Skip to main content
Log in

Can clodronate be effective in the treatment of disabling hydroxyapatite crystal-deposition disease? A report of two cases

  • Short Communication
  • Published:
Rheumatology International Aims and scope Submit manuscript

Abstract

Hydroxyapatite crystals are often deposited in the vicinity of joints, where they can cause a clinical periarthritis. Clodronate is a first-generation bisphosphonate that has the ability to reduce ectopic calcifications. Two women were affected by disabling calcific periarthritis of the shoulders lasting for years and resistant to any traditional drug (including glucocorticoids), infiltration and surgical treatment. We treated both patients with low-dose methylprednisolone added to intramuscular clodronate at the daily dose of 100 mg administered for 20 days every 3 months for 5 cycles (18 months). In both cases, the results were clinically evident within 1 month, showing a significant reduction in pain and disability. After 18 months, the result was furthermore radiologically evident in both cases with a great reduction in the size of calcifications. These improvements were still present at follow-up after 7 and 5 years with complete functional recovery.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Abbreviations

HA:

Hydroxyapatite

CLO:

Clodronate

BP:

Bisphosphonate

HADD:

Hydroxyapatite crystal-deposition disease

GC:

Glucocorticoids

MP:

6-Methylprednisolone

im:

Intramuscular

iv:

Intravenous

References

  1. Dieppe PA, Crocker P, Huskisson EC, Willoughby DA (1976) Apatite deposition disease. A new arthropathy. Lancet 1:266–269

    Article  CAS  PubMed  Google Scholar 

  2. Bonavita JA, Dalinka MK, Schumacher HR Jr (1980) Hydroxyapatite deposition disease. Radiology 134:621–625

    CAS  PubMed  Google Scholar 

  3. McCarty GM (1998) Crystal related arthropathies. In: Klippel JH, Dieppe PA (eds) Rheumatology, 2nd edn. Mosby, London (section 8)

    Google Scholar 

  4. Garcia GM, McCord GC, Kumar R (2003) Hydroxyapatite crystal deposition disease. Seminar Musculoskelet Radiol 7:187–193

    Article  Google Scholar 

  5. Pfister J, Gerber H (1997) Chronic calcifying tendinitis of the shoulder-therapy by percutaneous needle aspiration and lavage: a prospective open study of 62 shoulders. Clin Rheumatol 16:269–274

    Article  CAS  PubMed  Google Scholar 

  6. Fleisch H (1998) Bisphosphonates: mechanism of action. Endocr Rev 19:80–100

    Article  CAS  PubMed  Google Scholar 

  7. Nancollas GH, Tang R, Phipps RJ, Henneman Z, Gulde S, Wu W et al (2006) Novel insight into actions of bisphosphonates on bone: differences in interactions with hydroxyapatite. Bone 38:617–627

    Article  CAS  PubMed  Google Scholar 

  8. Bevilacqua M, Dominguez LJ, Rosini S, Barbagallo M (2005) Bisphosphonates and atherosclerosis: why? Lupus 14:1–7

    Article  Google Scholar 

  9. Ylitalo R, Syvala H, Touhimaa P, Ylitalo P (2002) Suppression of immunoreactive macrophages in atheromatous lesions of rabbits by clodronate. Pharmacol Toxicol 90:139–143

    Article  CAS  PubMed  Google Scholar 

  10. Fujii N, Hamano T, Isaka Y, Ito T, Imai E (2005) Risedronate: a possible treatment for extraosseous calcification. Clin Calcium 15:S1 75–S1 78

    Google Scholar 

Download references

Conflict of interest

None.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gianantonio Saviola.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Saviola, G., Abdi-Ali, L., Baiardi, P. et al. Can clodronate be effective in the treatment of disabling hydroxyapatite crystal-deposition disease? A report of two cases. Rheumatol Int 31, 415–417 (2011). https://doi.org/10.1007/s00296-010-1575-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00296-010-1575-2

Keywords

Navigation