Topic summary · Endocrinology

Osteoporosis

ABIM Internal Medicine high-yield one-pager — diagnosis, FRAX thresholds, risk tiers, drug-by-scenario selection, holidays, adverse effects, and board pearls.

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Updated May 2026 · Endocrinology

1Diagnosis (postmenopausal women, men ≥ 50)

T-scoreCategory
≥ −1.0Normal
−1.0 to −2.5Osteopenia (low bone mass)
≤ −2.5Osteoporosis
≤ −2.5 + fragility fxSevere (established)

Use lowest T at L1–L4 spine, femoral neck, total hip. Use 1/3 distal radius if hyperparathyroidism, body weight > table limit, or hip/spine uninterpretable.

Premenopausal women, men < 50, kids: use Z-score; ≤ −2.0 = "below expected for age" — diagnose OP only with fragility fx or secondary cause.

Clinical Dx without low T: any hip or vertebral fragility fx; OR other fragility fx + osteopenia; OR osteopenia + Fracture Risk Assessment Tool (FRAX) above threshold.

2FRAX & treatment thresholds (US)

FRAX = WHO 10-yr probability of major osteoporotic fracture (MOF; hip, clinical spine, humerus, distal forearm) and hip fx alone.

Treat if: T ≤ −2.5 · OR hip/vertebral fragility fx (any T) · OR osteopenia + FRAX MOF ≥ 20% or hip ≥ 3%.

FRAX inputs: age, sex, wt/ht, prior fx, parent hip fx, smoking, glucocorticoid (GC) use, RA, secondary OP, alcohol ≥ 3/d, ± femoral-neck bone mineral density (BMD).

FRAX caveats (under-estimates): high-dose GC (> 7.5 mg/d → ×1.15 MOF, ×1.2 hip), multiple/recent fx, type 2 diabetes mellitus (T2DM), low trabecular bone score (TBS), fall risk.

3Risk tiers (AACE 2020) — drives drug choice

TierDefiningFirst-line
HighT ≤ −2.5, or osteopenia + FRAX threshold, or older fragility fxOral bisphosphonate (BP; alendronate, risedronate); zoledronic acid (ZA) or denosumab if oral CI
Very highRecent fx (< 12 mo); fx on therapy; multiple fx; T ≤ −3.0; FRAX MOF > 30% / hip > 4.5%; high fall risk; fx on chronic GCAnabolic first (teriparatide, abaloparatide, romosozumab) → followed by antiresorptive

4Screening

  • All women ≥ 65 (USPSTF B; BHOF, AACE)
  • Postmenopausal women < 65 if elevated risk by tool
  • Men ≥ 70 (BHOF; USPSTF I-statement)
  • Anyone ≥ 50 with fragility fx
  • Chronic GC ≥ 3 mo regardless of age
  • Aromatase inhibitor (AI) use (breast ca), androgen-deprivation therapy (ADT; prostate ca)

Modality: central dual-energy X-ray absorptiometry (DXA; lumbar spine + hip). quantitative computed tomography (QCT) / peripheral DXA / US: screen only.

5Secondary-cause workup (do before treating)

Always: CBC, CMP (Ca, Cr, alk phos, albumin), 25-hydroxyvitamin D (25-OH-D), TSH, intact parathyroid hormone (PTH), 24-h urine Ca + Cr, serum protein electrophoresis (SPEP) + free light chains + urine protein electrophoresis (UPEP), tissue-transglutaminase IgA (tTG-IgA), total testosterone (men).

Selective: 24-h urine free cortisol or low-dose dex (Cushing); tryptase; iron studies; ACTH; prolactin; estradiol/FSH/LH.

Yield: ~30% women, 50–80% men have a secondary cause.

High-yield mimics: 1° hyperparathyroidism (cortical loss → low radius BMD), multiple myeloma (MM)/monoclonal gammopathy of undetermined significance (MGUS), hyperthyroidism, celiac, Cushing, hypogonadism (incl. AI/ADT), CKD–mineral bone disorder (CKD-MBD), anorexia nervosa, mastocytosis, RA, inflammatory bowel disease (IBD).

