1] Department of Internal Medicine, Institute for Cardiovascular Research (ICaR-VU), VU University Medical Center Amsterdam, The Netherlands [2] Faculty of Earth and Life Sciences, Department of Health Sciences, EMGO+ Institute for Health and Care Research, VU University Amsterdam, The Netherlands.
Nutr Diabetes. 2013 Sep 30;3(9):e90. doi: 10.1038/nutd.2013.31.
Although body fat and body fat distribution are known to be related to cardiovascular diseases (CVDs), it is unknown whether specific 30-year developmental patterns of body fat are associated with CVDs. This study examines the existence of distinct developmental patterns of total fat measured by the sum of four skinfolds (S4SFs) and body fat distribution measured by the skinfold thickness ratio (SFratio), and relates these patterns to micro- and macrovascular functions.
In 2006, 259 apparently healthy subjects were examined on micro- and macrovascular functions, using video microscopy and carotid ultrasound sonography. Body fat, using both S4SFs and SFratio, was measured for 10 times over 30 years, from 13 years onwards. Latent class growth analyses (LCGA) were used to obtain distinct developmental patterns of S4SFs and SFratio. This is a data-drive hypothesis-generating approach and could possibly give a new perspective on body fatness over time. In addition, a mixed-method approach is used to obtain individual growth parameters. Linear regression analyses were used to examine the relationship of these patterns and individual growth parameters with micro- and macrovascular functions.
LCGA identified normal and unfavourable developmental patterns in S4SFs and SFratio. Both men and women with an unfavourable developmental pattern of S4SFs showed impaired carotid compliance (β=-0.216, P=0.004 and β=-0.109, P=0.039, respectively), carotid distensibility (β=-5.078, P=0.001 and β=-5.118, P<0.001, respectively) and Young's elastic modulus (β=0.066, P=0.065 and β=0.107, P<0.001, respectively). In contrast, no relationship for microvascular function with developmental patterns of S4SFs was found. Developmental patterns of the SFratio were associated with neither measures of micro- nor macrovascular functions. No associations were using the individual growth parameters.
For macrovascular function, there is a relationship of 30-year developmental patterns of S4SFs, whereas no such relationship was found for the 30-year developmental patterns of S4SFs or SFratio with microvascular function.
虽然体脂和体脂分布与心血管疾病(CVDs)有关,但尚不清楚特定的 30 年体脂发展模式是否与 CVDs 有关。本研究探讨了通过四个皮褶(S4SFs)总和测量的总脂肪和通过皮褶厚度比(SFratio)测量的体脂分布的不同发展模式的存在,并将这些模式与微血管和大血管功能相关联。
2006 年,对 259 名看似健康的受试者进行了微血管和大血管功能检查,使用视频显微镜和颈动脉超声检查。从 13 岁开始,在 30 年内进行了 10 次体脂测量,使用 S4SFs 和 SFratio。使用潜在类别增长分析(LCGA)获得 S4SFs 和 SFratio 的不同发展模式。这是一种数据驱动的假设生成方法,可能会为随着时间的推移体脂提供新的视角。此外,还使用混合方法来获得个体生长参数。线性回归分析用于检查这些模式和个体生长参数与微血管和大血管功能的关系。
LCGA 确定了 S4SFs 和 SFratio 的正常和不利的发展模式。S4SFs 发展模式不佳的男性和女性颈动脉顺应性均受损(β=-0.216,P=0.004 和 β=-0.109,P=0.039),颈动脉可扩展性(β=-5.078,P=0.001 和 β=-5.118,P<0.001)和杨氏弹性模量(β=0.066,P=0.065 和 β=0.107,P<0.001)。相比之下,未发现 S4SFs 发展模式与微血管功能之间存在关系。SFratio 的发展模式与微血管和大血管功能的任何指标均无关联。个体生长参数也没有关联。
对于大血管功能,存在 S4SFs 的 30 年发展模式的关系,而对于 S4SFs 或 SFratio 的 30 年发展模式与微血管功能没有这样的关系。