Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-28T22:34:52.275Z Has data issue: false hasContentIssue false

Familial Occurrence of Complex Regional Pain Syndrome

Published online by Cambridge University Press:  02 December 2014

Peyman Shirani
Affiliation:
Department of Neurology, Baylor College of Medicine
Ali Jawaid
Affiliation:
Department of Neurology, Baylor College of Medicine
Paolo Moretti
Affiliation:
Department of Neurology, Baylor College of Medicine
Elham Lahijani
Affiliation:
Interventional Neurology, Inc., Houston, Texas, USA
Alicia R. Salamone
Affiliation:
Department of Neurology, Baylor College of Medicine
Paul E. Schulz
Affiliation:
Department of Neurology, Baylor College of Medicine Department of Neurology, The Methodist Hospital
Everton A. Edmondson*
Affiliation:
Department of Neurology, The Methodist Hospital Interventional Neurology, Inc., Houston, Texas, USA
*
The Methodist Hospital, 6560 Fannin St., Suite 2202, Houston, Texas, 77030, USA.
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Background:

The etiology of complex regional pain syndrome (CRPS) is unknown. Different environmental and genetic factors have been postulated to contribute to CRPS.

Methods:

We reviewed the clinical data from a cohort of 69 patients with CRPS. Four families were identified with two or more members affected with CRPS yielding a total of nine patients. Six more patients reported the presence of pain symptoms in their family members, however; this could not be clinically confirmed.

Results:

The case histories of the nine individuals with ‘familial’ CRPS suggested a younger age at onset and more frequent history of migraine versus the non-familial patients. A pattern of inheritance could not be ascertained.

Conclusion:

This data supports the hypothesis that CRPS can be familial and hence may have a genetic basis in some families. Larger studies will be needed to ascertain clearer patterns of inheritance and to determine whether the clinical features of ‘familial’ CRPS are the same as the sporadic form.

Type
Original Article
Copyright
Copyright © The Canadian Journal of Neurological 2010

