Role of Circulating Cell-free DNA Levels in Patients With Severe Preeclampsia and HELLP Syndrome

BACKGROUND Increased plasma levels of circulating cell-free DNA (c-f DNA) have been recently described in diseases related to ischemia and/or hypoxia. Preeclampsia (PCL) is a hypertensive disorder of pregnancy, of unknown origin, where a defective placentation resulting in placental ischemia plays a...

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Veröffentlicht in:American journal of hypertension 2013-12, Vol.26 (12), p.1377-1380
Hauptverfasser: Miranda, Maria L., Macher, Hada C., Muñoz-Hernández, Rocio, Vallejo-Vaz, Antonio, Moreno-Luna, Rafael, Villar, Jose, Guerrero, Juan M., Stiefel, Pablo
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container_end_page 1380
container_issue 12
container_start_page 1377
container_title American journal of hypertension
container_volume 26
creator Miranda, Maria L.
Macher, Hada C.
Muñoz-Hernández, Rocio
Vallejo-Vaz, Antonio
Moreno-Luna, Rafael
Villar, Jose
Guerrero, Juan M.
Stiefel, Pablo
description BACKGROUND Increased plasma levels of circulating cell-free DNA (c-f DNA) have been recently described in diseases related to ischemia and/or hypoxia. Preeclampsia (PCL) is a hypertensive disorder of pregnancy, of unknown origin, where a defective placentation resulting in placental ischemia plays an important role. HELLP syndrome (haemolysis, elevated liver enzymes, and low platelet count) is the most serious form of PCL. The origin of the disease is unknown, and there are no markers to help us to make an early diagnosis of disease or to predict patients who are at risk of suffering serious complications. METHODS We measured circulating c-f DNA levels in a group of control pregnant women (n = 20), patients with mild PCL (n = 9), patients with severe PCL (n = 24), and patients with HELLP syndrome (n = 8). RESULTS Values of circulating c-f DNA were 333.59±64.3ng/ml in control subjects; 635.11±111.7ng/ml in patients with mild PCL; 1,264.63±127.1ng/ml in patients with severe PCL, and 1,595.95±269.8ng/ml in patients with HELPP syndrome. (P < 0.0001). Values of c-f DNA >950ng/ml had a sensitivity and specificity for detecting severe PCL and/or HELLLP syndrome of 0.71 and 0.93, respectively. CONCLUSIONS As far as we know, this is the first report of increased c-f DNA levels in HELLP syndrome. In this preliminary report, we have observed a gradual and strong relation between c-f DNA levels and range of severity of PCL, with it the highest in patients with HELLP syndrome. Further studies are needed for evaluating the utility of this technique in hypertensive disorders of pregnancy and, particularly, in HELLP syndrome.
doi_str_mv 10.1093/ajh/hpt187
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Preeclampsia (PCL) is a hypertensive disorder of pregnancy, of unknown origin, where a defective placentation resulting in placental ischemia plays an important role. HELLP syndrome (haemolysis, elevated liver enzymes, and low platelet count) is the most serious form of PCL. The origin of the disease is unknown, and there are no markers to help us to make an early diagnosis of disease or to predict patients who are at risk of suffering serious complications. METHODS We measured circulating c-f DNA levels in a group of control pregnant women (n = 20), patients with mild PCL (n = 9), patients with severe PCL (n = 24), and patients with HELLP syndrome (n = 8). RESULTS Values of circulating c-f DNA were 333.59±64.3ng/ml in control subjects; 635.11±111.7ng/ml in patients with mild PCL; 1,264.63±127.1ng/ml in patients with severe PCL, and 1,595.95±269.8ng/ml in patients with HELPP syndrome. (P &lt; 0.0001). Values of c-f DNA &gt;950ng/ml had a sensitivity and specificity for detecting severe PCL and/or HELLLP syndrome of 0.71 and 0.93, respectively. CONCLUSIONS As far as we know, this is the first report of increased c-f DNA levels in HELLP syndrome. In this preliminary report, we have observed a gradual and strong relation between c-f DNA levels and range of severity of PCL, with it the highest in patients with HELLP syndrome. Further studies are needed for evaluating the utility of this technique in hypertensive disorders of pregnancy and, particularly, in HELLP syndrome.</description><identifier>ISSN: 0895-7061</identifier><identifier>EISSN: 1941-7225</identifier><identifier>DOI: 10.1093/ajh/hpt187</identifier><identifier>PMID: 24103646</identifier><identifier>CODEN: AJHYE6</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adult ; Biomarkers - blood ; Case-Control Studies ; Cell-Free System - metabolism ; DNA - blood ; Female ; Follow-Up Studies ; HELLP Syndrome - blood ; HELLP Syndrome - diagnosis ; HELLP Syndrome - metabolism ; Hospitals, Maternity ; Humans ; Pre-Eclampsia - blood ; Pre-Eclampsia - diagnosis ; Pre-Eclampsia - metabolism ; Predictive Value of Tests ; Pregnancy ; Sensitivity and Specificity ; Severity of Illness Index</subject><ispartof>American journal of hypertension, 2013-12, Vol.26 (12), p.1377-1380</ispartof><rights>American Journal of Hypertension, Ltd 2013. