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1 2.5 for gestational hypertension and 2.4 for preeclampsia).
2 ular risk factors in women with a history of preeclampsia.
3 f DLX5 might help explain certain aspects of preeclampsia.
4 printed status and no prior association with preeclampsia.
5 g disturbed imprinting, gene expression, and preeclampsia.
6 during pregnancy reduces the risk of preterm preeclampsia.
7 ples from healthy controls and patients with preeclampsia.
8 nary soluble nephrin levels (nephrinuria) in preeclampsia.
9 00 cohort, 5.6% (n = 23) were diagnosed with preeclampsia.
10 Maternal asthma increased the risk of preeclampsia.
11 n (sFlt-1) is implicated in the pathology of preeclampsia.
12 cluding 745 women with GH and 815 women with preeclampsia.
13 tein, precede clinical signs and symptoms of preeclampsia.
14 were the most consistent findings in GH and preeclampsia.
15 ed with severe gestational diseases, such as preeclampsia.
16 he preclinical and clinical phases of GH and preeclampsia.
17 l outcomes in women with PPCM complicated by preeclampsia.
18 elieved to mediate the signs and symptoms of preeclampsia.
19 egnancy (10-18 weeks), on the development of preeclampsia.
20 epidemiological association between PFOA and preeclampsia.
21 tabolite concentrations during gestation and preeclampsia.
22 to 18 weeks in 47 participants who developed preeclampsia.
23 he development of chronic hypertension after preeclampsia.
24 ir reported epidemiological association with preeclampsia.
25 with low serum vitamin D levels who develop preeclampsia.
26 lar weight 16 kDa) have been associated with preeclampsia.
27 ation in placental macrophages is present in preeclampsia.
28 licated by gestational hypertension (GH) and preeclampsia.
29 une response in women who went on to develop preeclampsia.
30 ts and harms of treatment of screen-detected preeclampsia.
31 egnancy were associated with a lower risk of preeclampsia.
32 amin D supplementation for the prevention of preeclampsia.
33 nificantly associated with increased risk of preeclampsia.
34 n pregnancy was proposed as a risk factor of preeclampsia.
35 available for 816, with 67 (8.2%) developing preeclampsia.
36 d evidence associating APOL1 expression with preeclampsia.
37 hage-trophoblast interaction, is involved in preeclampsia.
38 to predict biological processes affected in preeclampsia.
39 to study the association of the variant with preeclampsia.
40 olites measured during pregnancy and risk of preeclampsia.
41 d obesity, two conditions that predispose to preeclampsia.
42 ly altered in the umbilical veins of GDM and preeclampsia.
43 verse maternal and fetal outcomes, including preeclampsia.
44 3.7% (n = 62,728) were born to mothers with preeclampsia.
45 smoking, gestational diabetes mellitus, and preeclampsia.
46 al infarction, stroke, cerebral malaria, and preeclampsia.
47 half met blood pressure criteria for severe preeclampsia.
48 evalence in those exposed and not exposed to preeclampsia.
49 iated with a slight reduction in the risk of preeclampsia.
50 pregnancy-related medical condition such as preeclampsia.
51 profile similar to those found in women with preeclampsia.
52 history of spontaneous abortion and risk of preeclampsia.
53 roup of women with subclinical or unresolved preeclampsia.
54 tal diagnosis of gestational hypertension or preeclampsia.
55 onships between maternal genotype and severe preeclampsia.
56 turity, because prematurity is an outcome of preeclampsia.
57 organs, contributing to the pathogenesis of preeclampsia.
58 whether disturbed imprinting contributes to preeclampsia.
59 Seventeen of 39 women (44%) with PPCM had preeclampsia.
60 atients with PPCM that is not complicated by preeclampsia.
61 idence, that imprinted genes are involved in preeclampsia.
62 rce (USPSTF) recommendation on screening for preeclampsia.
63 ular disease, stroke, and stroke death after preeclampsia.
64 million women including >258 000 women with preeclampsia.
65 tension and the pregnancy related condition, preeclampsia.
66 sproportionally affected by risk factors for preeclampsia.
67 ophysiology and clinical unpredictability of preeclampsia.
68 vailable in 10 survivors with and 16 without preeclampsia.
69 in some congenital heart defects and preterm preeclampsia.
70 ibutable risk of gestational hypertension or preeclampsia (11% versus 5% incidence in one study).
