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Content of Bali Medical Journal

Vol. 5 No. 1 2016

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Analysis of Glial Fibrillary Acidic Protein (GFAP) Serum Levels on

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Suzy Indharty, Iskandar Japardi, Muhammad Fadhli

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As’ad

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Bali Medical Journal (Bali Med J) 2016, Volume 5, Number 1: 56-60 P-ISSN.2089-1180, E-ISSN.2302-2914

Open access: www.balimedicaljournal.org and www.ojs.unud.ac.id 56

Analysis of Glial Fibrillary Acidic Protein (GFAP) Serum Levels on Spontaneous Intracerebral Hemorrhage Non-Lesion Patients

Suzy Indharty, Iskandar Japardi, Muhammad Fadhli

Master of Clinical Medicine, Surgical Nerve Specialist, Medical Faculty North Sumatra University.

Corresponding: E-mail: Dokterfadhlimuhammad@gmail.com

Background: Stroke is one of the root causes of brain disorders at the height of the productive age and ranks second cause of death after heart disease in most countries in the world. Fairly large-scale study conducted by ASNA (ASEAN Neurological Association) in 28 Hospitals in Indonesia. This study was conducted in patients with acute stroke who were treated in hospital (hospital-based study) and conducted a survey of factors - risk factors, treatment duration and mortality and morbidity. Method:

This is a cross sectional study, with intracerebral hemorrhage Head CT scan examination then examined serum levels of plasma GFAP her at the time of patient entry from RSUP. H. Adam Malik Medan from March 2014 -May 2014. Results: In this research, we found the frequency of male patients as many (62.5%), while as many women (37.5%). Predominant age range in patients encountered in this study were 46-51 years old and are the dominant ethnic Batak tribe (43.8%). Conclusion: There were no significant differences between groups in serum GFAP levels with bleeding volume ≥ 30 cc compared to those with bleeding volume <30 cc (p = 0.599). GFAP is a biomarker to distinguish whether stroke patients including intracerebral hemorrhage or ischemic stroke Further longitudinal study would be needed to confirm the role.

Keywords:Stroke, GFAP, Intracerebral hemorrhage.

DOI: 10.15562/bmj.v5i1.163

Cite This Article: Indharty, S., Japardi, I., Fadhli, M. 2016. Analysis of Glial Fibrillary Acidic Protein (GFAP) Serum Levels on Spontaneous Intracerebral Hemorrhage Non-Lesion Patients. Bali Medical Journal 5(1): 56-60. DOI:10.15562/bmj.v5i1.163

INTRODUCTION

Stroke is one of the causes of brain disorders at the height of the productive age and ranks second cause of death after heart disease in most countries in the world. Fairly large-scale study conducted by ASNA (ASEAN Neurological Association) in 28 Hospitals in Indonesia. This study was conducted in patients with acute stroke who were treated in hospital (hospital-based study) and conducted a survey of factors - risk factors, treatment duration and mortality and morbidity. The results showed that patients with more men than women with a profile under 45 years of age in quite a lot of that is 11.8%, age 45-64 years amounted to 54.7% and over the age of 65 years 33.5%. Neurological biomarkers showed clinically significant in some circumstances include head injury, anoxia, subarachnoid bleeding and ischemic stroke.1,2

Corresponding author:

Muhammad Fadhli

Address: Master of Clinical Medicine, Surgical Nerve Specialist, Medical Faculty North Sumatra University.

Email: Dokterfadhlimuhammad@gmail.com

Biological markers are also very useful in cases of acute stroke. Examination of blood samples examined by a particular method allows to quickly differentiate ischemic stroke and intracerebral hemorrhage in order to provide the possibility for immediate intervention. Furthermore, biological markers may provide prognostic information and may identify patients who have a high risk of side effects specific therapy. Glial fibrillary acidic protein (GFAP) is a specific protein filament in the brain which appears immediately on astrocytes. The new examination identified as a biological marker of intracerebral hemorrhage in the acute phase of stroke. Has an important role in maintaining the size and motility of astrocytic processes and contribute to the structure of white matter, myelination and integrity of the blood brain barrier. High levels of GFAP are found in specific parts of the brain.3-9

