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. 2015 Jul 17;97(5):506–515. doi: 10.1007/s00223-015-0037-y

Table 4.

Use of GLP-1 RAs and risk of any fracture stratified by cumulative and average daily dose

Any fracture Osteoporotic fracture
No. of cases (N = 229,145)a No. of controls (N = 229,145)a Adjusted OR (95 % CI)b No. of cases (N = 96,774)a No. of controls (N = 96,774)a Adjusted OR (95 % CI)c
Current NIAD use excl. incretins 6993 7209 Reference 3957 4058 Reference
Current GLP-1 RA use 80 71 1.16 (0.83–1.63) 23 31 0.78 (0.44–1.39)
By cumulative exposured
 0–1.4 mg 36 34 1.05 (0.63–1.73) 10 17 0.64 (0.28–1.47)
 1.4–2.7 mg 14 11 1.60 (0.69–3.69) 3 5 0.57 (0.12–2.74)
 2.7–5.5 mg 12 8 1.55 (0.60–3.95) 4 2 2.05 (0.32–13.30)
 ≥5.5 mg 18 18 0.98 (0.50–1.94) 6 7 0.93 (0.30–2.92)
By average daily dosed
 <15 mcg/day 16 19 0.91 (0.47–1.84) 3 9 0.35 (0.09–1.39)
 15–22.49 mcg/day 38 36 1.07 (0.66–1.73) 12 15 0.78 (0.35–1.75)
 ≥22.5 mcg/day 26 16 1.66 (0.86–3.19) 8 7 1.40 (0.47–4.13)
Recent GLP-1 RA use 55 56 1.03 (0.69–1.53) 23 24 0.97 (0.52–1.79)
Past GLP-1 RA use 120 93 1.09 (0.82–1.46) 47 41 0.94 (0.60–1.48)

OR odds ratio, CI confidence interval, GLP-1 RA glucagon-like peptide-1 receptor agonist, DPP4-I dipeptidyl peptidase 4 inhibitor, NIAD non-insulin anti-diabetic-drugs, COPD chronic obstructive pulmonary disease, RAAS renin–angiotensin–aldosterone system

* Statistically significant, (P < 0.05)

aThe numbers do not add up precisely to the total number of fractures because never NIAD, past NIAD and DPP4-I use are not shown

bAdjusted for history of cancer, alcoholism, COPD, fracture, rheumatoid arthritis, hyperthyroidism, secondary osteoporosis, retinopathy, neuropathy and heart failure and use of DPP4-Is, glucocorticoids, statins, antidepressants, anxiolytics, hypnotics, antipsychotics, anti-Parkinson drugs, beta-blockers, thiazide diuretics, RAAS inhibitors, loop diuretics, antiarrhythmics

cAdjusted for (a), but not for hyperthyroidism and neuropathy

dIn exenatide equivalents