患有不同过敏性疾病的孕妇的 N-3 多不饱和脂肪酸谱发生改变

Antonio Gázquez, Antonia M. Egea-Marín, Maya Sánchez-Martínez, Valentina Origüela, M. D. Molina-Ruano, L. García-Marcos, Elvira Larqué
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引用次数: 0

摘要

:近几十年来,过敏性疾病的发病率明显上升,约有 20% 的人受到影响,这已成为一个公共卫生问题。一些研究表明,哮喘和过敏症可能是膳食中 n-6 多元不饱和脂肪酸(PUFA)摄入量增加和 n-3 PUFA 摄入量减少的结果。在怀孕期间,胎儿依赖于从母体血液循环中经胎盘转移的 n-3 PUFA,这意味着母体血脂谱的改变可能会导致婴幼儿期过敏症的发生。本研究的目的是评估有过敏问题的孕妇体内的循环脂肪酸谱以及胎儿出生时血浆中的循环脂肪酸谱。在 NELA 队列(西班牙穆尔西亚)中收集了 73 名过敏孕妇和 179 名健康孕妇的血浆样本以及分娩时的脐带静脉血浆。孕妇过敏症是根据症状和皮肤点刺试验阳性来诊断的。脂肪酸图谱是通过气体色谱法测定的。与健康母亲相比,过敏母亲血浆中的 n-3 PUFA 百分比较低(过敏母亲:4.06 ± 0.15 vs. 对照组:4.66 ± 0.11,p = 0.002),尤其是患有哮喘或食物过敏的母亲。这导致过敏症(过敏症:9.45 ± 0.31 vs. 对照组:8.28 ± 0.20,p = 0.002)妇女的 n-6/n-3 PUFA 比率明显升高,主要是哮喘和食物过敏,这表明她们处于促炎症状态。在受特应性皮炎影响的妇女中也观察到同样的趋势(p = 0.094)。在脐带血中,尽管各组之间的 n-6/n-3 PUFA 比率没有差异,但与健康母亲所生的胎儿相比,过敏性母亲所生的胎儿的 n-3 PUFA 含量有降低的趋势(过敏性:5.63 ± 0.19 对对照组:6.17 ± 0.21,p = 0.093)。总之,过敏会导致孕妇在分娩时 n-3 PUFA 含量降低,n6-/n-3 脂肪酸比值升高,尤其是受哮喘和食物过敏影响的孕妇。在脐带血浆中也观察到了同样的趋势。患有过敏性疾病的妇女最好摄入更多的 n-3 PUFA,以改善她们的血脂状况、促炎状态及其后代的健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
N-3 Polyunsaturated Fatty Acid Profile Is Altered in Pregnant Women with Different Allergic Diseases
: The incidence of allergic problems has notably increased in recent decades, affecting approximately 20% of the population and becoming a public health issue. Some studies have suggested that asthma and atopy could result from an increased dietary intake of n-6 polyun-saturated fatty acids (PUFA) and a decreased intake of n-3 PUFA. During pregnancy, the fetus depends on the transplacental transfer of n-3 PUFA from maternal circulation, which implies that maternal lipid profile alterations might predispose to allergy onset during infancy and childhood. The aim of this study was to evaluate the circulating fatty acid profile in pregnant women with allergic problems as well as in fetal plasma at birth. Plasma samples from 73 allergic and 179 healthy pregnant women as well as cord venous plasma were collected at delivery in the NELA cohort (Murcia, Spain). Maternal allergy was diagnosed according to the symptoms and via a positive skin prick test. The fatty acid profile was determined by gas cromatography. The allergic mothers had a lower percentage of n-3 PUFA in the plasma compared to the healthy ones (Allergic: 4.06 ± 0.15 vs. Control: 4.66 ± 0.11, p = 0.002), especially in those with asthma or food allergies. This contributed to a significantly higher n-6/n-3 PUFA ratio in women with allergies (Allergic: 9.45 ± 0.31 vs. Control: 8.28 ± 0.20, p = 0.002), mainly asthma and food allergies, which was indicative of a proinflammatory status. The same tendency was observed in women affected by atopic dermatitis ( p = 0.094). In cord blood, despite the fact that there were no differences in the n-6/n-3 PUFA ratio between the groups, the fetuses born from allergic mothers showed a tendency towards lower n-3 PUFA content compared to those born from healthy mothers (Allergic: 5.63 ± 0.19 vs. Control: 6.17 ± 0.21, p = 0.093). In conclusion, allergy led to a decreased n-3 PUFA and an increased n6-/n-3 ratio fatty acid profile in pregnant women at delivery, especially in those affected by asthma and food allergies. The same tendency was observed in cord plasma. A higher n-3 PUFA consumption could be desirable in women with allergic diseases in order to improve their lipid profile and proinflammatory status and their offspring’s health.
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