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Rheumatoid arthritis, bone and drugs: a dangerous interweave
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  1. Salvatore Minisola,
  2. Jessica Pepe,
  3. Cristiana Cipriani
  1. Department of Clinical, Internal, Anaesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Roma, Italy
  1. Correspondence to Dr Salvatore Minisola, Department of Clinical, Internal, Anaesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Roma 00185, Italy; salvatore.minisola{at}uniroma1.it

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Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory condition that leads, per se, to bone loss by three main mechanisms. The first one is represented by bone erosions around the involved joints. Second, there is focal subchondral bone loss owing to increased osteoclast activity. Finally, systemic inflammation causes universal bone loss, mainly manifesting at the axial skeleton (ie, vertebral bodies and hip).1 On the top of this, physical inactivity, also related to lower muscle mass and sarcopenia, further exacerbates bone loss. As a consequence, osteoporosis can be detected in 30%–50% of patients with RA, also depending on age and sex; prevalence and fracture risk both raise with disease duration and seropositivity.2 The importance of RA in determining both local and systemic osteoporosis is emphasised by the fact that RAis an input variable, as independent risk factor, in the calculation of future fracture risk by FRAX.

It is also well known that patients with RA consume a number of drugs to mainly counteract inflammation and pain. However, some of the drugs used have detrimental effects on skeletal tissue, reducing bone strength and ultimately leading to fractures.

About 1% of adults in Britain and USA receive long-term oral glucocorticoids mainly for the treatment of joint problems but also for digestive and cutaneous diseases.3 4 The long-term or high doses of glucocorticoids use is associated with reduced skeletal strength; indeed, glucocorticoid induced osteoporosis is the most prevalent cause of secondary osteoporosis. Glucocorticoids exert their deleterious effects on bone by acting on the three main cell skeletal lines (osteoblasts, osteoclasts end osteocytes). Among the most important negative effects are: (1) a preferential differentiation of pluripotent precursor cells to adipocytes rather than osteoblasts; (2) a stimulation of the receptor activator of nuclear factor-kB (RANK)-RANK ligand (RANKL) production which at least initially increase bone resorption and (3) an increased apoptosis of osteocytes with changes in the physical and fluid characteristics of the surrounding territory. These negative effects at the cellular levels contribute to increase the risk of fracture, together with the effects on other organs such as muscle (steroid myopathy) and eye (increased intra-articular pressure and formation of posterior subcapsular cataracts).5

Proton pump inhibitors (PPI) are drugs widely prescribed in the world. When Food and Drug Administration approved its use as an ‘over-the-counter’ drug, there has been a skyrocketing increase in their consumption. Data in Europe mirrored this trend.6 However, PPIs are associated with a number of side effects among which an increased risk of fracture. Indeed, a number of meta-analyses showed a significantly increased risk of hip and vertebral fractures, with some of them also suggesting a dose–dependent relationship.7 8 However, while the biological mechanisms leading to fractures in patients taking glucocorticoids are well ascertained, the same is not true for PPI. Hypothetical mechanisms include a reduced intestinal calcium absorption related to the hypochloridria induced by the negative effects on H+/K+ ATPase activity. The absorption of other micronutrients important for skeletal health are also adversely affected by long-term PPI use; in particular, PPIs use may be associated with hypomagnesaemia and a dose-response between the PPIs use and development of hypomagnesaemia has been reported.9 Other putative mechanisms include an excessive histamine production driven by hypergastrinaemia activated enterochromaffin-like cells (possibly leading to enhanced osteoclastogenesis and bone resorption) together with vitamin B12 deficiency. The last one has been associated with an increased risk of falls and with an increased risk of fractures.10 11

In this context, Abtahi et al12 add important information with implications in clinical practice that should change our behaviour. In summary, they showed that patients with RA taking both GC and PPI have a 1.6-fold increased risk of osteoporotic fractures (hip, clinical vertebral, pelvis and ribs) compared with non-users but also with single users or oral GC or PPI.12 Merits of this investigation include the large database used together with a long observation period (ie, more than 9 years). However, there are also important weaknesses in addition to those listed by the authors. The most important is represented by the lack of full control for bone active drugs taken by the patients, also including calcium and vitamin D. They claim that these drugs ‘were not considered in the main analysis because of the accompaniment of their prescription with those of oral glucocorticoids and we expect them to lie in the causal pathway of the intended associations of mediators’. However, they do not show any evidence of this assumption nor the use of these drugs in the past 6 months is a guarantee for continuous use during the whole observation period. In addition, and most importantly, their data are not from a randomised controlled study; therefore, confounding cannot be excluded. For example, the populations considered might differ in terms of other factors that predispose or prevent fractures, such as the frequency and type of contact with care health system, physician prescribing attitudes and so on.