METHODS

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-Bali Medical Journal (-Bali Med J) 2016, Volume 5, Number 1: 56-60 P-ISSN.2089-1180, E-ISSN.2302-2914

Open access: www.balimedicaljournal.org and www.ojs.unud.ac.id 57

May 2014. The BC patients must fulfill the criteria: Patients who suffer from ICH all sexes, aged adult (over 18 years), when the incident until arriving at the hospital less than 48 hours, the patient came directly from the scene and has not received any treatment, and the results of a CT scan of the brain of ICH. T-Test analysis was performed between those variable (GFAP levels with bleeding volume ≥ 30 cc compared to those with bleeding volume <30 cc) with p value of 0,005.10-13

RESULT

In this research, we found the frequency of male patients as many (62.5%), while as many women (37.5%). Predominant age range in patients encountered in this study were 46-51 years old and are the dominant ethnic Batak tribe (43.8%).14 From this study it was found that the location of bleeding most is the Basal Ganglia (34.3%). There are significant differences in serum GFAP levels among groups with ≥ 30 cc volume of bleeding compared to those with bleeding volume <30 cc (p = 0.599). This research also obtained mortality rate is high enough that as many as 19 research subjects died (59.4%) and only 13 research subjects who survived (40.6%). The results of this study are expected to become an input for further research that will be useful for the treatment of patients with intracerebral hemorrhage.15-17

Table 1 Demographic characteristics Research Subjects

Analysis of serum GFAP levels between men and women

Figure 2

Analysis of serum GFAP levels based on ethnicity

Table 2. Analysis of serum GFAP levels between men and women

Gender N Mean Median SD Range p

Male 20 0,5919 0,4493 0,4767 0,1100 – 1,9200 0,235* Female 12 2,0499 0,5750 2,3703 0,0800 – 6,3000

Table 3. Analysis of serum GFAP levels based on ethnicity

Ethnicity N Mean Median SD Range p

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Bali Medical Journal (Bali Med J) 2016, Volume 5, Number 1: 56-60 P-ISSN.2089-1180, E-ISSN.2302-2914

Open access: www.balimedicaljournal.org and www.ojs.unud.ac.id 58

Age N Mean Median SD Range p

34 – 39 5 1,1352 0,5200 1,7584 0,1100 – 4,2500

0,100* 40 – 45 6 0,4460 0,4493 0,0320 0,4000 – 0,4800

46 – 51 11 0,5125 0,3400 0,5046 0,0800 – 1,9200 52 – 57 7 2,0444 1,3000 2,1397 0,1500 – 5,6900 58 – 64 2 2,7121 0,9764 3,1077 0,8600 – 6,3000

Table 4. Analysis of serum GFAP levels by Location Bleeding

Bleeding Location N Mean Median SD Range p

Ganglia Basal 11 0,7984 0,4800 0,5704 0,0800 – 1,9200

0,230* Lobar 9 0,3969 0,4300 0,2167 0,1100 – 0,6700

Thalamus 6 1,2813 0,3316 2,1754 0,1500 – 5,6900 Cerebellum 4 3,8145 4,3127 2,5036 0,3300 – 6,3000 Pons 2 0,5682 0,5682 0,5772 0,1600 – 0,9800

Table 5. Analysis of serum GFAP levels by Volume Hemorrhage

Volume Hemorrhage N Mean Median SD Range p

< 30 cc 20 1,4402 0,4750 1,97278 0,08 – 6,30 0,599* ≥ 30 cc 12 0,6360 0,4493 0,54550 0,11 – 1,92

Table 6. Analysis of serum GFAP levels by Outcome

Outcome N Mean Median SD Range p

Alive 13 1,1958 0,7469 1,6285 0,1500 – 6,3000 0,431* Death 19 1,0995 0,4300 1,6695 0,0800 – 5,6900

