Dietary Fat Intake and Radiographic Progression of Knee Osteoarthritis: Data From the Osteoarthritis Initiative.
Dietary Fat Intake and Radiographic Progression of Knee Osteoarthritis: Data From the Osteoarthritis Initiative.
复制标题
膳食脂肪摄入与膝关节骨关节炎的放射学进展:来自骨关节炎倡议的数据。
DOI:
10.1002/acr.22952
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发表时间:
2017-03
影响因子:
4.7
通讯作者:
Eaton, Charles B.
中科院分区:
文献类型:
--
作者:
Lu, Bing;Driban, Jeffrey B.;Xu, Chang;Lapane, Kate L.;McAlindon, Timothy E.;Eaton, Charles B.
Few studies have investigated the role of dietary factors on knee osteoarthritis (OA) progression. We examined the prospective association of dietary fat intake with radiographic progression of knee OA. In the Osteoarthritis Initiative, 2092 participants with radiographic knee OA and having baseline dietary data were followed at yearly intervals up to 48 months. Dietary intakes of fatty acids were assessed with the Block Brief Food Frequency Questionnaire. To evaluate radiographic progression of knee OA, we used quantitative joint space width (JSW) between the medial femur and tibia of the knee based on fixed-flexion posterior-anterior radiographs. Linear mixed models for repeated measures were used to test the association between dietary fat and JSW loss over time. We observed significant positive relationships of total fat and saturated fatty acids (SFA) intakes with JSW loss. With increasing quartiles of total fat intake, the JSW decreases over 48 months were 0.26mm, 0.27mm, 0.31mm and 0.35 mm respectively (P trend=0.02). Similar association was observed between SFA intake and JSW loss. In contrast, higher intakes of mono- and poly-unsaturated fatty acids (MUFA, PUFA), and higher ratio of PUFA to SFA were associated with a reduced JSW loss. High intakes of total fat and SFA may be associated with increased structural knee OA progression, while MUFA and PUFA may reduce radiographic progression. Replication of these novel findings in other prospective studies are needed to confirm if reduction in SFA intake and increase in unsaturated fat intake lead to delayed knee OA progression.
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DOI:
10.1016/s0140-6736(14)60613-9
发表时间:
2014-06-07
期刊:
Lancet (London, England)
影响因子:
--
作者:
Ley SH;Hamdy O;Mohan V;Hu FB
通讯作者:
Hu FB
影响因子:
27.4
作者:
Goldring MB;Otero M;Tsuchimochi K;Ijiri K;Li Y
通讯作者:
Li Y
影响因子:
--
作者:
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通讯作者:
Wolfe, Frederick
DOI:
10.1097/00075197-200103000-00006
发表时间:
2001-03-01
影响因子:
3.1
作者:
Calder, PC;Zurier, RB
通讯作者:
Zurier, RB
影响因子:
7
作者:
Brunner, A. M.;Henn, C. M.;Ehrlich, M. G.
通讯作者:
Ehrlich, M. G.