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非酯化脂肪酸与自发性早产:用于识别风险模式的因素分析

Nonesterified fatty acids and spontaneous preterm birth: a factor analysis for identification of risk patterns.

作者信息

Catov Janet M, Bertolet Marnie, Chen Yi-Fan, Evans Rhobert W, Hubel Carl A

出版信息

Am J Epidemiol. 2014 May 15;179(10):1208-15. doi: 10.1093/aje/kwu037. Epub 2014 Apr 8.

Abstract

We considered that accumulation of nonesterified (free) fatty acids (NEFAs) in the first trimester of pregnancy would mark women at excess risk of spontaneous preterm birth (sPTB) and examined the interplay between NEFAs, lipids, and other markers to explore pathways to sPTB. In a case-control study nested in the Pregnancy Exposures and Preeclampsia Prevention Study (Pittsburgh, Pennsylvania, 1997-2001), we assayed NEFA levels in nonfasting serum collected at a mean gestational week of 9.4 (range, 4-20 weeks) in 115 women with sPTB (<37 weeks) and 222 women with births occurring at ≥37 weeks. C-reactive protein, total cholesterol, low-density lipoprotein and high-density lipoprotein (HDL) cholesterol, triglycerides, and uric acid were also measured. Polytomous logistic regression models were used to evaluate tertiles of NEFA levels and sPTB at <34 weeks and 34-36 weeks; factor analysis was used to characterize patterns of biomarkers. Women with NEFA levels in the highest tertile versus the lowest were 2.02 (95% confidence interval: 1.13, 3.48) times more likely to have sPTB, after adjustment for covariates. Risk of sPTB before 34 weeks was particularly high among women with high NEFA levels (odds ratio = 3.73, 95% confidence interval: 1.33, 10.44). Six biomarker patterns were identified, and 2 were associated with sPTB: 1) increasing NEFA and HDL cholesterol levels and 2) family history of gestational hypertension. NEFA levels early in pregnancy were independently associated with sPTB, particularly before 34 weeks. We also detected a novel risk pattern suggesting that NEFAs together with HDL cholesterol may be related to sPTB.

摘要

我们认为,妊娠早期非酯化(游离)脂肪酸(NEFA)的蓄积会使女性面临自然早产(sPTB)的额外风险,并研究了NEFA、脂质和其他标志物之间的相互作用,以探索sPTB的发病途径。在一项嵌套于“妊娠暴露与子痫前期预防研究”(宾夕法尼亚州匹兹堡,1997 - 2001年)的病例对照研究中,我们测定了115例sPTB(<37周)女性和222例分娩发生在≥37周的女性在平均妊娠周数为9.4(范围4 - 20周)时采集的非空腹血清中的NEFA水平。还测量了C反应蛋白、总胆固醇、低密度脂蛋白和高密度脂蛋白(HDL)胆固醇、甘油三酯和尿酸。采用多分类逻辑回归模型评估NEFA水平三分位数与<34周和34 - 36周时sPTB的关系;采用因子分析来描述生物标志物模式。在调整协变量后,NEFA水平处于最高三分位数的女性与最低三分位数的女性相比,发生sPTB的可能性高2.02倍(95%置信区间:1.13,3.48)。在NEFA水平高的女性中,34周前发生sPTB的风险特别高(优势比 = 3.73,95%置信区间:1.33,10.44)。确定了六种生物标志物模式,其中两种与sPTB相关:1)NEFA和HDL胆固醇水平升高,2)妊娠期高血压家族史。妊娠早期的NEFA水平与sPTB独立相关,尤其是在34周前。我们还检测到一种新的风险模式,表明NEFA与HDL胆固醇可能与sPTB有关。

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