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Pismo Towarzystwa Internistów Polskich, założone przez prof. Władysława Antoniego Gluzińskiego
Pismo indeksowane w:
MEDLINE/Index Medicus,
EMBASE/Excerpta Medica Database,
Index Copernicus (IC), KBN/MNiSW,
Polish Medical Library (GBL), EBSCO,
ISI Science Citation Index Expanded,
Scopus,
Directory of Open Access Journals (DOAJ)
Wartość Index Copernicus (IC) za 2010: 9 pkt,
punktacja MNiSW: 9 pkt.
Czasopismo dofinansowywane przez MNiSW w ramach działalności wspomagającej badania.
Polskie Archiwum Medycyny Wewnętrznej jest czasopismem typu "open-access" i gwarantuje darmowy dostęp do pełnej treści artykułów.
Dominika Wcisło‑Dziadecka, Anna Kotulska, Ligia Brzezińska‑Wcisło, Eugeniusz J. Kucharz, Anna Lis‑Święty, Grażyna Kamińska‑Wiciorek
Abstrakt
INTRODUCTION: Human cartilage glycoprotein‑39 (HC gp‑39) is a protein secreted by various cells including chondrocytes. Serum HC gp‑39 has been suggested to be a marker of cartilage damage.
However, inflammation involving other sites than the joints is an additional factor that increases the serum level of HC gp‑39.
OBJECTIVES: The aim of the study was to evaluate the usefulness of HC gp‑39 determination in serum of patients with systemic lupus erythematosus (SLE) as a marker of joint involvement.
PATIENTS AND METHODS: Serum HC gp‑39 levels were measured in 25 patients with SLE and 22 healthy controls. SLE activity was assessed by the Systemic Lupus Erythematosus Disease Activity
Index, and articular involvement by calculating the number of swollen and tender joints. The markers of inflammation (erythrocyte sedimentation rate, C‑reactive protein) were determined. RESULTS: We observed an increase in HC gp‑39 in SLE patients. However, there was no correlation of this parameter
with disease activity, inflammatory markers (except serum γ globulin levels), and articular involvement. CONCLUSIONS: The study suggests that increased HC gp‑39 in SLE patients results mainly from inflammation and is not useful as a marker of joint involvement.
Słowa kluczowe
human cartilage glycoprotein‑39, systemic lupus erythematosus
Pol Arch Med Wewn, 2009; 119 (12): 785-788
PMID: 20010462
Pobierz artykuł (PDF): EN abstrakt PL