FIRST 5-DAYS FOLLOW-UP AND CORRELATION STUDY BETWEEN URINARY CYSTEINYL LEUKO TRIENES AND EDEMA VALUES IN PRIMARY SPONTANEOUS SUPRATENTORIAL INTRACEREBRAL HEMO RRHAGE

Background: After intracerebral hemorrhage cysteinyl leukotrienes (C4, D4, E4) are synthetisized in the contact brain parenchyma-extravasated blood and participate in producing of edema formation. The study aim is a 5-days follow up (admittance/3thday/5thday) of urinary cysteinyl leukotrienes, hema...

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Main Authors: Dolnenec-Baneva Natalia, Nikodijevik Dijana, Petrovska-Cvetkovska Dragana, Poposka Anastasika
Format: Article
Language:English
Published: Association of medical doctors Sanamed Novi Pazar 2014-07-01
Series:Sanamed
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Online Access:http://www.sanamed.rs/sanamed_pdf/sanamed_9_2/Dolnenec_Baneva_Natalija.pdf
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Summary:Background: After intracerebral hemorrhage cysteinyl leukotrienes (C4, D4, E4) are synthetisized in the contact brain parenchyma-extravasated blood and participate in producing of edema formation. The study aim is a 5-days follow up (admittance/3thday/5thday) of urinary cysteinyl leukotrienes, hematoma and edema volume in patients with primary spontaneous supratentorial intracerebral hemorrhage and to determine the relationship: edema/haematoma and edema/leuko trienes. Methods: An enzyme immunoassay for leukotrienes measuring in the urine samples from 62 patients with hemorrhage during the first 5 days ( admittance/3thday/5thday) and 80 health controls is used. Hematoma and edema volume is visualised and measured by computed-tomography. Results: Admission values of leukotrienes were significantly higher in the hemorrhagic patients (min =268.61; max = 5787.36; mean = 1842.20 ± 1413.19 pg/ml/mg creatinine) versus control subjects (min =297.8; max = 1684.2; mean = 918.6 ± 332) (p < 0.001). Significant leukotrienes excretion dynamism (mean:1842.20 ± 1413.19; 1181.54 ± 906.16; 982.30 ± 774.24pg/ml/mg creatinine) is found in hemorrhagic patients during 5 day-follow up (admittance/3thday for p < 0.001; the 3thday/5thday for p < 0.05). The followed hematoma volume (mean: 13.05 ± 14.49; 13.13 ± 14.66; 12.99 ±14.73 cm3) for all three periods of examination did not show significance (p > 0.05). The edema (mean: 12.86 ±13.52; 22.38 ± 21.10; 28.45 ± 29.41 cm3) showed very high significance (p < 0.001). At admitance and on the 5th day nonsignificant positive correlation (r = 0.4; p >0.05) of moderate strength is found between edema and hematoma; and significant positive correlation (r = 0.6; p < 0.05) of moderate to high strength at the 3thday. Between leukotrienes and edema, the coefficient of correlation r = – 0.1 (p > 0.05) at admittance, r = – 0.05 (p >0.05) on the 3th day (nonexistence of linear correlation, the sign minus presents their tendency for the opposite movement in their values) and r = 0.2 (p > 0.05) on the 5thday are found (positive linear nonsignificant correlation of slight strength). Conclusion: Significant urinary leukotrienes excretion (a brain capacity for significant leukotrienes synthesis) and significant edema progression versus constant haematoma are found. The edema size followed the hematoma size of moderate extent. The edema showed an inverse dependence of the leukotrienes (atendency for opposite movement of their values), the high leukotrienes values at admittance bring to greater edema volume on the third/the fifth day, respectively. Elevated cysteinyl leukotrienes synthesis and the elevated edema could point to cause-effective relationship between them establishing the leukotrienes as an edema promotive-factor in intracerebral haemorrhage.
ISSN:1452-662X
2217-8171