Clinical characterization and outcomes of preeclampsia with normal angiogenic profile

被引:127
作者
Rana, Sarosh [1 ,2 ]
Schnettler, William T. [1 ,2 ]
Powe, Camille [3 ]
Wenger, Julia [4 ]
Salahuddin, Saira [1 ,2 ]
Cerdeira, Ana Sofia [2 ,5 ,6 ]
Verlohren, Stefan [7 ]
Perschel, Frank H. [8 ]
Arany, Zoltan [2 ,5 ]
Lim, Kee-Hak [9 ]
Thadhani, Ravi [4 ]
Karumanchi, S. Ananth [1 ,2 ,5 ,10 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Maternal Fetal Med, Dept Obstet & Gynecol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Harvard Univ, Sch Med, Dept Med, Brigham & Womens Hosp, Boston, MA USA
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Nephrol,Dept Med, Boston, MA USA
[5] Beth Israel Deaconess Med Ctr, Div Nephrol, Dept Med, Boston, MA 02215 USA
[6] Gulbenkian Programme Adv Med Educ, Lisbon, Portugal
[7] Charite, Dept Obstet, Campus Virchow Clin, D-13353 Berlin, Germany
[8] Charite, Dept Lab Med Clin Chem & Pathobiochem, D-13353 Berlin, Germany
[9] Boston Maternal Fetal Med, Boston, MA USA
[10] Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
Adverse outcomes; Angiogenic factors; Non-angiogenic preeclampsia; PLACENTAL GROWTH-FACTOR; MATERNAL PLASMA-CONCENTRATIONS; SOLUBLE ENDOGLIN; PREGNANCY; HYPERTENSION; DIAGNOSIS; KIDNEY; WOMEN; COMPLICATIONS; DISEASE;
D O I
10.3109/10641955.2013.784788
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To compare the clinical characteristics and outcomes of preeclamptic women presenting with a normal plasma angiogenic profile with those subjects who are characterized by an abnormal angiogenic profile. Methods: This was a secondary analysis of a prospective cohort study in women presenting to obstetrical triage at <37 weeks of gestation and diagnosed with preeclampsia within 2 weeks of enrollment and in whom angiogenic factors (sFlt1 and PlGF) measurements were available. Patients were divided into two groups based on their circulating levels of these factors described as a ratio; the sFlt1/PlGF ratio, non-angiogenic preeclampsia (sFlt1/PlGF ratio <85) and angiogenic preeclampsia (sFlt1/PlGF ratio >= 85). The data are presented by sFlt1/PlGF category using median and quartile 1-quartile 3 for continuous variables and by frequency and sample sizes for categorical variables. Results: In our cohort, the patients with non-angiogenic preeclampsia (N=46) were more obese [BMI: 35.2 (31.6, 38.7) versus 31.1 (28.0, 39.0), p = 0.04], more likely to have preexisting diabetes (21.7% versus 2.0%, p = 0.002) and presented at a later gestational age [35 (32, 37) versus 32 (29, 34) weeks, p<0.0001] as compared with women with angiogenic preeclampsia (N=51). Women with non-angiogenic preeclampsia had no serious adverse outcomes (elevated liver function tests/low platelets: 0% versus 23.5%, abruption: 0% versus 9.8%, pulmonary edema: 0% versus 3.9%, eclampsia: 0% versus 2.0 %, small for gestational age: 0% versus 17.7% and fetal/neonatal death: 0% versus 5.9%) as compared with women with angiogenic preeclampsia. The rate of preterm delivery <34 weeks was 8.7% in non-angiogenic preeclampsia compared with 64.7% in angiogenic preeclampsia (p<0.0001). Interestingly, delivery between 34 and 37 weeks and resource utilization (hospital admission days) were similar in the two groups. Conclusion: In contrast to the angiogenic form, the non-angiogenic form of preeclampsia is characterized by little to no risk of preeclampsia-related adverse outcomes, other than iatrogenic prematurity. Incorporation of angiogenic biomarkers in the evaluation of preeclampsia may allow accurate and early identification of severe disease.
引用
收藏
页码:189 / 201
页数:13
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