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논문 기본 정보

자료유형
학술저널
저자정보
Jong Dae Kim (Daegu Haany University) Mi Yeon Park (Daegu Haany University) Joo Wan Kim (Techno Park Marine Bio-industry Development Center) Ki Young Kim (Techno Park Marine Bio-industry Development Center) Hyung Rae Cho (Techno Park Marine Bio-industry Development Center) In Soon Choi (Silla University) Jae Suk Choi (Silla University) Sae Kwang Ku (Daegu Haany University) Soo-Jin Park (Daegu Haany University)
저널정보
한의병리학회 동의생리병리학회지 동의생리병리학회지 제29권 제4호
발행연도
2015.8
수록면
330 - 336 (7page)
DOI
10.15188/kjopp.2015.08.29.4.330

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초록· 키워드

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Polycan originating from Aureobasidium pullulans is mostly composed of β-1, 3/1, 6 glucans and possesses an anti-osteoporotic effect. We conducted a randomized, double-blind, placebo-controlled trial to examine the efficacy and safety of the polycan on bone biochemical markers in healthy perimenopausal women. Sixty subjects were randomly allocated to 2 groups?group 1 received 400 mg of polycan and group 2 received placebo?these were administered once daily for 28 days. Fasting blood and urine samples were collected at baseline and 4 weeks after treatment. The primary outcome was change in osteocalcin (OSC) and bone-specific alkaline phosphatase (BALP). Changes in calcium (Ca), phosphorus (P), C-telopeptide of collagen cross-links (CTx), N-telopeptide of collagen cross-links (NTx), and deoxypyridinoline (DPYR) were the secondary outcomes. A safety assessment was performed using adverse event (AE) and laboratory data. After 4 weeks of polycan treatment, OSC, DPYR, and BALP levels changed (P < 0.05) significantly from baseline in both groups. However, no significant differences were observed in any markers between the 2 groups, except for P (P < 0.05). Interestingly, group 2 showed a significant increase in CTx (65.2%, P < 0.05), while CTx in group 1 slightly increased (17.2%). Both groups showed no significant differences in AE. Although 4 weeks of polycan treatment did not have a statistically significant effect on bone metabolism biomarkers, increases in CTx were modestly inhibited by polycan. Further studies in a large population and longer treatment periods are needed to confirm the effect of polycan on bone turnover.

목차

Introduction
Materials and Methods
Results
Discussion
References

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