Medical School, University of Western Australia, Perth, Western Australia, Australia.
Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Perth, Western Australia, Australia.
Intern Med J. 2020 Apr;50(4):460-469. doi: 10.1111/imj.14379.
There is uncertainty over how lean mass, physical activity (PA) and 25-hydroxyvitamin D (25-OH-D) status interact on metabolic syndrome (MetS) risk in adults.
To test the hypothesis that these factors additively influence MetS risk.
Four thousand eight hundred and fifty-eight adults (54.6% female) mean ± SD age 58.0 ± 5.8 years, body mass index 28.1 ± 4.8 kg/m , resident in Busselton, Western Australia. PA assessed by questionnaire (all/total and vigorous), lean mass using dual energy X-ray absorptiometry (% total body mass), serum 25-OH-D via immunoassay, analysed using multivariable logistic regression.
In men, lower total PA was associated with MetS (no vs >24 h/week odds ratio (OR) = 3.1; ≤8 vs >24 h/week OR = 1.8, both P < 0.001), as was lower lean mass (low vs high OR = 20.4; medium vs high OR = 7.4, both P < 0.001). Men with low lean mass exhibited a U-shaped relationship of vigorous PA with MetS risk (covariate-adjusted: 0 vs 4-8 h/week OR = 2.1, P = 0.037; >12 vs 4-8 h/week OR = 4.3, P = 0.002; interaction P = 0.039). In women, low PA (0 vs >24 h/week OR = 2.1, P = 0.003) and lean mass (low vs high OR = 13.1; medium vs high OR = 7.2, both P < 0.001) were associated with MetS risk. Low 25-OH-D status was associated with MetS in men (low vs high OR = 4.1; medium vs high OR = 2.3, both P < 0.001) and women (OR = 3.5 and 2.1 respectively, both P < 0.001) with no PA interaction.
Men and women with high lean mass have low risk of MetS regardless of PA. Low lean mass identifies men who may benefit most from increasing PA, with an optimal level associated with lowest risk. 25-OH-D and PA do not interact on MetS risk.
目前尚不清楚瘦体重、身体活动(PA)和 25-羟维生素 D(25-OH-D)状态如何共同影响成年人的代谢综合征(MetS)风险。
检验这些因素是否会对 MetS 风险产生累加影响的假设。
本研究共纳入 4858 名成年人(54.6%为女性),平均年龄为 58.0 ± 5.8 岁,平均 BMI 为 28.1 ± 4.8kg/m2,居住在澳大利亚西部的巴斯勒顿。通过问卷调查(所有/总活动和剧烈活动)评估 PA,使用双能 X 射线吸收法(DXA)测量瘦体重(占总体重的百分比),通过免疫测定法检测血清 25-OH-D,采用多变量逻辑回归进行分析。
在男性中,较低的总 PA 与 MetS 相关(无 PA 与每周>24 小时的 OR=3.1;每周≤8 小时与每周>24 小时的 OR=1.8,均 P<0.001),较低的瘦体重也与 MetS 相关(低水平与高水平的 OR=20.4;中水平与高水平的 OR=7.4,均 P<0.001)。瘦体重较低的男性与剧烈 PA 呈 U 形关系与 MetS 风险相关(调整协变量后:0 与 4-8 小时/周的 OR=2.1,P=0.037;>12 与 4-8 小时/周的 OR=4.3,P=0.002;交互作用 P=0.039)。在女性中,较低的 PA(0 与每周>24 小时的 OR=2.1,P=0.003)和瘦体重(低水平与高水平的 OR=13.1;中水平与高水平的 OR=7.2,均 P<0.001)与 MetS 风险相关。男性和女性中低 25-OH-D 状态与 MetS 相关(低水平与高水平的 OR=4.1;中水平与高水平的 OR=2.3,均 P<0.001),且这种相关性不受 PA 的影响。
无论 PA 水平如何,高瘦体重的男性和女性患 MetS 的风险均较低。瘦体重较低的男性可能从增加 PA 中获益最多,且存在一个最佳的 PA 水平,该水平与最低的风险相关。25-OH-D 和 PA 对 MetS 风险没有交互作用。