Vadachkoria Surab, Woelk Godfrey B, Mahomed Kassam, Qiu Chunfang, Muy-Rivera Martin, Malinow M Rene, Williams Michelle A
Center for Perinatal Studies (Swedish Medical Center, Seattle, Washington, USA.
Am J Hypertens. 2006 Mar;19(3):235-42. doi: 10.1016/j.amjhyper.2005.08.003.
We examined the relationship of maternal plasma concentrations of soluble vascular cell adhesion molecule-1 (sVCAM-1), a specific marker of endothelial dysfunction, and risk of preeclampsia. We also evaluated the relationship in the presence and absence of maternal hypertriglyceridemia and hyperhomocystein(e)mia.
A total of 170 women with preeclampsia and 184 control subjects were included in this case-control study analysis. Maternal postdiagnosis plasma sVCAM-1 concentrations were determined using immunoassays. Total plasma homocysteine (tHcy) was measured using high-performance liquid chromatography with electrochemical detection procedures; and triglyceride concentrations were determined using standard enzymatic procedures. Logistic regression procedures were used to estimate odds ratios (OR) and 95% confidence intervals (CI) adjusted for confounders.
The relative risk of preeclampsia (as estimated by the OR) was increased 3.6-fold for women with sVCAM-1 concentrations >/=842 ng/mL compared with women who had lower concentrations (OR = 3.6; 95% CI 1.8 to 7.4). Of the three biological markers investigated, elevated sVCAM-1 concentrations was most strongly related to preeclampsia risk (OR = 4.6, 95% CI 1.6 to 13.5), followed by hyperhomocysten(e)mia (OR = 2.4, 95% CI 0.8 to 7.4) and hypertriglyceridemia (OR = 2.1, 95% CI 0.9 to 5.0). Compared with women who did not have any of the three risk factors, those with all three risk factors had an extremely high risk of preeclampsia (OR = 26.4; 95% CI 8.5 to 81.9).
These findings suggest that elevated sVCAM-1 concentrations are associated with an increased risk of preeclampsia. Our findings extend the literature by documenting progressively increased risk with increasing numbers of biological markers of dyslipidemia and endothelial dysfunction.
我们研究了可溶性血管细胞黏附分子-1(sVCAM-1,内皮功能障碍的一种特异性标志物)的母体血浆浓度与先兆子痫风险之间的关系。我们还评估了在存在和不存在母体高甘油三酯血症及高同型半胱氨酸血症的情况下这种关系。
本病例对照研究分析共纳入了170例先兆子痫女性和184例对照对象。采用免疫测定法测定母体诊断后血浆sVCAM-1浓度。使用高效液相色谱电化学检测法测量总血浆同型半胱氨酸(tHcy);并使用标准酶促法测定甘油三酯浓度。采用逻辑回归程序估计经混杂因素校正的比值比(OR)和95%置信区间(CI)。
与sVCAM-1浓度较低的女性相比,sVCAM-1浓度≥842 ng/mL的女性先兆子痫的相对风险(由OR估计)增加了3.6倍(OR = 3.6;95% CI 1.8至7.4)。在研究的三种生物学标志物中,sVCAM-1浓度升高与先兆子痫风险的相关性最强(OR = 4.6,95% CI 1.6至13.5),其次是高同型半胱氨酸血症(OR = 2.4,95% CI 0.8至7.4)和高甘油三酯血症(OR = 2.1,95% CI 0.9至5.0)。与没有这三种危险因素中任何一种的女性相比,具有所有三种危险因素的女性患先兆子痫的风险极高(OR = 26.4;95% CI 8.5至81.9)。
这些发现表明,sVCAM-1浓度升高与先兆子痫风险增加相关。我们的发现通过记录血脂异常和内皮功能障碍的生物学标志物数量增加导致风险逐渐增加,扩展了相关文献。