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IBM SPSS study tipsThe association between dietary fatty acid consumption and the risk of setting up preeclampsia: a matched case–control analyze | SPS-202 test Questions and Practice QuestionsSan Juan-Reyes, S., Gómez-Oliván, L. M., Islas-Flores, H. & Dublán-García, O. Oxidative stress in being pregnant complicated by using preeclampsia. Arch. Biochem. Biophys. 681, 108255. https://doi.org/10.1016/j.abb.2020.108255 (2020). Hypertension in being pregnant. file of the American college of Obstetricians and Gynecologists’ task drive on hypertension in pregnancy. Obstet. Gynecol. 122, 1122–1131. https://doi.org/10.1097/01.Aog.0000437382.03963.88 (2013). Khan, okay. S., Wojdyla, D., Say, L., Gülmezoglu, A. M. & Van appear, P. F. WHO analysis of factors of maternal demise: a systematic evaluate. Lancet 367, 1066–1074. https://doi.org/10.1016/s0140-6736(06)68397-9 (2006). Abalos, E. et al. Pre-eclampsia, eclampsia and antagonistic maternal and perinatal effects: a secondary evaluation of the realm health firm Multicountry Survey on Maternal and newborn health. BJOG 121(Suppl 1), 14–24. https://doi.org/10.1111/1471-0528.12629 (2014). Hernández-Díaz, S., Toh, S. & Cnattingius, S. risk of pre-eclampsia in first and subsequent pregnancies: potential cohort examine. BMJ (Clin. Res. Ed.) 338, 2255. https://doi.org/10.1136/bmj.b2255 (2009). Mensink, R. P. & Katan, M. B. impact of dietary fatty acids on serum lipids and lipoproteins. A meta-analysis of 27 trials. Arterioscler. Thromb. 12, 911–919. https://doi.org/10.1161/01.atv.12.eight.911 (1992). Mensink, R. P., Zock, P. L., Kester, A. D. & Katan, M. B. outcomes of dietary fatty acids and carbohydrates on the ratio of serum complete to HDL cholesterol and on serum lipids and apolipoproteins: a meta-analysis of 60 controlled trials. Am. J. Clin. Nutr. seventy seven, 1146–1155. https://doi.org/10.1093/ajcn/77.5.1146 (2003). 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Yusuf, H., Subih, H. S., Obeidat, B. S. & Sharkas, G. Associations of macro and micronutrients and antioxidants intakes with preeclampsia: a case-handle examine in Jordanian pregnant women. Nutr. Metab. Cardiovasc. Dis. 29, 458–466. https://doi.org/10.1016/j.numecd.2019.01.008 (2019). Nandi, A., Wadhwani, N., Randhir, okay., Wagh, G. & Joshi, S. R. affiliation of diet D with fatty acids in being pregnant. Prostaglandins Leukot. Essent. Fatty Acids 157, 102030. https://doi.org/10.1016/j.plefa.2019.102030 (2020). Stark, okay. D., Van Elswyk, M. E., Higgins, M. R., Weatherford, C. A. & Salem, N. Jr. global survey of the omega-three fatty acids, docosahexaenoic acid and eicosapentaenoic acid in the blood flow of match adults. Prog. Lipid Res. 63, 132–152. https://doi.org/10.1016/j.plipres.2016.05.001 (2016). Nandi, A., Wadhwani, N., Randhir, okay., Wagh, G. & Joshi, S. R. association of vitamin D with fatty acids in being pregnant. Prostaglandins Leukot. Essent. Fatty Acids https://doi.org/10.1016/j.plefa.2019.102030 (2019). Wang, Y., Walsh, S. W. & Kay, H. H. Placental tissue ranges of nonesterified polyunsaturated fatty acids in usual and preeclamptic pregnancies. Hypertens. pregnancy 24, 235–245. https://doi.org/10.1080/10641950500281118 (2005). Qiu, C. et al. Erythrocyte omega-three and omega-6 polyunsaturated fatty acids and preeclampsia risk in Peruvian girls. Arch. Gynecol. Obstet. 274, 97–103. https://doi.org/10.1007/s00404-006-0140-4 (2006). Oken, E. et al. food regimen all the way through being pregnant and chance of preeclampsia or gestational hypertension. Ann. Epidemiol. 17, 663–668. https://doi.org/10.1016/j.annepidem.2007.03.003 (2007). Bakheit, k. H., Ghebremeskel, okay., Pol, k., Elbashir, M. I. & Adam, I. Erythrocyte omega-3 and omega-6 fatty acids profile in Sudanese women with pre-eclampsia. J. Obstet. Gynaecol. 30, 151–154. https://doi.org/10.3109/01443610903391005 (2010). Dangat, k. D. et al. lengthy-chain polyunsaturated fatty acid composition of breast milk in pre-eclamptic mothers. Neonatology 97, 190–194. https://doi.org/10.1159/000252971 (2010). Wadhwani, N. S. et al. decreased maternal erythrocyte long chain polyunsaturated fatty acids exist in early pregnancy in preeclampsia. Lipids 51, eighty five–94. https://doi.org/10.1007/s11745-015-4098-5 (2016). Jones, M. L., Mark, P. J., Mori, T. A., Keelan, J. A. & Waddell, B. J. Maternal dietary omega-three fatty acid supplementation reduces placental oxidative stress and raises fetal and placental boom within the rat. Biol. Reprod. 88, 37. https://doi.org/10.1095/biolreprod.112.103754 (2013). Burton, G. J. & Jauniaux, E. Oxidative stress. most appropriate Pract. Res. Clin. Obstet. Gynaecol. 