71 women (20-38 years of age) with very preterm preeclampsia (23-32 weeks of gestation, systolic BP >/=1
72 men also have case fatality rates related to preeclampsia 3 times higher than rates among white women
73 9 to 9.2], P<0.001), as was the incidence of preeclampsia (3.0% vs. 11.3%; odds ratio, 0.24; 95% conf
74 control (N = 408) groups in the incidence of preeclampsia (8.08% vs. 8.33%, respectively; relative ri
76 val, 11%-59%) in 3 women were complicated by preeclampsia, a frequency greater than US population est
77 ine and serum samples for early diagnosis of preeclampsia, a life-threatening hypertensive disorder t
78 centa actively produces transthyretin and in preeclampsia, a significant amount is extruded into the
79 L, mean +/- SD, p > 0.05, n = 8), however in preeclampsia, a significant proportion is vesicle-associ
80 nt, r-AKI associated with increased risk for preeclampsia (adjusted odds ratio [aOR], 5.9; 95% confid
81 e increase in DD risk associated with severe preeclampsia (adjusted odds ratio, 5.49; 95% CI, 2.06-14
82 d risk for other adverse outcomes, including preeclampsia (adjusted OR, 1.59 [95% CI, 1.54-1.63]), pr
84 ; confidence interval, 1.3-13.1); late-onset preeclampsia (after week 34, hazard ratio, 2.0; confiden
85 IA) has been associated with a lower risk of preeclampsia among nulliparous women, but it remains unc
86 ate adjustment were applied to relate ROP to preeclampsia among the full cohort and in a subcohort of
87 1 and proteinuria in women with very preterm preeclampsia and appeared to prolong pregnancy without m
93 as emerged as a common finding in women with preeclampsia and likely is a causative factor in this di
94 but were only modestly associated with term preeclampsia and not associated with gestational hyperte
96 es affected by common complications, such as preeclampsia and preterm birth, display developmental ph
98 We found disturbed placental imprinting in preeclampsia and revealed potential candidates, includin
101 ibution of endocrine-disrupting chemicals to preeclampsia and suggest a modifiable means to reduce th
102 rictor sensitivity that is characteristic of preeclampsia and suggest that targeting sFLT1-induced pa
103 ify the evidence on the relationship between preeclampsia and the future risk of cardiovascular disea
104 o confirm association between imprinting and preeclampsia and to predict biological processes affecte
105 ith APS given pravastatin after the onset of preeclampsia and/or IUGR compared with women in the cont
107 /J x DBA/2 has been recognized as a model of preeclampsia, and complement activation has been implica
110 nation (c statistic >0.80) for prediction of preeclampsia, and positive predictive values of 4% in th
111 to placental insufficiency, hypertension, or preeclampsia; and small-for-gestational-age (SGA) neonat
112 e pregnancy and delivery outcomes, including preeclampsia (aRR 1.24; 95% CI, 1.07-1.43), infection (a
113 e as likely to have been exposed in utero to preeclampsia as controls with TD after adjustment for ma
116 (RGS2) in the mother has been implicated in preeclampsia as well as in the development of chronic hy
117 the incidence of gestational diabetes and of preeclampsia, as well as the incidence of adverse neonat
119 noncritical heart defects in offspring, and preeclampsia before 34 weeks was associated with critica
121 -onset preeclampsia, but are also markers of preeclampsia before clinical manifestation, and are asso
122 ng are most marked in severe and early-onset preeclampsia, but are also markers of preeclampsia befor
123 pregnant women before the clinical onset of preeclampsia, but its predictive value in women with sus
124 fferences in the associations between IA and preeclampsia by timing and method of IA were small, with
125 -gestation or preterm infant and early-onset preeclampsia (by week 34) significantly predicted premat
126 formed a nested case-control study of 12,650 preeclampsia cases and 50,600 matched control deliveries
128 ver, women with r-AKI had increased rates of preeclampsia compared with controls (23% versus 4%; P<0.
129 significantly higher in pregnant women with preeclampsia compared with normotensive pregnant women (
130 y activated (P <0.05) in pregnant women with preeclampsia compared with normotensive pregnant women.
131 entas of women with periodontitis-associated preeclampsia compared with that in normotensive pregnant
132 PAR-gamma was downregulated in patients with preeclampsia compared with that of healthy normotensive
133 cluded in-hospital arrhythmias, eclampsia or preeclampsia, congestive heart failure (CHF), length of
134 in 697 controls from the Finnish Genetics of Preeclampsia Consortium (FINNPEC) cohort to study the as
137 ctivation in trophoblast cells of women with preeclampsia corroborates the translational relevance of
138 ngest in offspring from pregnancies in which preeclampsia developed during late gestation and offspri
139 al heart defects in infants of women who had preeclampsia during pregnancy is poorly understood, desp
140 egnancy, and complications during pregnancy (preeclampsia, eclampsia, hemorrhage, and hyperemesis).
