Orak Hücreli Anemi'de Kemik Yoğunluk Anomalileri ve İlişkili Faktörler
AMAÇ: Orak hücreli anemi (OHA)'de osteopeni ve osteoporoz riski net olarak ortaya konmamıştır. Bu çalışmada OHA hastalarımızda anormal kemik yoğunluğu sıklığını ve bunun klinik/laboratuvar bulgularla olan ilişkisini saptamayı amaçladık. YÖNTEMLER: Çalışmamıza hemoglobinopati merkezimize rutin kontrole gelen, vazookluziv krizi olmayan OHA hastalarını aldık. Kemik mineral yoğunluğu (KMY) "dual energy xrayabsorbtiometry (DEXA)" kullanılarak spinal kolon ve proksimal femurdan ölçüldü. Osteopeni ve osteoporoz WHO kriterlerine göre değerlendirildi. BULGULAR: Altmış üç hastanın sonuçları değerlendirildi. Hastalarda %39,7 oranında osteopeni, %36,5 osteoporoz ve %23,8 normal KMY bulundu. Anormal KMY ile hemoglobin, lökosit, laktat dehidrogenaz, total bilirubin, ürik asit, alkalen fosfataz ve vitamin B12 düzeyleri arasında ilişki bulunamadı. SONUÇ: Bu çalışmaya göre osteopeni ve osteoporoz OHA hastalarında sıktır. Klinisyenler osteoporoz hakkında dikkatli olmalı ve bu hastalar kırıklardan korunmak için KMY ölçümleri ile izlenmelidir
Bone Density Abnormalities and Related Factors in Sickle Cell Anemia
OBJECTIVE: The risk of osteopenia and osteoporosis has not been clearly found in sickle cell anemia (SCA) patients. In this study, we aimed to find the frequency of abnormal bone mineral density and determine the relationship of abnormal BMD with clinical/laboratuary findings of our SCA patients. METHODS: We added sickle cell anemia patients without vasooclusive crisis during rutine control in our hemoglobinopahy center. Bone mineral danistometry measurements were done with dual energy xrayabsorbtiometry (DEXA) at lumbar spinal colon and proximal femur regions. Osteopenia and osteoporosis were evaluated according to WHO criteria. RESULTS: We evaluated 63 patients' results. There were 39,7% osteopenia, 36,5% osteoporosis, 23,8% normal BMD. There was no relationship among abnormal BMD with hemoglobin, leukocyte, lactate dehydrogenase, total bilirubin, uric acid, alkaline phosphatase and vitamin B12 levels. CONCLUSION: According to our study, osteopenia and osteoporosis are frequent in our SCA patients. Clinicians sould be careful about osteoporosis and these patients should be screen with BMD measurements for avoiding fractures
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- AH Adewoye, TC Chen, Q Ma et al. Sickle cell bone disease: Response to vitamin D and calcium. Am J of Hematol 2007;83:271-4.
- M Sadat-Ali, A Al-Elq, O Sultan et al. Secondary osteoporosis due to sickle cellanemia do sex steroids pla a role? Indian J Med Sci2008;62:193-8. 3. G Baldanzi, F Traina , JF Marques Neto et al . Low bone mass density is associated with hemolysis in Brazilian patients with sickle cell disease. Clinics (Sao Paulo)2011;66:801-5.
- M Sarrai, H Duroseau, J D'Augustine, et al. Bone mass density in adults with sickle cell disease. Br J Haematol2007;136:666-72.
- FT Shah, R Chatterjee, M Owusu-Asante et al. Adults with Severe Sickle Cell Anaemia and Iron Overload Have a High Incidence of Osteopenia and Osteoporosis. Abstracts) 2004 104: Abstract 1684.
- Elshal MF, AEBernawi, MA Al-Ghamdy et al. The association of bone mineral density and parathyroid hormone with serum magnesium in adult patients with sickle-cell anaemia. Med Sci2012; 8: 270-276.
- S Ozen, S Unal, S Erçetin et al. Frequency and endocrine complications of Turkish children and adolescents with sickle cell anemia. Turk J Haematol 2013;30:25-31. Annual Meeting