linoleic-acid and Endometriosis

linoleic-acid has been researched along with Endometriosis* in 2 studies

Other Studies

2 other study(ies) available for linoleic-acid and Endometriosis

ArticleYear
Metabolomic Signature of Endometrial Cancer.
    Journal of proteome research, 2018, 02-02, Volume: 17, Issue:2

    Endometrial cancer (EC) is the most common cancer of the female reproductive tract in developed countries. At the moment, no effective screening system is available. Here, we evaluate the diagnostic performance of a serum metabolomic signature. Two enrollments were carried out, one consisting of 168 subjects: 88 with EC and 80 healthy women, was used for building the classification models. The second (used to establish the performance of the classification algorithm) was consisted of 120 subjects: 30 with EC, 30 with ovarian cancer, 10 with benign endometrial disease, and 50 healthy controls. Two ensemble models were built, one with all EC versus controls (Model I) and one in which EC patients were aggregated according to their histotype (Model II). Serum metabolomic analysis was conducted via gas chromatography-mass spectrometry, while classification was done by an ensemble learning machine. Accuracy ranged from 62% to 99% for the Model I and from 67% to 100% for the Model II. Ensemble model showed an accuracy of 100% both for Model I and II. The most important metabolites in class separation were lactic acid, progesterone, homocysteine, 3-hydroxybutyrate, linoleic acid, stearic acid, myristic acid, threonine, and valine. The serum metabolomics signature of endometrial cancer patients is peculiar because it differs from that of healthy controls and from that of benign endometrial disease and from other gynecological cancers (such as ovarian cancer).

    Topics: 3-Hydroxybutyric Acid; Aged; Biomarkers, Tumor; Case-Control Studies; Diagnosis, Differential; Endometrial Neoplasms; Endometriosis; Endometrium; Female; Gas Chromatography-Mass Spectrometry; Homocysteine; Humans; Lactic Acid; Linoleic Acid; Machine Learning; Metabolome; Metabolomics; Middle Aged; Myristic Acid; Progesterone; Prospective Studies; Stearic Acids; Threonine; Valine

2018
Oral eicosapentaenoic acid supplementation as possible therapy for endometriosis.
    Fertility and sterility, 2008, Volume: 90, Issue:4 Suppl

    To investigate the anti-inflammatory effect of n-3 eicosapentaenoic acid (EPA) compared with n-6 linoleic acid (LA) in an endometriosis rat model. We focused on the relationship between lipid metabolism and inflammatory reactions in endometriosis based on the hypothesis that a lipid intake imbalance is one of the factors responsible for the recent increase of endometriosis.. Prospective, randomized experimental study.. Animal surgery laboratory in a university hospital.. Sprague-Dawley rats (female, 6 weeks old).. Rats were fed a diet with EPA (n = 9) or with LA (n = 9) for 2 weeks. Two weeks after feeding, the uterus was autotransplanted to the peritoneum to construct an endometriosis model. Feeding was continued for a total of 6 weeks. Two and 4 weeks after autotransplantation, three rats of each group were killed and evaluated.. Endometriotic lesions were morphologically evaluated and their fatty acid composition was examined. Gene expression in these tissues was evaluated by cDNA microarray analysis and quantative real-time reverse transcriptase-polymerase chain reaction (RT-PCR).. In the EPA group, the n-3:n-6 ratio in each tissue significantly increased and the thickening of the interstitium, an active site for inflammation in endometriosis, was significantly suppressed (0.30 +/- 0.09 mm [EPA group] vs. 0.77 +/- 0.23 mm [LA group]). The mRNA of metalloproteinases, interleukin-1beta, interleukin-1r, prostaglandin E synthase (Ptges), and nuclear factor (NF)-kappaB were reduced in the EPA group.. EPA supplementation might be a valid strategy for the treatment of endometriosis.

    Topics: Administration, Oral; Animals; Dietary Supplements; Eicosapentaenoic Acid; Endometriosis; Female; Gene Expression; Humans; Linoleic Acid; Lipid Metabolism; Random Allocation; Rats; Rats, Sprague-Dawley

2008