6Drug-by-scenario (memorize)

ScenarioPick
Standard postmenopausal OP, GI tolerantAlendronate or risedronate PO
Adherence concern / oral GI intoleranceZoledronic acid IV q1y
Recent hip fractureZA — mortality benefit (HORIZON-RFT)
Chronic kidney disease (CKD) estimated glomerular filtration rate (eGFR) < 35Denosumab (replete Ca/D)
AI-induced bone loss (breast ca)Denosumab q6mo or ZA
ADT bone loss (prostate ca)Denosumab 60 mg SC q6mo (HALT)
Younger postmenopausal + breast-ca riskRaloxifene (also ↓ ER+ breast ca; no hip benefit; ↑ VTE)
Newly menopausal + vasomotor sxEstrogen ± bazedoxifene
Very-high risk (recent/multiple fx, T ≤ −3.0)Anabolic first: romosozumab (no recent CV), teriparatide, or abaloparatide → then antiresorptive
Glucocorticoid-induced osteoporosis (GIO) high/very-high riskOral BP, ZA, denosumab, or PTH analog; consider anabolic first in very-high
Premenopausal OPTreat secondary cause; pharm only if fragility fx

7Drug holidays — board favorite

Risk after courseOral BPIV ZA
Low–moderateHoliday at 5 yr; reassess q2–3yHoliday at 3 yr
High / very highContinue to 10 yrContinue to 6 yr

Denosumab: NO holiday. Stopping → rebound multiple vertebral fx within 6–18 mo. Transition to BP within ≤ 6 mo of last dose.

Anabolic must be followed by antiresorptive or BMD gains lost in < 12 mo.

8Adverse effects — buzzwords

  • Osteonecrosis of the jaw (ONJ): rare at OP doses (~1/10k–100k pt-yr); ↑ with dental extraction, GC, chemo. Don't delay tx for cleanings; defer elective implants / major surgery.
  • Atypical femoral fracture (AFF): subtrochanteric / diaphyseal, transverse; prodromal thigh/groin pain; ↑ Asian, ↑ > 5 yr BP. Image bilaterally if suspected.
  • Oral BP: esophagitis — full water, upright 30–60 min, fasting; avoid if eGFR < 30–35.
  • IV ZA: acute-phase rxn (~30%) first dose; AF signal (not replicated); avoid eGFR < 35.
  • Denosumab: hypocalcemia (esp CKD); cellulitis; rebound vertebral fx on stop.
  • Romosozumab: Boxed warning (BBW) ↑ MI, stroke, CV death (ARCH); contraindicated within 1 yr of MI/stroke.
  • Teriparatide: prior osteosarcoma BBW removed 2020; still avoid prior radiation, Paget, ↑ alk phos.
  • Raloxifene: ↑ venous thromboembolism (VTE); worsens hot flashes.

9Special populations

GIO (ACR 2022): any adult on prednisone ≥ 2.5 mg/d for > 3 mo → assess. Treat moderate / high / very-high risk pharmacologically. Anabolic agents conditionally recommended initial therapy in high or very-high risk. Continue therapy as long as GC continues.

Men: approved — alendronate, risedronate, ZA, denosumab, teriparatide, abaloparatide, romosozumab. Always check testosterone.

CKD: eGFR ≥ 35 → standard. eGFR 30–35 → avoid IV ZA. eGFR < 30 → exclude CKD-MBD; denosumab (watch hypoCa); teriparatide / abaloparatide if PTH not high.

Cancer-induced: AI in breast ca → denosumab or ZA. ADT prostate → denosumab q6mo (HALT: −62% vert fx).

Older adults: falls dominate; multifactorial fall prevention; parenteral therapy preferred when adherence poor.

10Calcium / vit D / lifestyle

  • Calcium 1200 mg/d women ≥ 51 + men ≥ 71; 1000 mg/d men 50–70. Diet preferred (excess → kidney stones).
  • Vitamin D 800–1000 IU/d; target 25-OH-D ≥ 30 ng/mL (AACE), ≥ 20 ng/mL (IOM).
  • Weight-bearing + resistance + balance exercise.
  • Smoking cessation; alcohol < 2/d (♀) / 3/d (♂); protein ≥ 1 g/kg/d.
  • Fall prevention: review meds, vision, home, footwear.

11Monitoring

  • DXA at 1–2 yr after start, then q2–3y if stable; same machine; change must exceed least significant change (LSC).
  • C-terminal telopeptide (CTX) (resorption) / procollagen type 1 N-terminal propeptide (P1NP) (formation) at 3–6 mo for adherence/response; expect 30–50% suppression on antiresorptive, rise on anabolic.
  • Treatment failure = ≥ 2 fragility fx on therapy or BMD ↓ > LSC despite adherence → re-eval secondary causes; switch (often to anabolic).

