CNR-IBIM, National Research Council, Institute of Biomedicine, Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension, Reggio Calabria, Italy.
J Hypertens. 2010 Aug;28(8):1745-51. doi: 10.1097/HJH.0b013e32833bd21b.
Neuropeptide Y (NPY) is a sympathetic neurotransmitter that acts on multiple receptors involved in cardiovascular remodelling and angiogenesis. Plasma levels of NPY are increased in patients with end-stage renal disease (ESRD) and are independently related to left ventricular hypertrophy (LVH) and incident cardiovascular events in these patients.
To investigate the relationship between NPY receptor Y2 gene polymorphism and left ventricular mass index (LVMI) as well as the interaction between this polymorphism and plasma NPY in determining LVH in 189 ESRD patients.
LVMI was significantly higher (+12%, P = 0.03) in patients carrying the C allele than in those without C allele and was linearly associated with plasma NPY (P = 0.01). Interaction analysis showed a significant NPY-LVMI relationship in patients with the C allele, both at univariate (r = 0.27, P = 0.001) and multivariate (r = 0.21, P = 0.01) analyses, whereas no such relationship existed in patients without this allele. In fully adjusted analyses, a 10 pmol/l increase in plasma NPY entailed a 4.9 g/m increase in LVMI in patients with C allele, whereas the same change in NPY levels did not modify the NPY-LVMI link in patients without such allele (P = 0.009).
NPY receptor Y2 polymorphism is independently associated with LVMI and interacts with plasma levels of NPY in explaining the variability of LVH in ESRD. These results offer a genetic basis to the hypothesis that NPY is causally implicated in the pathogenetic pathway leading to LVH in ESRD patients.
神经肽 Y(NPY)是一种交感神经递质,作用于多种参与心血管重塑和血管生成的受体。终末期肾病(ESRD)患者的血浆 NPY 水平升高,并且与这些患者的左心室肥厚(LVH)和心血管事件的发生独立相关。
研究 NPY 受体 Y2 基因多态性与左心室质量指数(LVMI)之间的关系,以及这种多态性与血浆 NPY 之间的相互作用在确定 189 例 ESRD 患者的 LVH 中的作用。
携带 C 等位基因的患者的 LVMI 显著升高(+12%,P=0.03),并且与血浆 NPY 呈线性相关(P=0.01)。交互分析显示,携带 C 等位基因的患者中存在显著的 NPY-LVMI 关系,无论是在单变量(r=0.27,P=0.001)还是多变量(r=0.21,P=0.01)分析中,而在没有这种等位基因的患者中则没有这种关系。在完全调整的分析中,血浆 NPY 增加 10 pmol/L,携带 C 等位基因的患者的 LVMI 增加 4.9 g/m,而在没有这种等位基因的患者中,NPY 水平的相同变化并没有改变 NPY-LVMI 之间的联系(P=0.009)。
NPY 受体 Y2 多态性与 LVMI 独立相关,并与血浆 NPY 水平相互作用,解释了 ESRD 患者 LVH 的变异性。这些结果为 NPY 因果参与 ESRD 患者 LVH 发病途径的假设提供了遗传基础。