141 e studies included pregnant women with GH or preeclampsia, evaluating left ventricular structure and
142 d in peripheral blood of women who developed preeclampsia (FDR <0.05 in the Vitamin D Antenatal Asthm
143 lacental complications of pregnancy, such as preeclampsia, fetal growth restriction, and stillbirth.
144 elopment of pregnancy complications, such as preeclampsia, fetal growth restriction, and stillbirth.
145 ciated phenotype that encompassed eclampsia, preeclampsia, fetal/neonatal deaths, and small litter si
146 ncentrations and assess the association with preeclampsia from 1990 through 2006 for the C8 Health Pr
147 ing, prenatal glucocorticoid administration, preeclampsia, gestational age at delivery, days in inten
150 In time to event analysis, patients with preeclampsia had worse event-free survival during 1-year
152 nd three individuals were considered to have preeclampsia/HELLP syndrome before the definitive diagno
153 ternal body mass index, higher maternal age, preeclampsia, higher socioeconomic position (SEP) and ma
154 iomyopathy (PPCM), but it is unknown whether preeclampsia impacts clinical or left ventricular (LV) f
155 ther evaluation of statins for prevention of preeclampsia in a large-scale randomized clinical trial.
156 abortion is associated with a lower risk of preeclampsia in a later pregnancy, focusing on the hypot
158 owever, the polymorphism was associated with preeclampsia in a subgroup of overweight women (body mas
160 dels were used to calculate hazard ratios of preeclampsia in association with an interquartile range
162 en with hypertensive disorders of pregnancy, preeclampsia in particular, have an increased risk of ca
165 y were also strongly associated with preterm preeclampsia in subsequent pregnancies (early preterm pr
167 he occurrence of ROP was related to maternal preeclampsia in the full cohort and in a subcohort of P-
168 be predictive of the absence or presence of preeclampsia in the short term in women with singleton p
169 er had a negative predictive value (i.e., no preeclampsia in the subsequent week) of 99.3% (95% confi
170 be used to predict the short-term absence of preeclampsia in women in whom the syndrome is suspected
171 in D (25-hydroxyvitamin D [25OHD]) levels on preeclampsia incidence at trial entry and in the third t
172 d in weeks 10-18 of pregnancy did not reduce preeclampsia incidence in the intention-to-treat paradig
173 gnant women) and 25 were pregnant women with preeclampsia, including those with gestational hypertens
175 centa plays a central role in development of preeclampsia, investigation into the contribution of env
193 ading to intrauterine growth restriction and preeclampsia, is the failure of invading extravillous tr
194 ory of induced abortion have a lower risk of preeclampsia, it is difficult to evaluate whether the ob
195 ends in a birth protects against subsequent preeclampsia, it is unclear whether a pregnancy ending i
196 to the similarities in pathophysiology among preeclampsia, IUGR, and atherosclerotic cardiovascular d
198 ng congenital heart defects or early preterm preeclampsia, late preterm preeclampsia, term preeclamps
199 Many of the complications associated with preeclampsia lead to early induction of labor or cesarea
200 ptic serum is also aggregated and can induce preeclampsia-like symptoms in pregnant IL10(-/-) mice.
204 age, prepregnancy diabetes mellitus, preterm preeclampsia, multiple birth, and termination of pregnan
206 ce among women being evaluated for suspected preeclampsia (n = 1888) had wide-ranging test accuracy (
207 maturely to untreated women with and without preeclampsia (n=22 per group), no adverse effects of aph
208 years of follow-up among women with moderate preeclampsia, n = 102 cardiomyopathy events; 14.6/100,00
209 n-years of follow-up among women with severe preeclampsia, n = 27 cardiomyopathy events; 15.6/100,000
210 emopexin, which were decreased in women with preeclampsia, negatively correlated with proteinuria, ur
212 he increased aggregation of transthyretin in preeclampsia occurs at the post-transcriptional level an
215 ny vs no HDP, 1.54 (95% CI, 1.39-1.70) after preeclampsia or eclampsia, 1.51 (95% CI, 1.27-1.80) afte
216 ve disorder of pregnancy (severe or moderate preeclampsia or gestational hypertension) registered in
217 ampsia in a previous pregnancy, but not term preeclampsia or gestational hypertension, was associated
218 n and heparin, has not been shown to prevent preeclampsia or intrauterine growth restriction (IUGR).
