Table 2.
Muscle and bone parameters | Original analyses (45 vs. 221) | Competing risk analyses a (45 vs. 249) | ||||||
---|---|---|---|---|---|---|---|---|
Unadjusted | Adjusted b | Unadjusted | Adjusted b | |||||
HR (95% CI) | P value | HR (95% CI) | P value | HR (95% CI) | P value | HR (95% CI) | P value | |
G.MaxM area (cm2) | 1.64 (1.19, 2.25) | <0.01 | 1.32 (0.91, 1.91) | 0.14 | 1.54 (1.15, 2.08) | <0.01 | 1.27 (0.89, 1.80) | 0.18 |
G.MaxM density (HU) | 1.85 (1.36, 2.51) | <0.01 | 1.49 (1.06, 2.10) | 0.02 | 1.74 (1.27, 2.37) | <0.01 | 1.43 (0.96, 2.12) | 0.08 |
G.Med/MinM density (HU) | 1.98 (1.47, 2.67) | <0.01 | 1.68 (1.20, 2.35) | <0.01 | 1.84 (1.42, 2.39) | <0.01 | 1.61 (1.16, 2.23) | <0.01 |
FN CortThick (mm) | 1.07 (0.78, 1.49) | 0.67 | 1.08 (0.76, 1.53) | 0.68 | 1.07 (0.77, 1.49) | 0.68 | 1.07 (0.74, 1.54) | 0.72 |
TH aBMD (g/cm2) | 1.80 (1.34, 2.42) | <0.01 | 1.60 (1.11, 2.31) | 0.01 | 1.72 (1.32, 2.25) | <0.01 | 1.50 (1.09, 2.08) | 0.01 |
FN aBMD (g/cm2) | 1.38 (1.01, 1.87) | 0.04 | 1.19 (0.86, 1.66) | 0.30 | 1.35 (0.94, 1.94) | 0.11 | 1.14 (0.78, 1.67) | 0.50 |
TR aBMD (g/cm2) | 1.81 (1.30, 2.52) | <0.01 | 1.48 (1.01, 2.17) | 0.04 | 1.71 (1.25, 2.34) | <0.01 | 1.40 (0.97, 2.01) | 0.07 |
IT aBMD (g/cm2) | 1.77 (1.33, 2.36) | <0.01 | 1.62 (1.13, 2.31) | 0.01 | 1.71 (1.32, 2.22) | <0.01 | 1.53 (1.13, 2.06) | 0.01 |
bCSA (cm2) | 1.59 (1.17, 2.15) | <0.01 | 1.23 (0.88, 1.72) | 0.22 | 1.54 (1.19, 1.98) | <0.01 | 1.19 (0.89, 1.58) | 0.25 |
ACT (cm) | 1.49 (1.09, 2.04) | 0.01 | 1.18 (0.83, 1.67) | 0.37 | 1.45 (1.08, 1.93) | 0.01 | 1.13 (0.80, 1.61) | 0.49 |
CSMI (cm4) | 1.35 (0.98, 1.85) | 0.06 | 1.14 (0.83, 1.56) | 0.41 | 1.35 (1.00, 1.82) | 0.05 | 1.14 (0.89, 1.46) | 0.32 |
Z (cm3) | 1.28 (0.98, 1.66) | 0.07 | 1.13 (0.83, 1.55) | 0.42 | 1.28 (0.99, 1.65) | 0.06 | 1.12 (0.86, 1.47) | 0.40 |
BR | 0.74 (0.56, 0.98) | 0.04 | 0.87 (0.64, 1.18) | 0.36 | 0.78 (0.60, 1.02) | 0.07 | 0.92 (0.66, 1.28) | 0.61 |
BMD, bone mineral density; CI, confidence interval; HR, hazard ratio; SD, standard deviance.
As for refracture risk, we did the competing risk analyses using cause‐specific hazard models given that total deaths (n = 28) occurring in the absence of refracture events are the competing risks. The Fine–Gray model was further adopted for analysing competing risks as sensitivity analyses.
Adjusted for age, sex, T2DM, and Parker Mobility Score prior to first hip fracture surgery.