12Top board pearls

  • ~⅔ of vertebral fx are clinically silent → vertebral fracture assessment (VFA) on DXA if height loss or chronic GC.
  • Hip fx: 25–30% 1-yr mortality; about half never regain their prior level of function.
  • 1° hyperparathyroidism preferentially affects cortical bone → check 1/3 distal radius.
  • T2DM: BMD overestimates strength → use TBS / FRAX adjustment.
  • Recent hip fx: give ZA — both fracture and mortality benefit (HORIZON-RFT, > 2 wks post-op).
  • Don't stop denosumab cold — rebound vertebral fx within months.
  • Anabolic first in very-high risk; reverse sequence (anabolic after BP/denosumab) blunts response.
  • Romosozumab BBW = CV; alternative anabolic if recent MI/stroke.
  • Premenopausal "OP" is almost always secondary — work up first.
  • Asian ancestry + long-duration BP → AFF risk.
  • Calcitonin and ibandronate: no hip-fx data — wrong answer for hip protection.
  • Teriparatide / abaloparatide: up to 24 months — continue beyond only if high fracture risk persists.

13 · Abbreviations

25-OH-D
25-hydroxyvitamin D
AACE
Am. Assoc. Clinical Endocrinologists
ACR
Am. College of Rheumatology
ACTH
adrenocorticotropic hormone
ADT
androgen-deprivation therapy
AF
atrial fibrillation
AFF
atypical femoral fracture
AI
aromatase inhibitor
alk phos
alkaline phosphatase
ASBMR
Am. Soc. Bone & Mineral Research
BBW
boxed (black-box) warning
BHOF
Bone Health & Osteoporosis Foundation
BMD
bone mineral density
BP
bisphosphonate
Ca
calcium
CBC
complete blood count
CI
contraindication / contraindicated
CKD
chronic kidney disease
CKD-MBD
CKD–mineral bone disorder
CMP
comprehensive metabolic panel
Cr
creatinine
CTX
C-terminal telopeptide
CV
cardiovascular
DXA
dual-energy X-ray absorptiometry
eGFR
estimated glomerular filtration rate
ER+
estrogen-receptor positive
FDA
U.S. Food and Drug Administration
FRAX
Fracture Risk Assessment Tool (WHO)
FSH
follicle-stimulating hormone
fx
fracture
GC
glucocorticoid
GI
gastrointestinal
GIO
glucocorticoid-induced osteoporosis
HRT
hormone replacement therapy
IBD
inflammatory bowel disease
IOM
Institute of Medicine
IU
international units
IV
intravenous
LH
luteinizing hormone
L1–L4
lumbar vertebrae 1–4
LSC
least significant change
MGUS
monoclonal gammopathy of undetermined significance
MI
myocardial infarction
MM
multiple myeloma
MOF
major osteoporotic fracture
NOF
National Osteoporosis Foundation (now BHOF)
ONJ
osteonecrosis of the jaw
OP
osteoporosis
P1NP
procollagen type 1 N-terminal propeptide
PO
oral (per os)
PTH
parathyroid hormone
QCT
quantitative computed tomography
RA
rheumatoid arthritis
SC
subcutaneous
SPEP
serum protein electrophoresis
T2DM
type 2 diabetes mellitus
TBS
trabecular bone score
tTG-IgA
tissue-transglutaminase IgA
TSH
thyroid-stimulating hormone
UPEP
urine protein electrophoresis
US
ultrasound
USPSTF
U.S. Preventive Services Task Force
VFA
vertebral fracture assessment
VTE
venous thromboembolism
WHO
World Health Organization
ZA
zoledronic acid
Anchored to USPSTF 2025 · BHOF 2022 · AACE 2020 · Endocrine Society 2019/2020 · ACR 2022 (GIO) · ASBMR consensus statements. Trial names cited in §6/§8 (HORIZON-RFT, ARCH, FRAME, FREEDOM, FIT, MORE, HIP, BONE, DIVA, ACTIVE, HALT, PROOF) are fully cited in the companion clinical reference. Educational use only — verify dosing and contraindications against current FDA labeling and your local practice before acting.