220 l deaths (1 woman had used LMWH); 9 cases of preeclampsia or the hemolysis, elevated liver enzyme lev
221 me pregnancy and weakly associated with term preeclampsia (OR, 1.16; 95% CI, 1.06-1.27), but they wer
222 e interval [CI], 6.11-8.03) and late preterm preeclampsia (OR, 2.82; 95% CI, 2.38-3.34) in the same p
223 betes status, r-AKI remained associated with preeclampsia (OR, 4.7; 95% CI, 2.1 to 10.1) and adverse
224 were strongly associated with early preterm preeclampsia (OR, 7.00; 95% confidence interval [CI], 6.
225 gnancy (HDP) (gestational hypertension [GH], preeclampsia, or eclampsia) and 1.81 (95% CI, 1.44-2.27)
226 eclampsia: OR, 2.83; 95% CI, 2.11-3.79; term preeclampsia: OR, 0.98; 95% CI, 0.88-1.10; gestational h
227 a: OR, 2.37; 95% CI, 1.68-3.34; late preterm preeclampsia: OR, 2.04; 95% CI, 1.52-2.75) but were only
228 sia in subsequent pregnancies (early preterm preeclampsia: OR, 2.37; 95% CI, 1.68-3.34; late preterm
229 a: OR, 7.91; 95% CI, 6.06-10.3; late preterm preeclampsia: OR, 2.83; 95% CI, 2.11-3.79; term preeclam
230 defects in later pregnancies (early preterm preeclampsia: OR, 7.91; 95% CI, 6.06-10.3; late preterm
234 GS2 might be involved in the pathogenesis of preeclampsia particularly in overweight women and contri
238 sufficiency-associated complications such as preeclampsia (PE) and intrauterine growth restriction (I
244 t invasion and differentiation can result in preeclampsia (PE), a hypertensive disorder of pregnancy
247 During the pregnancy associated syndrome preeclampsia (PE), there is increased release of placent
249 supplementation had no effect on the risk of preeclampsia, reduced maternal serum vitamin D levels di
251 evidence that urinary EVs are reflective of preeclampsia-related altered podocyte protein expression
255 se aspirin in women at high risk for preterm preeclampsia resulted in a lower incidence of this diagn
256 F found adequate evidence that screening for preeclampsia results in a substantial benefit for the mo
259 ; 95% confidence interval [CI], 1.94-18.44), preeclampsia (RR, 2.43; 95% CI, 1.75-3.39), stillbirth (
260 tematically review the benefits and harms of preeclampsia screening and risk assessment for the US Pr
261 Evidence to estimate benefits and harms of preeclampsia screening and the test performance of diffe
263 udies directly compared the effectiveness of preeclampsia screening in a screened population vs an un
265 analysis using loci bearing unique GDM- and preeclampsia-specific loss-of-5hmC indicated its impact
268 or early preterm preeclampsia, late preterm preeclampsia, term preeclampsia, and gestational hyperte
270 otential benefits and harms of screening for preeclampsia, the effectiveness of risk prediction tools
271 curacy of screening and diagnostic tests for preeclampsia, the potential benefits and harms of screen
273 Currently, delivery is the only cure for preeclampsia; therefore, effective prevention and treatm
274 mpared with infants of women with late-onset preeclampsia, those with early onset (<34 weeks) had gre
275 or pregnancy-related complication, including preeclampsia, thrombotic microangiopathy, heart failure,
276 regnancies who were at high risk for preterm preeclampsia to receive aspirin, at a dose of 150 mg per
278 cid for rapid and routine diagnosis of early preeclampsia using electrochemical-surface enhanced Rama
284 for potential confounders demonstrated that preeclampsia was independently associated with an increa
288 in women with singleton pregnancies in whom preeclampsia was suspected (24 weeks 0 days to 36 weeks
291 owth factor, both biomarkers associated with preeclampsia, were measured on antepartum blood samples.
292 weeks gestation was associated with onset of preeclampsia, whereas significantly elevated hazard rati
294 Meta-analysis showed a higher risk of severe preeclampsia with coagulation factor V gene (proacceleri
295 ulty placentation manifests in the mother as preeclampsia with vascular damage, enhanced systemic inf
296 revalence is found among pregnant women with preeclampsia, with increased percentage of sites with BO
297 prior IA was associated with a lower risk of preeclampsia, with odds ratios of 0.9 (95% confidence in
298 low a derived cutoff) predict the absence of preeclampsia within 1 week after the first visit and whe
299 Flt-1:PlGF ratio above 38 for a diagnosis of preeclampsia within 4 weeks was 36.7% (95% CI, 28.4 to 4
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