Document Detail

Mild hyperhomocysteinemia in adult patients with sickle cell disease: a common finding unrelated to folate and cobalamin status.
MedLine Citation:
PMID:  15164375     Owner:  NLM     Status:  MEDLINE    
Homocysteine has associations with both vitamin insufficiency and vascular complications, and its status is therefore of interest in sickle cell disease (SCD). However, information is limited, especially in adults. We studied plasma total homocysteine (tHcy) and three of its major modifiers, cobalamin, folate, and creatinine, in 90 adult patients with SCD and 76 control subjects. The patients had higher tHcy levels than did controls (P = 0.03) and had elevated tHcy more often (20% vs. 3%, P = 0.0005). None of the hyperhomocysteinemic patients had low cobalamin or folate levels; on the contrary, patients with SCD had high folate levels more often than control subjects (32% vs. 7%; P < 0.0001). Although serum creatinine values were lower in SCD patients than in control subjects (P = 0.03), high levels also tended to occur more often (8% vs. 1%; P = 0.054). Most importantly, creatinine levels correlated significantly with tHcy (P < 0.0001) and logistic regression analyses showed creatinine to be the only significant predictor of high tHcy levels in SCD (P = 0.01). Our results show that hyperhomocysteinemia affects 20% of adults with SCD despite routine folate supplementation and is independent of folate and cobalamin status. Creatinine was the major identifiable influence on tHcy, but renal insufficiency explained only 4 of the 18 elevated tHcy levels. Longitudinal studies will be needed to determine whether the frequent hyperhomocysteinemia of SCD influences the vascular complications in SCD. If reducing tHcy becomes advisable, then interventions other than folate therapy will be needed.
Meekoo Dhar; Rita Bellevue; Shabneet Brar; Ralph Carmel
Related Documents :
3408135 - Elective splenectomy in haematological disorders.
7577635 - Splenic irradiation for chronic autoimmune thrombocytopenic purpura in patients with co...
6414355 - Clomiphene-responsive hypogonadism in sickle cell anemia.
9542685 - Alternative approaches to the management of priapism.
6170755 - Inosiplex: a novel treatment in rheumatoid arthritis?
24045265 - Diagnostic role of computed tomographic enterography differentiating crohn disease from...
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  American journal of hematology     Volume:  76     ISSN:  0361-8609     ISO Abbreviation:  Am. J. Hematol.     Publication Date:  2004 Jun 
Date Detail:
Created Date:  2004-05-27     Completed Date:  2004-07-12     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  7610369     Medline TA:  Am J Hematol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  114-20     Citation Subset:  IM    
Copyright Information:
Copyright 2004 Wiley-Liss, Inc.
Department of Medicine, New York Methodist Hospital, Brooklyn, New York 11215, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Anemia, Sickle Cell / blood*,  complications*
Creatinine / blood
Folic Acid / blood*
Hemoglobin SC Disease / blood
Hyperhomocysteinemia / blood*,  complications
Middle Aged
Regression Analysis
Reproducibility of Results
Vitamin B 12 / blood*
Grant Support
Reg. No./Substance:
59-30-3/Folic Acid; 60-27-5/Creatinine; 68-19-9/Vitamin B 12

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Use of alveolar carbon monoxide to measure the effect of ribavirin on red blood cell survival.
Next Document:  Determinants of ELISA D-dimer sensitivity for unstable angina pectoris as defined by coronary cathet...