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93 pcnt of these Lupus patients supplemented with Vitamin D - Nov 2020

Fracture risk in systemic lupus erythematosus patients over 28 years

Rheumatology (Oxford). 2020 Nov 22;keaa705. doi: 10.1093/rheumatology/keaa705
Daniela Garelick 1, Sara Moreira Pinto 2, Filipa Farinha 3, Tatiana Pires 4, Emon Khan 3, David Isenberg 3

VitaminDWiki

Note: No statistically increased fracture risk with Lupus is not a surprise since 93% were taking Vitamin D

Falls and Fractures category contains the following

Falls

Fracture

Increased use of D has the following

People have been noticing, and increasing vitamin D (55 items)

Studies are showing increased Vitamin D consumption and associated
      Increased levels of vitamin D PLUS increased health

More people with more than 50 ng is.gd/50ngVitD


Objectives: Chronic glucocorticoid use is complicated by osteoporosis and increases the risk of fragility fractures. EULAR guidelines on SLE management recommend reducing chronic glucocorticoid dosage to ≤7.5 mg/day to minimize this risk. We examined the relationship of glucocorticoid dose to fragility fracture risk in a cohort of SLE patients.

Methods: Retrospective analysis of SLE patients attending University College Hospital over 28 years was undertaken. Collected data included consecutive steroid dose, dual-energy X-ray absorptiometry scans and fragility fractures.

Results: We collected data on 250 patients with a median of 17 years' follow-up. Fragility fractures were diagnosed in 28 (11.2%) patients and the mean ± s.d. age of first fracture was 51 ± 16 years. A total of 94% received glucocorticoids, the average dose being 6.20 mg/day. Patients with fragility fractures had a lower average daily dose (5.36 vs 6.23 mg/day) but a higher median cumulative dose (25.19 vs 20.96 g). These differences were not significant (P = 0.127 and 0.229, respectively). Some 93% of patients received vitamin D, and 85% received calcium. Cox regression analysis showed older age at SLE diagnosis, osteoporosis and secondary hyperparathyroidism were associated with fragility fractures. Glucocorticoid dose was not significantly associated with the occurrence of fragility fractures. Twenty-two patients with fractures were treated with bisphosphonates, two with denosumab and two with teriparatide.

Conclusions: We found no significant association between glucocorticoid treatment and fragility fractures in our group of patients; however, a prospective study including more patients not treated with CS would be necessary to confirm these results.


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