Bearing in mind these limitations, the most important message coming from this paper is a call for a watchful behaviour by doctors taking care of patients with RA on concurrent GC and PPI treatment. Interestingly, this dangerous liaison has been highlighted in an almost contemporary paper by Miyano et al13 in patients with anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis.

Abtahi and coworkers conclude that fracture risk assessment could be considered when a patient with RA is coprescribed oral glucocorticoids and PPIs. This approach that we would say ‘must’ be considered, does not preclude an integration with another approach represented by reducing or de-prescribing drugs when they are not needed or when their use is not fully supported by the evidence. This is particularly true, considering the significant number of drugs prescribed to patients with RA that have been associated with an increased risk of fractures.14

As far as glucocorticoids, the first step should be an attempt to minimise the use of oral glucocorticoids in terms of both dosage and duration. Then, there is clear evidence that the combination of glucocorticoids with non-steroidal anti-inflammatory drugs increase the risk of peptic ulcer disease, thus justifying the concomitant use of PPI. However, there is conflicting evidence about the risk of peptic ulcer disease in patients taking glucocorticoid monotherapy. In a nested case–control study of Medicaid patients, there was no increased risk of peptic ulcer disease at any dose or length of glucocorticoid treatment.15 Looking for example at figure 1 (considering the pharmacological history in the 6 months before), only in 2954 patients the use of PPIs seems justified in those already taking steroids (2309 patients taking NSAIDs, 409 Cox-2 selective inhibitors, 198 with gastro-oesophageal reflux and 38 with peptic ulcer disease) leaving the remaining 30.5% coprescriptions not appropriate or at least debatable. On the other hand, inappropriateness is also present in those taking steroids alone (1202, 205, 94 and 15 patients respectively) and in majority of those taking PPIs alone. This last group, points once again on the long-standing debate on overcoming resistance on deprescribing PPI.16

In those taking PPIs, an alternative approach to circumvent low calcium absorption due to hypochloridria (with subsequent skeletal loss owing to secondary hyperparathyroidism) may be represented by the administration of calcium citrate. This is because calcium carbonate is not soluble in water thus needing adequate acid secretion for ideal absorption. It has also the advantage of an optimal absorption independent of food intake.17 Furthermore, alternative therapies (at least in the first instance) including antacids, alginates or histamine type-2 receptor antagonists can be attempted.

In conclusion, the paper by Abtahi et al,12 brings to the light an important issue focusing on multiple coprescription of drugs potentially detrimental for skeletal health in patients ith RA. This aspect is often disregarded in clinical practice not only by general practitioners but also in referral centres. Add another drug to protect bone is an option; a number of studies in general not specifically targeted to patients with RA,18 have shown satisfactory results in terms of bone mineral density increase and fracture risk reduction in patients taking oral glucocorticoids.19–22 However, also reconsidering drug prescription is a suitable alternative to follow. Our suggested approach to protect bone in patients with RA taking steroids in addition to multidrug therapy is summarised in box 1.

Box 1

Skeletal protection in patients with rheumatoid arthritis on steroids and multidrug therapy

  1. Reduce glucocorticoids dose and consider glucocorticoids sparing treatments.

  2. Improve nutrition (protein, calcium and vitamin D).

  3. Adopt a healthy lifestyle (avoid tobacco, alcohol and perform physical activities and weight-bearing exercises).

  4. Evaluate the panel of drugs prescribed.

  5. Deprescribe, if possible, or consider alternatives drugs not harmful to bone.

  6. Consider prescription of bone active drugs.

  7. Monitor and reassess when indicated.

References

Footnotes

  • Handling editor Josef S Smolen

  • Contributors Intellectual concept of the editorial and approval of the submitted version.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Patient consent for publication Not required.

  • Provenance and peer review Commissioned; internally peer reviewed.

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