Low bone mass density is associated with hemolysis in brazilian patients with sickle cell disease

被引:30
作者
Baldanzi, Gabriel [1 ]
Traina, Fabiola [1 ]
Marques Neto, Joao Francisco [3 ]
Santos, Allan Oliveira [2 ]
Ramos, Celso Dario [2 ]
Olalla Saad, Sara T. [1 ]
机构
[1] Univ Estadual Campinas, Hematol & Hemotherapy Ctr, Inst Nacl Ciencia & Tecnol Sangue, Campinas, Brazil
[2] Univ Estadual Campinas, Dept Radiol, Campinas, Brazil
[3] Univ Estadual Campinas, Dept Internal Med, Campinas, Brazil
基金
巴西圣保罗研究基金会;
关键词
Osteoporosis; Sickle Cell Disease; Hemolysis; Bone Mass Density; Kidney; CHRONIC KIDNEY-DISEASE; MINERAL DENSITY; ADULTS; CHILDREN; ANEMIA;
D O I
10.1590/S1807-59322011000500015
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVES: To determine whether kidney disease and hemolysis are associated with bone mass density in a population of adult Brazilian patients with sickle cell disease. INTRODUCTION: Bone involvement is a frequent clinical manifestation of sickle cell disease, and it has multiple causes; however, there are few consistent clinical associations between bone involvement and sickle cell disease. METHODS: Patients over 20 years of age with sickle cell disease who were regularly followed at the Hematology and Hemotherapy Center of Campinas, Brazil, were sorted into three groups, including those with normal bone mass density, those with osteopenia, and those with osteoporosis, according to the World Health Organization criteria. The clinical data of the patients were compared using statistical analyses. RESULTS: In total, 65 patients were included in this study: 12 (18.5%) with normal bone mass density, 37 (57%) with osteopenia and 16 (24.5%) with osteoporosis. Overall, 53 patients (81.5%) had bone mass densities below normal standards. Osteopenia and osteoporosis patients had increased lactate dehydrogenase levels and reticulocyte counts compared to patients with normal bone mass density (p < 0.05). Osteoporosis patients also had decreased hemoglobin levels (p < 0.05). Hemolysis was significantly increased in patients with osteoporosis compared with patients with osteopenia, as indicated by increased lactate dehydrogenase levels and reticulocyte counts as well as decreased hemoglobin levels. Osteoporosis patients were older, with lower glomerular filtration rates than patients with osteopenia. There was no significant difference between the groups with regard to gender, body mass index, serum creatinine levels, estimated creatinine clearance, or microalbuminuria. CONCLUSION: A high prevalence of reduced bone mass density that was associated with hemolysis was found in this population, as indicated by the high lactate dehydrogenase levels, increased reticulocyte counts and low hemoglobin levels.
引用
收藏
页码:801 / 805
页数:5
相关论文
共 29 条
[1]
Sickle cell bone disease: Response to vitamin D and calcium [J].
Adewoye, Adeboye H. ;
Chen, Tai C. ;
Ma, Qianli ;
McMahon, Lillian ;
Mathieu, Jeff ;
Malabanan, Alan ;
Steinberg, Martin H. ;
Holick, Michael F. .
AMERICAN JOURNAL OF HEMATOLOGY, 2008, 83 (04) :271-274
[2]
Al-Elq AH, 2008, SAUDI MED J, V29, P980
[3]
Bone involvement in sickle cell disease [J].
Almeida, A ;
Roberts, I .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 129 (04) :482-490
[4]
[Anonymous], 1994, World Health Organ Tech Rep Ser, V843, P1
[5]
51Cr-EDTA measurements of the glomerular filtration rate in patients with sickle cell anaemia and minor renal damage [J].
Barros, Fabiana B. ;
Lima, Carmen S. P. ;
Santos, Allan O. ;
Mazo-Ruiz, Mariana F. C. ;
Lima, Mariana C. L. ;
Etchebehere, Elba C. S. C. ;
Costa, Fernando F. ;
Saad, Sara T. O. ;
Camargo, Edwaldo E. ;
Ramos, Celso D. .
NUCLEAR MEDICINE COMMUNICATIONS, 2006, 27 (12) :959-962
[6]
Brinker M R, 1998, Am J Orthop (Belle Mead NJ), V27, P43
[7]
Cytokines and plasma factors in sickle cell disease [J].
Brittain, Julia E. ;
Parise, Leslie V. .
CURRENT OPINION IN HEMATOLOGY, 2007, 14 (05) :438-443
[8]
Figueiredo MS, 1996, AM J HEMATOL, V53, P72, DOI 10.1002/(SICI)1096-8652(199610)53:2<72::AID-AJH3>3.0.CO
[9]
2-0
[10]
Nitric oxide therapy in sickle cell disease [J].
Gladwin, MT ;
Schechter, AN .
SEMINARS IN HEMATOLOGY, 2001, 38 (04) :333-342