25, 287–299. https://doi.org/10.1016/j.bpobgyn.2010.10.016 (2011). Aouache, R., Biquard, L., Vaiman, D. & Miralles, F. Oxidative stress in preeclampsia and placental illnesses. Int. J. Mol. Sci. https://doi.org/10.3390/ijms19051496 (2018). Roberts, J. M. & Escudero, C. The placenta in preeclampsia. being pregnant Hypertens. 2, 72–83. https://doi.org/10.1016/j.preghy.2012.01.001 (2012). Imhoff-Kunsch, B., Briggs, V., Goldenberg, T. & Ramakrishnan, U. impact of n-3 long-chain polyunsaturated fatty acid intake all the way through being pregnant on maternal, infant, and baby health effects: a scientific review. Paediatr. Perinat. Epidemiol. 26(Suppl 1), 91–107. https://doi.org/10.1111/j.1365-3016.2012.01292.x (2012). Larque, E., Gil-Sanchez, A., Prieto-Sanchez, M. T. & Koletzko, B. Omega 3 fatty acids, gestation and pregnancy consequences. Br. J. Nutr. 107(Suppl 2), S77-eighty four. https://doi.org/10.1017/s0007114512001481 (2012). Jones, M. L., Mark, P. J. & Waddell, B. J. Maternal omega-three fatty acid consumption raises placental labyrinthine antioxidant skill but doesn't offer protection to in opposition t fetal boom limit precipitated with the aid of placental ischaemia-reperfusion damage. replica 146, 539–547. https://doi.org/10.1530/rep-13-0282 (2013). Peng, J. et al. Maternal eicosapentaenoic acid feeding promotes placental angiogenesis through a Sirtuin-1 unbiased inflammatory pathway. Biochim. Biophys. Acta Mol. mobile Biol. Lipids 147–157, 2019. https://doi.org/10.1016/j.bbalip.2018.eleven.003 (1864). Sorensen, J. D. et al. outcomes of fish oil supplementation within the third trimester of being pregnant on prostacyclin and thromboxane construction. Am. J. Obstet. Gynecol. 168, 915–922. https://doi.org/10.1016/s0002-9378(12)90845-5 (1993). Zhou, C. C. et al. Angiotensin receptor agonistic autoantibodies result in pre-eclampsia in pregnant mice. Nat. Med. 14, 855–862. https://doi.org/10.1038/nm.1856 (2008). Siddiqui, A. H. et al. Angiotensin receptor agonistic autoantibody is highly regular in preeclampsia: correlation with sickness severity. Hypertension 55, 386–393. https://doi.org/10.1161/hypertensionaha.109.140061 (2010). Xia, Y., Zhou, C. C., Ramin, S. M. & Kellems, R. E. Angiotensin receptors, autoimmunity, and preeclampsia. J. Immunol. 179, 3391–3395. https://doi.org/10.4049/jimmunol.179.6.3391 (2007). Zhang, Q. et al. Cadmium-brought about immune abnormality is a key pathogenic event in human and rat fashions of preeclampsia. Environ. Pollut. 218, 770–782. https://doi.org/10.1016/j.envpol.2016.07.073 (2016). Wallukat, G. et al. patients with preeclampsia enhance agonistic autoantibodies towards the angiotensin AT1 receptor. J. Clin. Investig. 103, 945–952. https://doi.org/10.1172/jci4106 (1999). Xia, Y., Ramin, S. M. & Kellems, R. E. talents roles of angiotensin receptor-activating autoantibody in the pathophysiology of preeclampsia. Hypertension 50, 269–275. https://doi.org/10.1161/hypertensionaha.107.091322 (2007). Zhang, Q. et al. Progesterone attenuates hypertension and autoantibody levels to the angiotensin II class 1 receptor in accordance with increased cadmium throughout being pregnant. Placenta 62, 16–24. https://doi.org/10.1016/j.placenta.2017.12.004 (2018). Liu, H. et al. Lipoxin A4 suppresses angiotensin II classification 1 receptor autoantibody in preeclampsia via modulating caspase-1. phone demise Dis. 11, seventy eight. https://doi.org/10.1038/s41419-020-2281-y (2020). Cao, Y. et al. Adherence to a Dietary procedures to stop Hypertension (sprint)-trend weight loss plan relating to preeclampsia: a case-handle study. Sci. Rep. 10, 9078. https://doi.org/10.1038/s41598-020-65912-2 (2020). Hypertensive disorders in being pregnant Subgroup chinese Society of Obstetrics and Gynecology. diagnosis and remedy guideline of hypertensive disorders in being pregnant. Chin. J. Obstet. Gynecol. 50, 721–728. https://doi.org/10.3760/cma.j.issn.0529-567x.2015.10.001 (2015). Zhang, C. X. & Ho, S. C. Validity and reproducibility of a meals frequency Questionnaire amongst chinese language girls in Guangdong province. Asia Pac. J. Clin. Nutr. 18, 240–250 (2009). Yang, Y. chinese language meals Composition desk 2004 75–247 (Peking school scientific Press, Beijing, 2005). El-Serag, H. B., Satia, J. A. & Rabeneck, L. Dietary consumption and the chance of gastro-oesophageal reflux disease: a go sectional look at in volunteers. intestine 54, eleven–17. https://doi.org/10.1136/gut.2004.040337 (2005). Zhu, Y. H. et al. Dietary intake of fatty acids, complete cholesterol, and stomach melanoma in a chinese language population. nutrients https://doi.org/10.3390/nu11081730 (2019). Willett, W. C., Howe, G. R. & Kushi, L. H. Adjustment for total energy consumption in epidemiologic reports. 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