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Inflammatory and oxidative stress markers associated with decreased cervical length in pregnancy

dc.contributor.authorVenkatesh, Kartik K.
dc.contributor.authorCantonwine, David E.
dc.contributor.authorFerguson, Kelly
dc.contributor.authorArjona, Melanie
dc.contributor.authorMeeker, John D.
dc.contributor.authorMcElrath, Thomas F.
dc.date.accessioned2016-10-17T21:20:24Z
dc.date.available2018-01-08T19:47:52Zen
dc.date.issued2016-11
dc.identifier.citationVenkatesh, Kartik K.; Cantonwine, David E.; Ferguson, Kelly; Arjona, Melanie; Meeker, John D.; McElrath, Thomas F. (2016). "Inflammatory and oxidative stress markers associated with decreased cervical length in pregnancy." American Journal of Reproductive Immunology 76(5): 376-382.
dc.identifier.issn1046-7408
dc.identifier.issn1600-0897
dc.identifier.urihttps://hdl.handle.net/2027.42/134275
dc.publisherWiley Periodicals, Inc.
dc.subject.otherpregnancy
dc.subject.othercervical length
dc.subject.othercervix
dc.subject.otherinflammation
dc.subject.otheroxidative stress
dc.titleInflammatory and oxidative stress markers associated with decreased cervical length in pregnancy
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelMicrobiology and Immunology
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/134275/1/aji12545_am.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/134275/2/aji12545.pdf
dc.identifier.doi10.1111/aji.12545
dc.identifier.sourceAmerican Journal of Reproductive Immunology
dc.identifier.citedreferenceSeong W, Lee DY, Koo TB. Do the levels of tumor makers or proinflammatory cytokines in mid‐trimester cervical fluid predict early‐stage cervical shortening? J Obstet Gynaecol Res. 2015; 41: 1715 – 1720.
dc.identifier.citedreferenceWu L, Chiou CC, Chang PY, Wu JT. Urinary 8‐OHdG: a marker of oxidative stress to DNA and a risk factor for cancer, atherosclerosis and diabetics. Clin Chim Acta. 2004; 339: 1 – 9.
dc.identifier.citedreferenceFerguson K, McElrath TF, Chen YH, Mukherjee B, Meeker JD. Longitudinal profiling of inflammatory cytokines and C‐reactive protein during uncomplicated and preterm pregnancy. Am J Reprod Immunol. 2014; 72: 326 – 336.
dc.identifier.citedreferenceBastek J, Hirshberg A, Chandrasekaran S, et al. Biomarkers and cervical length to predict spontaneous preterm birth in asymptomatic high‐risk women. Obstet Gynecol. 2013; 122: 283 – 289.
dc.identifier.citedreferenceMoroz L, Simhan HN. Rate of sonographic cervical shortening and biologic pathways of spontaneous preterm birth. Am J Obstet Gynecol. 2014; 210: e1 – e5.
dc.identifier.citedreferenceFerguson K, McElrath TF, Meeker JD. Environmental phthalate exposure and preterm birth. JAMA Pediatr. 2014; 168: 61 – 67.
dc.identifier.citedreferenceFerguson K, McElrath TF, Chen YH, Mukherjee B, Meeker JD. Urinary phthalate metabolites and biomarkers of oxidative stress in pregnant women: a repeated measures analysis. Environ Health Perspect. 2015; 123: 210 – 216.
dc.identifier.citedreferenceJiang Y, Scott AJ, Wild CJ. Secondary analysis of case‐control data. Stat Med. 2006; 25: 1323 – 1339.
dc.identifier.citedreferenceIams J, Goldenberg RL, Meis PJ, et al. The length of the cervix and the risk of spontaneous premature delivery. National Institute of Child Health and Human Development Maternal Fetal Medicine Unit Network. N Engl J Med. 1996; 334: 567 – 572.
dc.identifier.citedreferenceLarma J, Iams IA. Is sonographic assessment of the cervix necessary and helpful? Clin Obstet Gynecol. 2012; 55: 324 – 335.
dc.identifier.citedreferenceMeeker J, Hu H, Cantonwine DE, et al. Urinary phthalate metabolites in relation to preterm birth in Mexico city. Environ Health Perspect. 2009; 117: 1587 – 1592.
dc.identifier.citedreferenceCurry A, Vogel I, Skogstrand K, et al. Maternal plasma cytokines in early‐ and mid‐gestation of normal human pregnancy and their association with maternal factors. J Immunol. 2008; 77: 152 – 160.
dc.identifier.citedreferenceHolmes V, Wallace JM, Gilmore WS, McFaul P, Alexander HD. Plasma levels of the immunomodulatory cytokine interleukin‐10 during normal human pregnancy: a longitudinal study. Cytokine. 2003; 21: 265 – 269.
dc.identifier.citedreferenceWord R, Li XH, Hnat M, Carrick K. Dynamics of cervical remodeling during pregnancy and parturition: mechanisms and current concepts. Semin Reprod Med. 2007; 25: 69 – 79.
dc.identifier.citedreferenceRuiz R, Jallo N, Murphey C, Marti CN, Godbold E, Pickler RH. Second trimester maternal plasma levels of cytokines IL‐1Ra, Il‐6 and IL‐10 and preterm birth. J Perinatol. 2012; 32: 483 – 490.
