Department of Public Health, Academic Medical Centre, I. van Valkengoed, Meibergdreef 9, J2-209, 1105 AZ, Amsterdam, The Netherlands.
Department of Medical Biochemistry, Academic Medical Centre, I. van Valkengoed, Meibergdreef 9, J2-209, 1105 AZ, Amsterdam, The Netherlands.
Nutr Diabetes. 2017 Dec 19;7(12):300. doi: 10.1038/s41387-017-0003-z.
Accumulation of metabolites may mark or contribute to the development of type 2 diabetes mellitus (T2D), but there is a lack of data from ethnic groups at high risk. We examined sphingolipids, acylcarnitines and amino acids, and their association with T2D in a nested case-control study among 54 South Asian Surinamese, 54 African Surinamese and 44 Dutch in the Netherlands. Plasma metabolites were determined at baseline (2001-2003), and cumulative prevalence and incidence of T2D at follow-up (2011-2012). Weighted linear and logistic regression analyses were used to study associations. The mean level of most sphingolipids was lower, and amino-acid levels higher, in the Surinamese groups than among the Dutch. Surinamese individuals had higher mono- and polyunsaturated acylcarnitines and lower plasma levels of saturated acylcarnitine species than the Dutch. Several sphingolipids and amino acids were associated with T2D. Although only the shorter acylcarnitines seemed associated with prevalent T2D, we found an association of all acylcarnitines (except C0, C18 and C18:2) with incident T2D. Further analyses suggested a potentially different association of several metabolites across ethnic groups. Extension and confirmation of these findings may improve the understanding of ethnic differences and contribute to early detection of increased individual risk.
代谢产物的积累可能标志着 2 型糖尿病(T2D)的发生或与之相关,但在高风险种族群体中缺乏相关数据。我们在荷兰的一项巢式病例对照研究中,对 54 名南亚苏里南人、54 名非洲苏里南人和 44 名荷兰人进行了鞘脂、酰基肉碱和氨基酸检测,并研究了它们与 T2D 的相关性。在基线(2001-2003 年)时测定了血浆代谢物,在随访时(2011-2012 年)测定了 T2D 的累积患病率和发病率。采用加权线性和逻辑回归分析来研究相关性。与荷兰人相比,大多数鞘脂的平均水平在苏里南人群中较低,而氨基酸水平较高。与荷兰人相比,苏里南个体的单不饱和和多不饱和酰基辅酶 A 以及饱和酰基辅酶 A 种类的血浆水平较低。几种鞘脂和氨基酸与 T2D 相关。尽管只有较短的酰基辅酶 A 似乎与现患 T2D 相关,但我们发现所有酰基辅酶 A(除 C0、C18 和 C18:2 外)均与新发 T2D 相关。进一步的分析表明,几种代谢物在不同种族群体中的相关性可能存在差异。扩展和确认这些发现可能有助于更好地了解种族差异,并有助于早期发现个体风险增加。