Assessment of disability in patients with alkaptonuria
Alexander V. Kuzin , Elena M. Zaytseva , Vera N. Amirdzhanova , Sergey A. Makarov , Jahangir S. Agzamov , Khalid G. Ismailov , Vadim V. Zar , Elena A. Dolzhenkova , Natalia N. Politova
Medical and Social Expert Evaluation and Rehabilitation ›› 2020, Vol. 23 ›› Issue (2) : 42 -45.
Assessment of disability in patients with alkaptonuria
Background. Alkaptonuria is an orphan, autosomal recessive disease in which clinical symptoms debut in adulthood and are characterized by progressive degenerative changes in large joints (knee, hip, shoulder) and the spine, often leading to the need for joint replacement. Developing changes often lead to persistent disability.
The purpose of this study was to evaluate disability among adult patients with alkaptonuria.
Materials and methods. The study included 46 adult patients (31 m − 67.4% and 15 w − 32.6%) with a reliable diagnosis of alkaptonuria at the age of 20 to 76 years (avg age 56.83 ± 10.52). The assessment of the presence of a disability group at the time of patients’ treatment to a rheumatologist was carried out.
Results. It turned out that disability was determined in 34 (75.6%) patients, there were no signs of persistent disability in 11 patients (24.4%). Among the patients who had signs of persistent disability, most often during the survey period, group 2 disability was established (61.8%), the differences between this and other groups were statistically significant (p < 0.05). For the first time, disability in the study cohort of patients was established at the age of 31 to 59 years (the average age was 50.83 ± 5.5 years).
Conclusions. It is important to note that in the vast majority of cases, persistent disability occurs in patients who were of working age, which underscores the importance of alkaptonuria as a medical and social problem.
alkaptonuria / ochronosis / arthropathy / disability
| [1] |
Vilboux T, Kayser M, Introne W, Suwannarat P, et al. Mutation spectrum of homogentisic acid oxidase (HGD) in alkaptonuria. Hum Mutat. 2009;30(12):1611-1619. https://doi.org/10.1002/humu.21120. |
| [2] |
Taylor AM, Wlodarski B, Prior IA, et al. Ultrastructural examination of tissue in a patient with alkaptonuric arthropathy reveals a distinct pattern of binding of ochronotic pigment. Rheumatology. 2010;49:1412-1414. https://doi.org/10.1093/rheumatology/keq027. |
| [3] |
Phornphutkul C, Anderson P, Huizing M, et al. Natural history of alkaptonuria. N Engl J Med. 2002;347(26):2111-2121. https://doi.org/10.1056/NEJMoa021736. |
| [4] |
Башкова И.Б., Кичигин В.А., Шаипов Р.Ш., и др. Охроноз как причина вторичного остеоартроза // Русский медицинский журнал. ― 2017. ― Т.25. ― №7. ― С. 474−480. [Bashkova IB, Kichigin VA, Shaipov RSh., et al. Okhronoz kak prichina vtorichnogo osteoartroza. Russkiy meditsinskiy zhurnal. 2017;25(7):474-480. (In Russ.)] |
| [5] |
Perry MB, Suwannarat P, Furst GP, et al. Musculoskeletal findings and disability in alkaptonuria. J Rheumatol. 2006;33(11):2280-2285. |
| [6] |
Ranganath LR, Milan AM, Hughes AT, et al. Suitability of nitisinone in alkaptonuria 1 (SONIA 1): an international, multicentre, randomised, open-label, no-treatment controlled, parallel-group, dose-response study to investigate the effect of once daily nitisinone on 24-h urinary homogentisic acid excretion in patients with alkaptonuria after 4 weeks of treatment. Ann Rheum Dis. 2016;75:362-367. https://doi.org/10.1136/annrheumdis-2014-206033. |
| [7] |
Carrier DA, Harris CM. Bilateral hip and bilateral knee arthroplasties in a patient with ochronotic arthropathy. Orthop Rev. 1990;19(11):1005-1009. |
| [8] |
Peretz A, Dupont M, Famaey JP. Ochronosis: a case report with severe ochronotic arthropathy. Clin Rheumatol. 1983 Sep;2(3):293-8. https://doi.org/10.1007/BF02041405 |
| [9] |
Ventura-Ríos L, Hernández-Díaz C, Gutiérrez-Pérez L, et al. Ochronotic arthropathy as a paradigm of metabolically induced degenerative joint disease. A case-based review. Clin Rheumatol. 2016;35(5):1389-1395. https://doi.org/10.1007/s10067-014-2557-7. |
| [10] |
Doganavsargil B, Pehlivanoglu B, Bicer EK, et al. Black joint and synovia: Histopathological evaluation of degenerative joint disease due to ochronosis. Pathol Res Pract. 2015;211(6):470-477. https://doi.org/10.1016/j.prp.2015.03.001. |
| [11] |
Saigal R, Tank ML, Pathak P, et al. Alkaptonuric ochronosis. J Assoc Physicians India. 2016;64(4):79-80. |
| [12] |
Zmerly H, Moscato M, Di Gregori V. Arthroplasty in alkaptonuric ochronosis. J Popul Ther Clin Pharmacol. 2019;26(2):e20-e24. https://doi.org/10.15586/jptcp.v26i2.624. |
| [13] |
Sabater M, Alías A, Segur JM. Total knee prosthesis in a patient diagnosed with ochronotic arthropathy. Rev Esp Cir Ortop Traumatol. 2020;S1888-4415(20)30013-8. https://doi.org/10.1016/j.recot.2020.01.005. |
| [14] |
Rajkumar N, Soundarrajan D, Dhanasekararaja P, Rajasekaran S. Clinical and radiological outcomes of total joint arthroplasty in patients with ochronotic arthropathy. Eur J Orthop Surg Traumatol. 2020;30(5):923-929. https://doi.org/10.1007/s00590-020-02651-0. |
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