Bone Status in Patients with Sickle Cell Disease: A Case Control Study

作者: Bassem S. El Deek

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摘要: Objectives (background): Both sickle cell disease and vitamin D deficiency are common among Saudi population. The present work asses Parathyroid hormone/Vitamin axis as well bone dynamics in young adults with disease.Methods: A case control study includes forty patients known to have from the outpatient clinics of North Western Armed Forces Hospital, Tabuk were randomly selected for study. Another 120 healthy individuals involved control. Cases subjected full history taking, clinical examination, radiologic laboratory investigations.Results: Bone image revealed diffuse osteopenia 16 (40%) cases, avascular necrosis femoral head 6 (15%), code fish vertebral bodies (15%) coarse trabecular pattern (15%). Laboratory investigations hypocalcemia 18 (45%), secondary hyperparathyroidism 24 (60%), non-detectable 30 (75%) detectable but subnormal 10 (25%). mean level serum calcium cases was significantly less than that (p < 0.001).. intact hormone higher 0.001). Serum 25-hydroxyvitamin lower studied For Specific Alkaline Phosphatase 0.001).Conclusion: Vitamin though a finding it is more severe subsequent frequent hypocalcemia.

参考文章(15)
Robert P. Hebbel, Stephen H. Embury, Sickle Cell Disease: Basic Principles and Clinical Practice ,(1994)
Antonio Almeida, Irene Roberts, Bone involvement in sickle cell disease. British Journal of Haematology. ,vol. 129, pp. 482- 490 ,(2005) , 10.1111/J.1365-2141.2005.05476.X
Dawn Smiley, Samuel Dagogo-Jack, Guillermo Umpierrez, Therapy insight: metabolic and endocrine disorders in sickle cell disease. Nature Clinical Practice Endocrinology & Metabolism. ,vol. 4, pp. 102- 109 ,(2008) , 10.1038/NCPENDMET0702
Gregory J. Kato, Mark T. Gladwin, Martin H. Steinberg, Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes Blood Reviews. ,vol. 21, pp. 37- 47 ,(2007) , 10.1016/J.BLRE.2006.07.001
Adeboye H. Adewoye, Tai C. Chen, Qianli Ma, Lillian McMahon, Jeff Mathieu, Alan Malabanan, Martin H. Steinberg, Michael F. Holick, Sickle cell bone disease: response to vitamin D and calcium. American Journal of Hematology. ,vol. 83, pp. 271- 274 ,(2008) , 10.1002/AJH.21085
Redonda G Miller, Jodi B Segal, Bimal H Ashar, Sophia Leung, Shamim Ahmed, Shabina Siddique, Tasha Rice, Sophie Lanzkron, None, High prevalence and correlates of low bone mineral density in young adults with sickle cell disease American Journal of Hematology. ,vol. 81, pp. 236- 241 ,(2006) , 10.1002/AJH.20541
Alisha J. Rovner, Virginia A. Stallings, Deborah A. Kawchak, Joan I. Schall, Kwaku Ohene-Frempong, Babette S. Zemel, High risk of vitamin D deficiency in children with sickle cell disease. Journal of The American Dietetic Association. ,vol. 108, pp. 1512- 1516 ,(2008) , 10.1016/J.JADA.2008.06.433
Mir Sadat-Ali, Abdulmoshsen Al-Elq, Osama Sultan, Haifa Al-Turki, Secondary osteoporosis due to sickle cell anemia: do sex steroids play a role? Indian Journal of Medical Sciences. ,vol. 62, pp. 193- 198 ,(2008) , 10.4103/0019-5359.40984
S Mohammed, S Addae, S Suleiman, F Adzaku, S Annobil, O Kaddoumi, J Richards, Serum Calcium, Parathyroid Hormone, and Vitamin D Status in Children and Young Adults with Sickle Cell Disease: Annals of Clinical Biochemistry. ,vol. 30, pp. 45- 51 ,(1993) , 10.1177/000456329303000108
Melissa A. Kacena, Caren M. Gundberg, Mark C. Horowitz, A reciprocal regulatory interaction between megakaryocytes, bone cells, and hematopoietic stem cells Bone. ,vol. 39, pp. 978- 984 ,(2006) , 10.1016/J.BONE.2006.05.019