Ny markør ved trombotisk trombocytopenisk purpura
(2008) In Ugeskrift for Laeger 170(33). p.9-2446- Abstract
Thrombotic microangiopathy can be caused by several conditions which are difficult to diagnose from the clinical presentation alone. Deficient enzyme activity of a newly-discovered enzyme, ADAMTS-13, can lead to thrombotic thrombocytopenic purpura (TTP). Lack of ADAMTS-13 activity causes increased concentrations of high molecular weight von Willebrand factor forms and increased platelet aggregation. Measurement of ADAMTS-13 activity is useful for the diagnosis of TTP and may also be relevant as a prognostic test for recurrent TTP.
- Abstract (Swedish)
- Der findes flere trombotiske mikroangiopatier, som kan være
svære at adskille ud fra den kliniske præsentation. Mangel på et
nyopdaget enzym, a disintegrin and metalloprotease with throm-
bospondin type 1 motifs (ADAMTS)-13, kan forårsage trombotisk
trombocytopenisk purpura (TTP). Mangel på ADAMTS-13 fører til
øgede koncentrationer af højmolekylære von Willebrand-faktor-
former i plasma og fremmer dannelse af trombose i mikrovasku-
laturen. ADAMTS-13-mangel kan være arvelig eller erhvervet. Nye
metoder til bestemmelse af ADAMTS-13-aktivitet i plasma kan
bidrage i den diagnostiske proces ved mistanke om TTP
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/c519a1c7-8c3f-427f-b5e5-794b17d94276
- author
- Gøtze, Jens Peter ; Hillarp, Andreas LU ; Lindblom, Anders ; Björk, Peter LU ; Strandberg, Karin LU and Nielsen, Lars Bo LU
- organization
- alternative title
- New marker in thrombotic thrombocytopenic purpura
- publishing date
- 2008-08-11
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- ADAM Proteins/blood, ADAMTS13 Protein, Biomarkers/blood, Diagnosis, Differential, Humans, Purpura, Thrombotic Thrombocytopenic/blood, von Willebrand Factor/genetics
- in
- Ugeskrift for Laeger
- volume
- 170
- issue
- 33
- pages
- 4 pages
- publisher
- Almindelige Danske Laegeforening
- external identifiers
-
- pmid:18761827
- scopus:49949097955
- ISSN
- 0041-5782
- language
- Danish
- LU publication?
- yes
- id
- c519a1c7-8c3f-427f-b5e5-794b17d94276
- alternative location
- https://ugeskriftet.dk/files/scientific_article_files/2013-11//artikel_3626.pdf
- date added to LUP
- 2022-08-29 10:12:35
- date last changed
- 2025-10-14 12:32:31
@article{c519a1c7-8c3f-427f-b5e5-794b17d94276,
abstract = {{<p>Thrombotic microangiopathy can be caused by several conditions which are difficult to diagnose from the clinical presentation alone. Deficient enzyme activity of a newly-discovered enzyme, ADAMTS-13, can lead to thrombotic thrombocytopenic purpura (TTP). Lack of ADAMTS-13 activity causes increased concentrations of high molecular weight von Willebrand factor forms and increased platelet aggregation. Measurement of ADAMTS-13 activity is useful for the diagnosis of TTP and may also be relevant as a prognostic test for recurrent TTP.</p>}},
author = {{Gøtze, Jens Peter and Hillarp, Andreas and Lindblom, Anders and Björk, Peter and Strandberg, Karin and Nielsen, Lars Bo}},
issn = {{0041-5782}},
keywords = {{ADAM Proteins/blood; ADAMTS13 Protein; Biomarkers/blood; Diagnosis, Differential; Humans; Purpura, Thrombotic Thrombocytopenic/blood; von Willebrand Factor/genetics}},
language = {{dan}},
month = {{08}},
number = {{33}},
pages = {{9--2446}},
publisher = {{Almindelige Danske Laegeforening}},
series = {{Ugeskrift for Laeger}},
title = {{Ny markør ved trombotisk trombocytopenisk purpura}},
url = {{https://ugeskriftet.dk/files/scientific_article_files/2013-11//artikel_3626.pdf}},
volume = {{170}},
year = {{2008}},
}