Table 4

Factors with a confirmed or potential anti-OP effect and bone turnover markers*†

AllRACTDVasculitidesSpondyloarthritides
N=1066N=434N=281N=173N=178
Treatment of underlying disease
 csDMARDs‡637 (60)288 (66)210 (75)81 (47)58 (33)
 Biologics313 (29)154 (36)38 (14)24 (14)97 (55)
  TNF-alpha antagonists§ (n, % of total biologics)134 (43)76 (49)1 (3)057 (59)
  IL-6R antagonists¶47 (15)33 (21)4 (11)10 (42)0
  Rituximab57 (18)25 (16)18 (47)14 (58)0
  Abatacept23 (7)20 (13)1 (3)02 (2)
  IL-17 and IL-12/23 antagonists**38 (12)00038 (39)
  Belimumab15 (5)015 (40)00
 tsDMARDs††26 (2)18 (4)1 (<1)07 (4)
Antiosteoporotic therapy
 Vitamin D supplementation865 (81)365 (84)250 (89)144 (83)87 (49)
 Calcium supplementation51 (5)24 (6)18 (6)6 (4)3 (2)
 Bisphosphonates‡‡124 (12)60 (14)31 (11)29 (17)4 (2)
 Denosumab32 (3)13 (3)10 (4)6 (4)3 (2)
 Teriparatide2 (<1)2 (1)000
 Strontium ranelate1 (<1)01 (<1)00
Behavioural
 Sun exposure (>30 min/day)490 (47)218 (51)111 (40)82 (49)79 (44)
 Non-smoker (never)540 (51)214 (50)171 (61)85 (50)70 (39)
  Former smoker347 (33)138 (32)71 (25)72 (42)66 (37)
  Active smoker§§171 (16)78 (18)38 (14)13 (7)42 (24)
 No Alcohol consumption487 (46)216 (51)141 (50)72 (43)58 (33)
 Regular physical exercise658 (63)257 (61)173 (63)113 (67)115 (67)
Laboratory tests
 S-25-hydroxy vitamin D (nmol/L) (50–150), median (IQR)80.0 (61–97)78.2 (62–96)85.8 (67.7–103)86.4 (71.0–97.6)67.7 (49.8–6.8)
 Vitamin D deficiency¶¶123 (14)50 (11)29 (13)11 (8)43 (25)
 S-osteocalcin (ng/mL) (11.0–46.0)12.3 (8–18)12.6 (9–17)11.8 (8–17)9.9 (7–16)14.6 (11–21)
 S-BAP (µg/L) (5.5–38.0)16.9 (13–21)17.2 (14–22)15.3 (12–20)15.0 (11–19)19.3 (16–25)
 S-AP (U/L) (35–130)66 (66–81)67 (56–82)61 (50–75)64 (54–84)70 (60–86)
 Gamma-GT (U/L) (5–61)24 (17–39)23 (16–36)23 (15–35)29 (19–48)24 (17–44)
 Urinary deoxypyridinoline (nmol/L) (<64)43 (23–76)48 (25–81)35 (17–76)39 (18–59)47 (27–82)
  • * Continuous variables are presented as mean values with SD unless otherwise noted.

  • † Categorical variables are presented as number and per cent of valid observations (%) unless otherwise noted.

  • ‡csDMARDs include azathioprine, chloroquine, ciclosporin, cyclophosphamide, hydroxychloroquine, leflunomide, methotrexate, mycophenolate mofetil and sulfasalazine.

  • §TNF-alpha antagonists include adalimumab, certolizumab, etanercept, infliximab and golimumab, both originator products as well as biosimilars.

  • ¶IL-6R antagonists include tocilizumab and sarilumab.

  • **IL-17 and IL-12/23 antagonists include secukinumab, ixekizumab, guselkumab, brodalumab and ustekinumab.

  • ††tsDMARDs include tofacitinib, baricitinib and apremilast.

  • ‡‡Bisphosphonates include alendronate, ibandronate, risedronate, pamidronic acid and zoledronate.

  • §§Active smoking is a known risk factor for OP and is only listed in this table for completeness of information.

  • ¶¶Vitamin D deficiency is defined as serum 25-hydroxy vitamin D level below the lower range of normal <50 nmol/L.

  • csDMARD, conventional synthetic disease-modifying antirheumatic drug; CTD, connective tissue disease; Gamma-GT, gamma-glutamyltransferase; IL, interleukin; OP, osteoporosis; RA, rheumatoid arthritis; S-AP, serum alkaline phosphatase; S-BAP, serum bone alkaline phosphatase; S-CRP, serum C reactive protein; TNF, tumour necrosis factor; tsDMARD, targeted synthetic disease-modifying antirheumatic drug.