • Half of pre-50 osteoporosis cases stem from secondary causesA review reported that nearly 50 % of young adults with osteoporosis have an underlying disease or medication exposure—glucocorticoids being the most frequent association. (ReumatolClin)

Are certain medical conditions in youth silent drivers of bone loss?

Yes. “Thyroid, parathyroid, and gut disorders frequently hide behind early bone loss,” says the team at Eureka Health. A clinician should screen for these conditions once osteoporosis is detected.

  • Thyrotoxicosis accelerates bone turnoverHigh free-T4 shortens the bone remodeling cycle from 200 to 100 days, leaving less time for full mineralization.
  • Type 1 diabetes impairs collagen cross-linkingPoor glycemic control (HbA1c >8.5 %) reduces bone strength independent of BMD, raising fracture risk 3-fold.
  • Untreated celiac disease causes chronic calcium lossMarsh 3 villous atrophy cuts calcium absorption by up to 70 %, explaining the high prevalence of osteoporosis at diagnosis.
  • Hypogonadism removes anabolic sex hormonesLow estradiol (<20 pg/mL) or testosterone (<200 ng/dL) drops bone density 1–2 % per year until corrected.
  • Chronic kidney disease disturbs vitamin D activationeGFR <60 mL/min causes low 1,25-dihydroxyvitamin D, secondary hyperparathyroidism, and cortical bone thinning.
  • Secondary factors account for most early osteoporosisScreening is essential because up to 90 % of adolescents and young adults presenting with osteoporosis harbor an underlying disease or medication exposure rather than primary bone fragility. (Springer)
  • Hyperparathyroidism selectively thins cortical boneChronic excess parathyroid hormone accelerates osteoclastic resorption at cortical sites such as the distal radius, making early parathyroid assessment critical when unexplained bone loss is found. (MDPI)

What can a young person do right now to protect and rebuild bone?

Lifestyle changes make a measurable difference within months. "Because their bones are still remodeling rapidly, young adults can gain back density faster than older patients," emphasizes Sina Hartung, MMSC-BMI.

  • Increase dietary calcium to 1,200 mg dailyThree servings of dairy or fortified alternatives plus leafy greens provide the target intake recommended by the Endocrine Society.
  • Aim for serum 25-OH-vitamin D above 30 ng/mLDaily sunlight plus 600–1,000 IU vitamin D3 supplementation helps reach this level in most climates.
  • Add high-impact, weight-bearing exerciseJump training three times per week improved hip BMD by 2 % in female military recruits within six months.
  • Limit alcohol to ≤2 standard drinks per dayHeavy intake (≥3 drinks) doubles fracture risk; reducing use quickly lowers bone turnover markers.
  • Stop smoking completelyNicotine directly suppresses osteoblasts; cessation is linked to a 1 % BMD gain in the first year.
  • Build peak bone mass before age 30 to cut future fracture riskThe National Spine Health Foundation notes that peak bone mass is usually reached in the late twenties, and falling short of this benchmark increases osteoporosis and fracture risk later in life—highlighting the value of early nutrition and exercise. (NSHF)
  • Request a DXA scan if you have secondary causes or an unexplained fractureVanderbilt Health recommends that young adults with risk factors such as long-term steroid use, eating disorders, or a low-impact fracture obtain a dual-energy X-ray absorptiometry scan to objectively measure bone density and guide therapy. (VUH)

Which blood tests, imaging studies, and medications are used when osteoporosis strikes early?

Diagnostic work-up must be broad. "A basic ‘bone panel’ alone is not enough; we routinely add endocrine and malabsorption labs," reports the team at Eureka Health.

  • Comprehensive labs uncover secondary causesCBC, CMP, PTH, TSH, free-T4, celiac antibodies, 25-OH-vitamin D, testosterone/estradiol, and fasting cortisol form the core panel.
  • DXA plus vertebral fracture assessment (VFA)VFA detects asymptomatic spine fractures, present in 20 % of young adults with low BMD.
  • High-resolution CT clarifies microarchitectureIn selected cases, HR-pQCT reveals trabecular defects even when DXA T-scores look borderline.
  • Bone turnover markers guide therapy responseSerum P1NP drop of ≥30 % at 3 months suggests antiresorptive therapy is effective.
  • Medications are personalized and monitoredEndocrinologists may choose bisphosphonates, anabolic agents, or off-label teriparatide for severe cases, but only after reversible causes are managed.
  • Secondary causes dominate early-onset casesUp to 90 % of children and young adults with low bone density have an identifiable disease or medication driving bone loss, making the broad laboratory screen indispensable. (Springer)
  • Drug safety evidence is sparse in premenopausal patientsBisphosphonates, teriparatide, and denosumab can increase BMD, but long-term safety during potential pregnancies is unclear and no studies confirm short-term fracture prevention in this group. (T&F)

Frequently Asked Questions

This content is for informational purposes only and is not intended as medical advice. Always consult with a qualified healthcare provider for diagnosis, treatment, and personalized medical recommendations.

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