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Preeclamptic Patients and Pentraxin 3 & Lipoprotein-associated Phospholipase A2

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Povezava se shrani v odložišče
StanjeDokončano
Sponzorji
Kanuni Sultan Suleyman Training and Research Hospital

Ključne besede

Povzetek

In particular, pentraxine 3 (PTX3) molecule was assumed to have a prognostic value in acute myocardial infarction.In patients affected by acute myocardial infarction, early plasma elevation of PTX3 appears to predict a worse outcome in these patients in the longer term.
The inflammatory basis of preeclampsia resembles an atherogenic process.It is planned to investigate the role of these two molecules in endothelial dysfunction typical of preeclampsia.
The level of circulating PTX3 and Lp-PLA2 in preeclamptic patients and their serum levels according to the severity of preeclampsia and presence of IUGR, and comparison with the control group without preeclampsia and It is planned to investigate the cut-off values and sensitivity and specificity of both molecules together and separately in preeclampsia.

Datumi

Nazadnje preverjeno: 04/30/2020
Prvič predloženo: 01/19/2020
Predviden vpis oddan: 01/22/2020
Prvič objavljeno: 01/26/2020
Zadnja posodobitev oddana: 05/20/2020
Zadnja posodobitev objavljena: 05/21/2020
Dejanski datum začetka študija: 01/19/2020
Predvideni datum primarnega zaključka: 05/19/2020
Predvideni datum zaključka študije: 05/19/2020

Stanje ali bolezen

Pre-Eclampsia

Intervencija / zdravljenje

Diagnostic Test: Pentraxin 3 ; new biomarker

Diagnostic Test: Lipoprotein-associated phospholipase A2 ; new biomarker

Faza

-

Skupine rok

RokaIntervencija / zdravljenje
healthy pregnant women
Blood samples taken from 40 healthy pregnant women will be obtained by taking patient consent forms and storing their serum at -80 degrees. Then, serum Pentraxin 3 and Lp-PLA2 levels will be checked in these blood by ELISA method. this group will be the control group.
preeclamptic pregnant women
Blood samples taken from 40 preeclamptic pregnant women will be obtained by taking patient consent forms and storing their serum at -80 degrees. Then, serum Pentraxin 3 and Lp-PLA2 levels will be checked in these blood by ELISA method. this group will be the study group.

Merila upravičenosti

Starost, primerna za študij 18 Years Za 18 Years
Spol, upravičen do študijaFemale
Metoda vzorčenjaProbability Sample
Sprejema zdrave prostovoljceDa
Merila

Inclusion Criteria:

- pregnant women diagnosed with preeclampsia; The blood pressure and proteinuria (at least ≥ 300 mg in urine for 24 hours) will be established before the 20th week of gestation in normotensive pregnancies with an interval of 6 hours.

- Those who have Grand mal convulsions; other causes of convulsions and exclusion of coma were defined as having seizures for the first time after 20 weeks of gestation and 48-72 hours after delivery.

- The diagnosis of HELLP syndrome will be confirmed by intravascular hemolysis. (Abnormal peripheral smear and / or abnormal bilirubin values), high liver enzymes (high serum aspartate transaminase levels [AST], alanine transferase [ALT] and lactate dehydrogenase [LDH] üst 2 upper level) and low platelet count (<100 000 / mm3)

- healthy pregnant women without additional disease for the control group

Exclusion Criteria:

- Maternal diabetes

- Kidney disease

- Cardiovascular disease

- Neurological disease

- drug use history

- Hematological and immunological disease

- The presence of any infection

- Fetal anomaly

- In utero dead fetus

Izid

Primarni izidni ukrepi

1. study group [1 week]

preeclampsia in pregnant women; in the study group; serum Pentraxin 3 & Lipoprotein-associated phospholipase A levels It will be investigated whether these parameters observed in pregnant women with preeclampsia vary. Thus, it will be tried to be shown that these new markers may have a place in predicting the risk of preeclampsia

2. control group [1 week]

in healthy pregnant women; in the control group; serum Pentraxin 3 & Lipoprotein-associated phospholipase A levels The values of these new parameters in healthy pregnants that constitute the control group will be determined and it will be understood whether there is a difference with the pregnants who developed the preeclampsia

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