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2013</rights><rights>American Journal of Hypertension, Ltd 2013. All rights reserved. For Permissions, please email: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-a5df642d3d62e92537c1a839c6876857c8eb6b4b6d461f9ad987fc17f72ab273</citedby><cites>FETCH-LOGICAL-c381t-a5df642d3d62e92537c1a839c6876857c8eb6b4b6d461f9ad987fc17f72ab273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24103646$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miranda, Maria L.</creatorcontrib><creatorcontrib>Macher, Hada C.</creatorcontrib><creatorcontrib>Muñoz-Hernández, Rocio</creatorcontrib><creatorcontrib>Vallejo-Vaz, Antonio</creatorcontrib><creatorcontrib>Moreno-Luna, Rafael</creatorcontrib><creatorcontrib>Villar, Jose</creatorcontrib><creatorcontrib>Guerrero, Juan M.</creatorcontrib><creatorcontrib>Stiefel, Pablo</creatorcontrib><title>Role of Circulating Cell-free DNA Levels in Patients With Severe Preeclampsia and HELLP Syndrome</title><title>American journal of hypertension</title><addtitle>AJHYPE</addtitle><addtitle>Am J Hypertens</addtitle><description>BACKGROUND Increased plasma levels of circulating cell-free DNA (c-f DNA) have been recently described in diseases related to ischemia and/or hypoxia. Preeclampsia (PCL) is a hypertensive disorder of pregnancy, of unknown origin, where a defective placentation resulting in placental ischemia plays an important role. HELLP syndrome (haemolysis, elevated liver enzymes, and low platelet count) is the most serious form of PCL. The origin of the disease is unknown, and there are no markers to help us to make an early diagnosis of disease or to predict patients who are at risk of suffering serious complications. METHODS We measured circulating c-f DNA levels in a group of control pregnant women (n = 20), patients with mild PCL (n = 9), patients with severe PCL (n = 24), and patients with HELLP syndrome (n = 8). RESULTS Values of circulating c-f DNA were 333.59±64.3ng/ml in control subjects; 635.11±111.7ng/ml in patients with mild PCL; 1,264.63±127.1ng/ml in patients with severe PCL, and 1,595.95±269.8ng/ml in patients with HELPP syndrome. (P &lt; 0.0001). Values of c-f DNA &gt;950ng/ml had a sensitivity and specificity for detecting severe PCL and/or HELLLP syndrome of 0.71 and 0.93, respectively. CONCLUSIONS As far as we know, this is the first report of increased c-f DNA levels in HELLP syndrome. In this preliminary report, we have observed a gradual and strong relation between c-f DNA levels and range of severity of PCL, with it the highest in patients with HELLP syndrome. 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Preeclampsia (PCL) is a hypertensive disorder of pregnancy, of unknown origin, where a defective placentation resulting in placental ischemia plays an important role. HELLP syndrome (haemolysis, elevated liver enzymes, and low platelet count) is the most serious form of PCL. The origin of the disease is unknown, and there are no markers to help us to make an early diagnosis of disease or to predict patients who are at risk of suffering serious complications. METHODS We measured circulating c-f DNA levels in a group of control pregnant women (n = 20), patients with mild PCL (n = 9), patients with severe PCL (n = 24), and patients with HELLP syndrome (n = 8). RESULTS Values of circulating c-f DNA were 333.59±64.3ng/ml in control subjects; 635.11±111.7ng/ml in patients with mild PCL; 1,264.63±127.1ng/ml in patients with severe PCL, and 1,595.95±269.8ng/ml in patients with HELPP syndrome. (P &lt; 0.0001). Values of c-f DNA &gt;950ng/ml had a sensitivity and specificity for detecting severe PCL and/or HELLLP syndrome of 0.71 and 0.93, respectively. CONCLUSIONS As far as we know, this is the first report of increased c-f DNA levels in HELLP syndrome. In this preliminary report, we have observed a gradual and strong relation between c-f DNA levels and range of severity of PCL, with it the highest in patients with HELLP syndrome. Further studies are needed for evaluating the utility of this technique in hypertensive disorders of pregnancy and, particularly, in HELLP syndrome.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>24103646</pmid><doi>10.1093/ajh/hpt187</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Biomarkers - blood
Case-Control Studies
Cell-Free System - metabolism
DNA - blood
Female
Follow-Up Studies
HELLP Syndrome - blood
HELLP Syndrome - diagnosis
HELLP Syndrome - metabolism
Hospitals, Maternity
Humans
Pre-Eclampsia - blood
Pre-Eclampsia - diagnosis
Pre-Eclampsia - metabolism
Predictive Value of Tests
Pregnancy
Sensitivity and Specificity
Severity of Illness Index
title Role of Circulating Cell-free DNA Levels in Patients With Severe Preeclampsia and HELLP Syndrome
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