* Uji Mann-Whitney U

Figure 3

Analysis of serum GFAP levels with Age

Figure 4

Analysis of serum GFAP levels by Location Bleeding

Figure 5

Analysis of serum GFAP levels by Volume Hemorrhage

Figure 6

Analysis of serum GFAP levels by Volume Hemorrhage

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Bali Medical Journal (Bali Med J) 2016, Volume 5, Number 1: 56-60 P-ISSN.2089-1180, E-ISSN.2302-2914

Open access: www.balimedicaljournal.org and www.ojs.unud.ac.id 59

From this study it was found that the location of bleeding most is the Basal Ganglia (34.3%). There are significant differences in serum GFAP levels among groups with ≥ 30 cc volume of bleeding compared to those with bleeding volume <30 cc (p = 0.599). This research also obtained mortality rate is high enough that as many as 19 research subjects died (59.4%) and only 13 research subjects who survived (40.6%). The results of this study are expected to become an input for further research that will be useful for the treatment of patients with intracerebral hemorrhage.18-21

CONCLUSIONS

There were no significant differences between groups in serum GFAP levels with bleeding volume ≥ 30 cc compared to those with bleeding volume <30 cc (p = 0.599). GFAP is a biomarker to distinguish whether stroke patients including intracerebral hemorrhage or ischemic stroke Further longitudinal study would be needed to confirm thus role.

REFERENCES

1. Abadier, M.Z.; Eliwa, G.H.; Mohammed, M.A.; Ahmed, Z.M.; Abdel Salam, O.A. 2012. Plasma Glial Fibrillary Acidic Protein, D-Dimer and S100β Protein: A Panel for Differential Diagnosis of Acute Stroke. Journal of American Science. 8(5): 267-272.

2. Brahmachari, S.; Fung, Y.K.; Pahan, K. 2006.Induction of Glial Fibrillary Acidic Protein Expression in Astrocytes by Nitric Oxide. The Journal of Neuroscience. 26(18): 4930-4939. 3. Caplan, L.R. 2000. Caplan’s Stroke: A Clinical

Approach. 3rd ed. Butterworth-Heinemann. Boston.

4. Carhuapoma, J.R.; Mayer, S.A.; Hanley, D.F. 2010.Intracerebral Hemorrhage. Cambridge University Press. New York.

5. Dvorak, F.; Haberer, I.; Sitzer, M.; Foerch, C. 2009.Characterisation of the Diagnostic Window of Serum Glial Fibrillary Acidic Protein for the Differentiation of Intracerebral Hemorrhage and Ischemic Stroke. Cerebrovascular Dis. 27: 37-41.

6. Foerch, C.; Curdt, I.; Yan, B.; Dvorak F.; Hermans, M.; Berkefeld, J. et al. 2006. Serum Glial Fibrillary Acidic Protein as A Biomarker for Intracerebral Hemorrhage in Patients with Acute Stroke. J Neurol Neurosurg Psychiatry.77: 181-184.

7. Foerch, C.; Niessner, M.; Back, T.; Bauerle, M.; Marchis, G.M.D. et al. 2012.Diagnostic Accuracy of Plasma Glial Fibrillary Acidic Protein for Differentiating Intracerebral Hemorrhage and Cerebral Ischemia in Patients with Symptoms of Acute Stroke.Clinical Chemistry.58: 1-9.

8. Gilroy, J. 2000. Basic Neurology.3rd ed. McGraw-Hill. New York.

9. Hol.J.M.EM. 2011.GFAP in Health and Disease.Progress in Neurobiology.93: 421-443. 10.Johnson, M.H. and Kubal, W.S. 1999. Stroke. In:

Lee, S.H., Rao, K.C.V.G. and Zimmermann, R.A. (eds) Cranial MRI and CT. 4th ed. Pp 557-598. McGraw-Hill. New York.

11.Kamchatnov, P.R.; Chugunov.A.V.; Ruleva, N.Y.; Dugin, S.F.; Daria, A.B. et al. 2010.Autoantibodies to GFAP and dopamine in Patients with Acute and Chronic Cerebrovascular Disorders. Health. 2(12): 1366-1371.

12.Misbach, J. 1999. Stroke : Aspek Diagnostik, Patofisiologi,Manajemen. Balai Penerbit FK-UI. Jakarta.

13.Marginean I.C.; