This test is most useful if any of these apply to you.
Bone density helps predict fractures, but fractures also occur in people whose density doesn't meet the criteria for osteoporosis. The REMS fragility score adds an ultrasound-derived estimate of bone fragility. Higher femoral scores have predicted later hip fractures in prospective studies, though its role in choosing and monitoring treatment is less established than its ability to separate groups by risk.
This result comes from your left femoral neck. That's the narrow stretch of bone below the ball of the hip joint. REMS uses ultrasound without ionizing radiation, and portable equipment allows scanning at a bedside.
REMS stands for radiofrequency echographic multi-spectrometry. Software analyzes the returning ultrasound signals and compares their patterns with reference signals from people with and without fragility fractures. The calculation uses reference models matched to characteristics including age, sex and body size. It estimates fragility from those signal patterns.
The fragility score runs from 0 to 100, with higher values indicating greater estimated fragility. The number isn't your percentage chance of breaking a hip. The same examination also produces a separate bone mineral density estimate and T-score. A T-score compares density with a young-adult reference population.
Evidence about the femoral fragility score needs to be separated from evidence about the spine score and about REMS bone density. These are different outputs, even when they come from the same examination.
| Study | Measurement | Finding and limitation |
|---|---|---|
| 2023 prospective study: 1,679 adults completed femoral follow-up, with 48 hip fractures | Femoral fragility score | Higher scores predicted hip fractures over follow-up lasting up to five years. The score distinguished people who later fractured better than REMS or DXA T-scores, including after adjustment for age and body size. The study came from one center and included relatively few hip fractures. |
| 2026 multicenter study: 4,017 women completed follow-up | Combined REMS T-score and fragility score | Seven combined categories showed progressively higher fracture rates. Femoral categories were evaluated against hip fractures; lumbar categories were evaluated against major osteoporotic fractures. This supports combined risk assessment but doesn't establish the score's added value over a full clinical risk model. |
| 2022 study: 175 people with primary or immobility-related osteoporosis | Femoral fragility score | Scores were higher in people with a previous fracture. This was a comparison of fracture histories, not a test of future fracture prediction. |
| 2020 study: 1,370 women completed follow-up | REMS bone density T-score | A femoral T-score in the osteoporosis category was associated with about 2.8 times the odds of a later fragility fracture. This finding concerns the density result, not the fragility score. |
The direct hip-score evidence is promising. It does not yet show that adding the score to usual care prevents more fractures, or that lowering it through treatment reduces your risk. Several authors of the 2023 prediction study held stock in the device manufacturer or had an advisory relationship with it.
A 2026 study examined results from 209 people at one REMS clinic. A mathematical model using age alone accounted for more than 95% of the differences in femoral fragility scores within that group. This raises a specific question about how much information the score adds beyond age for an individual person.
The same paper also changed the age and weight entered during repeat scans of five volunteers. Those experiments changed the REMS bone density estimate despite there being no plausible corresponding change in bone over the short study period. They did not establish how much changing entered weight changes the fragility score.
The strong relationship with age and the prospective fracture findings can both be true, because age itself predicts fracture risk. The single-clinic study doesn't prove that the score contains no useful ultrasound information, but it does argue against treating the result as a direct measure of bone structure independent of age.
DXA uses low-dose X-rays to measure bone density. In a large European study, quality-checked REMS femoral density results identified about 90% of the women classified as having osteoporosis by DXA and correctly classified about 95% of those without DXA-defined osteoporosis. Those figures describe agreement between density methods, not the fragility score's accuracy for predicting fractures.
Agreement has been weaker in some other populations. Among 148 geriatric outpatients, the femoral-neck REMS density result identified only 46% of those classified as having osteoporosis by DXA. A reassuring REMS density result therefore cannot reliably exclude DXA-defined osteoporosis in a similar population.
Spinal arthritis, vertebral compression and abdominal artery calcification can inflate lumbar DXA density. Studies suggest that REMS density is less affected by some of these artifacts. That advantage concerns particular measurements and sites; it does not establish that a left-femur fragility score is more accurate whenever the two examinations disagree. Diabetes can weaken bone despite preserved density, which is a different problem from an imaging artifact.
A small study of 20 people receiving peritoneal dialysis found that changes in REMS and DXA bone density tracked poorly together. DXA detected a decline in femoral-neck density that did not reach statistical significance with REMS, but the difference between the methods' time trends was itself not statistically significant. The study did not measure treatment-related changes in fragility score.
Repeated femoral measurements can be highly reproducible under controlled conditions. Reproducibility establishes consistency; it doesn't establish that a change over months measures a treatment benefit.
A least significant change is the smallest difference expected to exceed measurement noise. A value established for REMS bone density cannot automatically be used for the fragility score. Even a score change larger than its measurement noise would need to be interpreted alongside changes in personal details, bone density and clinical risk. There is no established amount of femoral-score reduction that proves fracture risk has fallen.
Studies of osteoporosis treatment using REMS have often followed bone density. For example, a study of denosumab in women receiving breast-cancer endocrine therapy reported density changes but explicitly did not monitor fragility score. Evidence for one output cannot establish treatment response for the other.
REMS Fragility Score (Left Femur) is best interpreted alongside these tests.