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1.

Заглавие журнала :Экспериментальная онкология -2017г. т.39,N 1
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Auzina D. Prognostic value of the bone turnover markers in multiple myeloma/ D. Auzina, R. Erts, S. Lejniece (стр.53-56)
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2.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Auzina D., Erts R., Lejniece S.
Заглавие : Prognostic value of the bone turnover markers in multiple myeloma
Место публикации : Experimental Oncology. - К., 2017. - Том 39, N 1. - С. 53-56: табл. (Шифр ЕУ12/2017/39/1)
Примечания : 25 ref.
MeSH-главная: МИЕЛОМА МНОЖЕСТВЕННАЯ -- MULTIPLE MYELOMA
Аннотация: Multiple myeloma (MM) is characterized by osteolytic bone disease resulting from increased osteoclast activity and reduced osteoblast function. Aim: The aim of our research was to determine connection between bone turnover markers and presence of bone lesions, their degree of severity, to monitor MM bone disease and to assess effectiveness of anti-myeloma treatment. Materials and Methods: Serum samples and clinical data from 123 patients with newly diagnosed MM were collected at Riga East Clinical University Hospital (Riga, Latvia) from June 2014 to June 2016. Bone lesions detected by radiography, CT scans, MRI, and PET/CT were divided into degrees from 0 to 3 (0 — no bone involvement, 1 — ≤ 3 bone lesions, 2 — ≥ 3 bone lesions, 3 — fracture). Staging was performed applying Durie/Salmon (DS) and International Staging System classifications. Progressive disease was defined as development of one or more new bone lesions. The levels of bone metabolic markers β-isomerized C-terminal telopeptide of collagen type I (β-CTX) and bone-specific alkaline phosphatase (bALP) were monitored regularly in the year. Results: Bone lesions were found in 86 (69%) patients. From these 6 (4%) patients had 1st degree, 11 (9%) had 2nd degree and 69 (56%) had 3rd degree bone lesions. Level of the bone resorption marker β-CTX in the control group was 0.41 ng/ml, which is lower than in MM patients (p 0.001). Spearman correlation coefficient analysis found a positive and statistically significant correlation (rs 0.05). However, β-CTX was found to be an excellent diagnostic marker for MM (AUC 0.91; 95% confidence interval, 0.88–0.94; p 0.001). Conclusions: Patients with MM and bone lesions have increased value of bone resorption marker β-CTX. There is a correlation between bone resorption marker and degree of bone lesions. Changes in β-CTX levels may be used to monitor the effectiveness of myeloma treatment
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