References

1. Sandroni, P, Benrud-Larson, LM, McClelland, RL, Low, PA. Complex regional pain syndrome type I: incidence and prevalence in Olmsted County, a population-based study. Pain. 2003; 103(1-2):199207.CrossRefGoogle ScholarPubMed
2. de Mos, M, de Bruijn, AG, Huygen, FJ, Dieleman, JP, Stricker, BH, Sturkenboom, MC. The incidence of complex regional pain syndrome: a population-based study. Pain. 2007; 129(1-2): 1220.CrossRefGoogle ScholarPubMed
3. Allen, G, Galer, BS, Schwartz, L. Epidemiology of complex regional pain syndrome: a retrospective chart review of 134 patients. Pain. 1999; 80(3):53944.CrossRefGoogle ScholarPubMed
4. Maleki, J, LeBel, AA, Bennett, GJ, Schwartzman, RJ. Patterns of spread in complex regional pain syndrome type I (reflex sympathetic dystrophy). Pain. 2000; 88(3):25966.CrossRefGoogle ScholarPubMed
5. Harden, RN, Bruehl, S, Galer, BS, Saltz, S, Bertram, M, Backonja, M, et al. Complex regional pain syndrome: are the IASP diagnostic criteria valid and sufficiently comprehensive? Pain. 1999; 83(2):2119.CrossRefGoogle ScholarPubMed
6. Toda, K, Muneshige, H, Maruishi, M, Kimura, H, Asou, T. Headache may be a risk factor for complex regional pain syndrome. Clin Rheumatol. 2006; 25(5):72830.CrossRefGoogle ScholarPubMed
7. An, HS, Hawthorne, KB, Jackson, WT. Reflex sympathetic dystrophy and cigarette smoking. J Hand Surg. 1988; 13(3):45860.CrossRefGoogle ScholarPubMed
8. Mailis, A, Wade, J. Profile of Caucasian women with possible genetic predisposition to reflex sympathetic dystrophy: a pilot study. Clin J Pain. 1994; 10(3):2107.CrossRefGoogle ScholarPubMed
9. Kemler, MA, van de Vusse, AC, van de Berg-Loonen, EM, Barendse, GA, van Kleef, M, Weber, WE. HLA-DQ1 associated with reflex sympathetic dystrophy. Neurology. 1999; 53(6):13501.CrossRefGoogle ScholarPubMed
10. van Hilton, JJ, van de beek, WJT, Roep, BO. Multifocal or generalized tonic dystonia of complex regional pain syndrom: a distinct clinical entity associated with HLA-DR13. Ann Neurol. 2000; 48(1):1136.3.0.CO;2-9>CrossRefGoogle Scholar
11. Albert, J, Ott, H. Three brothers with algodystrophy of the hip. Ann Rheum Dis. 1983; 42(4):4214.CrossRefGoogle ScholarPubMed
12. Erdmann, MW, Wynn-Jones, CH. ‘Familial’ reflex sympathetic dystrophy syndrome and amputation. Injury. 1992; 23(2):1368.CrossRefGoogle ScholarPubMed
13. Veldman, PH, Reynen, HM, Arntz, IE, Goris, RJ. Signs and symptoms of reflex sympathetic dystrophy: prospective study of 829 patients. Lancet. 1993; 342(8878):10126.CrossRefGoogle ScholarPubMed
14. Bruscas Izu, C, Beltrán Auderá, CH, Jiménez Zorzo, F. Polytopic and recurrent reflex sympathetic dystrophy in lower limbs in two siblings. An Med Interna. 2004; 21(4):1834.Google ScholarPubMed
15. Hühne, K, Leis, S, Schmelz, M, Rautenstrauss, B, Birklein, F. A polymorphic locus in the intron 16 of the human angiotensin-converting enzyme (ACE) gene is not correlated with complex regional pain syndrome I (CRPS I). Eur J Pain. 2004; 8(3): 2215.CrossRefGoogle Scholar
16. de Rooij, AM, de Mos, M, Sturkenboom, MC, Marinus, J, van den Maagdenberg, AM, van Hilten, JJ. Familial occurrence of complex regional pain syndrome. Eur J Pain. 2009; 13(2):1717.CrossRefGoogle ScholarPubMed
17. Higashimoto, T, Baldwin, EE, Gold, JI, Boles, RG. Reflex sympathetic dystrophy: complex regional pain syndrome type I in children with mitochondrial disease and maternal inheritance. Arch Dis Child. 2008 May; 93(5):3907.CrossRefGoogle ScholarPubMed
18. Trottier, Y, Biancalana, V, Mandel, JL. Instability of CAG repeats in Huntington’s disease: relation to parental transmission and age of onset. J Med Genet. 1994 May; 31(5):37782.CrossRefGoogle ScholarPubMed
19. Rooij, AM, de Mos, M, van Hilten, JJ, Sturkenboom, MC, Gosso, MF, den Maagdenberg, AM, et al. Increased risk of complex regional pain syndrome in siblings of patients? J Pain. 2009; Dec; 10(12):12505.CrossRefGoogle ScholarPubMed
20. Grosen, D, Chevrier, C, Skytthe, A, Bille, C, Molsted, K, Sivertsen, A, et al. A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance. J Med Genet. 2009 [Epub 2009 Sep 14].Google Scholar
21. Peterlin, BL, Rosso, AL, Nair, S, Young, WB, Schwartzman, RJ. Migraine may be a risk factor for the development of complex regional pain syndrome. Cephalalgia. 2009 Jul 9 [Epub 2009 Jul 9].Google Scholar
22. Oerlemans, HM, Oostendrop, RA, de Boo, T, Goris, RJ. Pain and reduced mobility in complex regional pain syndrome I: outcome of a prospective randomized controlled clinical trial of adjuvant physical therapy versus occupational therapy. Pain. 1999; 83(1): 7783.CrossRefGoogle ScholarPubMed
23. Zollinger, PE, Tuinebreijer, WE, Kreis, RW, Breederveld, RS. Effect of vitamin C on frequency of reflex sympathetic dystrophy in wrist fractures: a randomised trial. Lancet. 1999; 354(9195): 20258.CrossRefGoogle ScholarPubMed
24. Petchkrua, W, Weiss, DJ, Patel, RR. Reassessment of the incidence of complex regional pain syndrome type 1 following stroke. Neurorehabil Neural Repair. 2000; 14(1):5963.CrossRefGoogle ScholarPubMed