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富含特殊促解决介质(SPMs)的海洋油补充剂的促炎症消退作用及其在新冠后综合征(PCS)患者中的意义。

Pro-Resolving Inflammatory Effects of a Marine Oil Enriched in Specialized Pro-Resolving Mediators (SPMs) Supplement and Its Implication in Patients with Post-COVID Syndrome (PCS).

作者信息

Gracia Aznar Asun, Moreno Egea Fernando, Gracia Banzo Rafael, Gutierrez Rocio, Rizo Jose Miguel, Rodriguez-Ledo Pilar, Nerin Isabel, Regidor Pedro-Antonio

机构信息

Sociedad Española de Médicos Generales y de Familia (SEMG), 28005 Madrid, Spain.

Solutex GC SL, Avenida de la Transición Espanola 24, 28108 Alcobendas, Spain.

出版信息

Biomedicines. 2024 Sep 29;12(10):2221. doi: 10.3390/biomedicines12102221.

DOI:10.3390/biomedicines12102221
PMID:39457534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11505212/
Abstract

OBJECTIVES

This study aimed to evaluate the eicosanoid and pro-resolutive parameters in patients with Post-COVID Syndrome (PCS) during a 12-week supplementation with a marine oil enriched in specialized pro-resolving mediators (SPMs).

PATIENT AND METHODS

This study was conducted on 53 adult patients with PCS. The subjects included must have had a positive COVID-19 test (PCR, fast antigen test, or serologic test) and persistent symptoms related to COVID-19 at least 12 weeks before their enrolment in the study. The following parameters were evaluated: polyunsaturated fatty acids EPA, DHA, ARA, and DPA; specialized pro-resolving mediators (SPMs), 17-HDHA, 18-HEPE, 14-HDHA, resolvins, maresins, protectins, and lipoxins. The eicosanoids group included prostaglandins, thromboxanes, and leukotrienes. The development of the clinical symptoms of fatigue and dyspnea were evaluated using the Fatigue Severity Scale (FSS) and the Modified Medical Research Council (mMRC) Dyspnea Scale. Three groups with different intake amounts were evaluated (daily use of 500 mg, 1500 mg, and 3000 mg) and compared to a control group not using the product.

RESULTS

In the serum from patients with PCS, an increase in 17-HDHA, 18-HEPE, and 14-HDHA could be observed, and a decrease in the ratio between the pro-inflammatory and pro-resolutive lipid mediators was detected; both differences were significant ( < 0.05). There were no differences found between the three treatment groups. Fatigue and dyspnea showed a trend of improvement after supplementation in all groups.

CONCLUSIONS

A clear enrichment in the serum of the three monohydroxylated SPMs could be observed at a dosage of 500 mg per day. Similarly, a clear improvement in fatigue and dyspnea was observed with this dosage.

摘要

目的

本研究旨在评估新冠后综合征(PCS)患者在补充富含特殊促消退介质(SPMs)的鱼油12周期间的类二十烷酸和促消退参数。

患者与方法

本研究对53例成年PCS患者进行。纳入的受试者必须在参加本研究前至少12周新冠病毒检测(PCR、快速抗原检测或血清学检测)呈阳性且有与新冠相关的持续症状。评估了以下参数:多不饱和脂肪酸二十碳五烯酸(EPA)、二十二碳六烯酸(DHA)、花生四烯酸(ARA)和二十二碳五烯酸(DPA);特殊促消退介质(SPMs),17-羟二十二碳六烯酸(17-HDHA)、18-羟二十碳五烯酸(18-HEPE)、14-羟二十二碳六烯酸(14-HDHA)、消退素、maresin、保护素和脂氧素。类二十烷酸组包括前列腺素、血栓素和白三烯。使用疲劳严重程度量表(FSS)和改良医学研究委员会(mMRC)呼吸困难量表评估疲劳和呼吸困难的临床症状发展。评估了三组不同摄入量(每日使用500毫克、1500毫克和3000毫克)的情况,并与未使用该产品的对照组进行比较。

结果

在PCS患者的血清中,可观察到17-HDHA、18-HEPE和14-HDHA增加,且促炎和促消退脂质介质之间的比例降低;两者差异均有统计学意义(P<0.05)。三个治疗组之间未发现差异。所有组在补充后疲劳和呼吸困难均呈改善趋势。

结论

每天500毫克的剂量可使血清中三种单羟基化SPMs明显富集。同样,该剂量下疲劳和呼吸困难也有明显改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/93e27cd82c3e/biomedicines-12-02221-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/f622a6939935/biomedicines-12-02221-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/c44881c94565/biomedicines-12-02221-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/af10c758acbb/biomedicines-12-02221-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/f78e6243619a/biomedicines-12-02221-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/933743c9f498/biomedicines-12-02221-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/120834ee5040/biomedicines-12-02221-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/93e27cd82c3e/biomedicines-12-02221-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/f622a6939935/biomedicines-12-02221-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/19fa1c15970f/biomedicines-12-02221-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/c44881c94565/biomedicines-12-02221-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/af10c758acbb/biomedicines-12-02221-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/f78e6243619a/biomedicines-12-02221-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/933743c9f498/biomedicines-12-02221-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/120834ee5040/biomedicines-12-02221-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e940/11505212/93e27cd82c3e/biomedicines-12-02221-g008.jpg

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