Bone Mineral Content in Patients with Anaphylactic Reactions, Signs of Mastocytosis and Elevated Basal Serum Tryptase Levels
Introduction: To examine the relationship between elevated basal serum tryptase levels (BST), a marker of total mast cell mass, and bone mineral density (BMD) in patients with anaphylactic reactions and signs of mastocytosis. Methods: Retrospective evaluation of patient charts at an allergy unit. Pa...
Saved in:
Published in | The open allergy journal Vol. 3; no. 1; pp. 7 - 15 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
2010
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Introduction:
To examine the relationship between elevated basal serum tryptase levels (BST), a marker of total mast cell
mass, and bone mineral density (BMD) in patients with anaphylactic reactions and signs of mastocytosis.
Methods:
Retrospective evaluation of patient charts at an allergy unit. Patients with BST levels above 20 ng/ml were eligible
if clinical and follow-up data and results of dual X-ray absorptiometry (DXA) were available. Patients with previous
use of anti-osteoporotic medications and with osteoporosis not caused by mastocytosis were excluded. Spearman’s rank
correlation, Mann-Whitney test and receiver operating characteristic curve (ROC) was used for analysis.
Results:
24 patients were included. The main presenting symptom (17 of 24 patients) was anaphylactic reactions to insect
stings. BST levels ranged between 21 and 158 ng/ml (median 48 ng/ml). Study participants with Z-score values below -
1.0 had a median BST level of 46 ng/ml, the patients with Z-score values above or equal to -1.0 had a median BST level
of 27 ng/ml. ROC analysis of the patient group with BST values between 30 and 100 ng/ml revealed a best cut-off value
of BST to detect a low BMD when BST level would be at least 27 ng/ml resulting in a sensitivity of 92% and a specificity
of 70%.
Conclusion:
Patients with moderately elevated BST levels seem to be at increased risk for low BMD. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1874-8384 1874-8384 |
DOI: | 10.2174/1874838401003010007 |