dc.identifier.citedreferenceHarper M, Li L, Zhao Y, et al.; Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal‐Fetal Medicine Units Network. Change in mononuclear leukocyte responsiveness in midpregnancy and subsequent preterm birth. Obstet Gynecol. 2013; 121: 805 – 811.
dc.identifier.citedreferenceScholl T, Stein TP. Oxidant damage to DNA and pregnancy outcome. J Matern Fetal Neonatal Med. 2001; 10: 182 – 185.
dc.identifier.citedreferenceHung T, Lo LM, Chiu TH, et al. A longitudinal study of oxidative stress and antioxidant status in women with uncomplicated pregnancies throughout gestation. Reprod Sci. 2012; 17: 401 – 409.
dc.identifier.citedreferenceHsieh T, Chen SF, Lo LM, Li MJ, Yeh YL, Hung TH. The association between maternal oxidative stress at mid‐gestation and subsequent pregnancy complications. Reprod Sci. 2012; 19: 505 – 512.
dc.identifier.citedreferencePeter Stein T, Scholl TO, Schluter MD, et al. Oxidative stress early in pregnancy and pregnancy outcome. Free Radical Res. 2008; 42: 841 – 848.
dc.identifier.citedreferencePathak R, Suke SG, Ahmed T, et al. Organochlorine pesticide residue levels and oxidative stress in preterm delivery cases. Hum Exp Toxicol. 2010; 29: 351 – 358.
dc.identifier.citedreferenceFriedman A, Srinivas SK, Parry S, Elovitz MA, Wang E, Schwartz N. Can transabdominal ultrasound be used as a screening test for short cervical length? Am J Obstet Gynecol. 2013; 208: e1 – e7.
dc.identifier.citedreferenceSaul L, Kurtzman JT, Hagemann C, Ghamsary M, Wing DA. Is transabdominal sonography of the cervix after voiding a reliable method of cervical length assessment? J Ultrasound Med. 2008; 27: 1305 – 1311.
dc.identifier.citedreferenceIams J, Romero R, Culhane JF, Goldenberg RL. Primary, secondary, and tertiary interventions to reduce the morbidity and mortality of preterm birth. Lancet. 2008; 371: 164 – 175.
dc.identifier.citedreferenceGoldenberg R, Culhane JF, Iams JD, Romero R. Epidemiology and causes of preterm birth. Lancet. 2008; 371: 75 – 84.
dc.identifier.citedreferenceMoroz L, Simhan HN. Rate of sonographic cervical shortening and the risk of spontaneous preterm birth. Am J Obstet Gynecol. 2012; 206: e1 – e5.
dc.identifier.citedreferenceWei S, Fraser W, Luo ZC. Inflammatory cytokines and spontaneous preterm birth in asymptomatic women: a systematic review. Obstet Gynecol. 2010; 116: 393 – 401.
dc.identifier.citedreferenceGoldenberg R, Hauth JC, Andrews WW. Intrauterine infection and preterm delivery. N Engl J Med. 2000; 342: 1500 – 1507.
dc.identifier.citedreferenceConde‐Agudelo A, Papageorghiou AT, Kennedy SH, Villar J. Novel biomarkers for the prediction of the spontaneous preterm birth phenotype: a systematic review and meta‐analysis. BJOG. 2011; 118: 1042 – 1054.
dc.identifier.citedreferenceChallis J, Lockwood CJ, Myatt L, Norman JE, Strauss JF 3rd, Petraglia F. Inflammation and pregnancy. Reprod Sci. 2009; 16: 206 – 215.
dc.identifier.citedreferenceKalan A, Simhan HN. Mid‐trimester cervical inflammatory milieu and sonographic cervical length. Am J Obstet Gynecol. 2010; 203: e1 – e5.
dc.identifier.citedreferenceChandiramani M, Seed PT, Orsi NM, et al. Limited relationship between cervico‐vaginal fluid cytokine profiles and cervical shortening in women at high risk of spontaneous preterm birth. PLoS One. 2012; 7: e52412.
dc.identifier.citedreferenceBastek J, Elovitz MA. The role and challenges of biomarkers in spontaneous preterm birth and preeclampsia. Fertil Steril. 2013; 99: 1117 – 1123.
dc.identifier.citedreferenceBrou L, Almli LM, Pearce BD, et al. Dysregulated biomarkers induce distinct pathways in preterm birth. BJOG. 2012; 119: 458 – 473.
dc.identifier.citedreferenceRomero R, Espinoza J, Gonçalves LF, Kusanovic JP, Friel L, Hassan S. The role of inflammation and infection in preterm birth. Semin Reprod Med. 2007; 25: 21 – 39.
dc.identifier.citedreferenceHanna N, Hanna I, Hleb M, et al. Gestational age‐dependent expression of IL‐10 and its receptor in human placental tissues and isolated cytotrophoblasts. J Immunol. 2000; 164: 5721 – 5728.
dc.identifier.citedreferenceFerguson K, McElrath TF, Chen YH, Loch‐Caruso R, Mukherjee B, Meeker JD. Repeated measures of urinary oxidative stress biomarkers during pregnancy and preterm birth. Am J Obstet Gynecol. 2015; 212: e1 – e8.
dc.identifier.citedreferenceRoberts L, Morrow JD. Measurement of F(2)‐isoprostanes as an index of oxidative stress in vivo. Free Radic Biol Med. 2000; 28: 505 – 513.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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