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February 13, 2021
 
 

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The association between dietary fatty acid consumption and the risk of setting up preeclampsia: a matched case–control analyze | SPS-202 test Questions and Practice Questions

  • 1.

    San 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).

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  • 2.

    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).

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  • three.

    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).

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    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).

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    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).

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  • 6.

    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).

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    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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    Calder, P. C. functional roles of fatty acids and their outcomes on human fitness. JPEN J. Parenter. Enteral. Nutr. 39, 18s–32s. https://doi.org/10.1177/0148607115595980 (2015).

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  • 9.

    Bermudez, B. et al. Oleic acid in olive oil: from a metabolic framework towards a clinical perspective. Curr. Pharm. Des. 17, 831–843. https://doi.org/10.2174/138161211795428957 (2011).

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  • 10.

    Pérez-Martínez, P., García-Ríos, A., Delgado-Lista, J., Pérez-Jiménez, F. & López-Miranda, J. Mediterranean diet prosperous in olive oil and obesity, metabolic syndrome and diabetes mellitus. Curr. Pharm. Des. 17, 769–777. https://doi.org/10.2174/138161211795428948 (2011).

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  • 11.

    Bakouei, F., Delavar, M. A., Mashayekh-Amiri, S., Esmailzadeh, S. & Taheri, Z. Efficacy of n-three fatty acids supplementation on the prevention of being pregnant brought about-hypertension or preeclampsia: a scientific evaluation and meta-evaluation, Taiwan. J. Obstet. Gynecol. 59, 8–15. https://doi.org/10.1016/j.tjog.2019.eleven.002 (2020).

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  • 12.

    Mackay, V. A. et al. Preeclampsia is linked to compromised maternal synthesis of long-chain polyunsaturated fatty acids, resulting in offspring deficiency. Hypertension 60, 1078–1085. https://doi.org/10.1161/hypertensionaha.112.197897 (2012).

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  • 13.

    Velzing-Aarts, F. V., van der Klis, F. R., van der Dijs, F. P. & Muskiet, F. A. Umbilical vessels of preeclamptic women have low contents of each n-three and n-6 long-chain polyunsaturated fatty acids. Am. J. Clin. Nutr. 69, 293–298. https://doi.org/10.1093/ajcn/sixty nine.2.293 (1999).

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  • 14.

    Mahomed, ok., Williams, M. A., King, I. B., Mudzamiri, S. & Woelk, G. B. Erythrocyte omega-three, omega-6 and trans fatty acids on the subject of possibility of preeclampsia among ladies supplying at Harare Maternity hospital, Zimbabwe. Physiol. Res. 56, 37–50 (2007).

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  • 15.

    Arvizu, M. et al. fats intake all through pregnancy and chance of preeclampsia: a prospective cohort analyze in Denmark. Eur. J. Clin. Nutr. 73, 1040–1048. https://doi.org/10.1038/s41430-018-0290-z (2019).

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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).

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  • 17.

    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).

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    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).

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  • 19.

    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).

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  • 20.

    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).

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  • 21.

    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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    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).

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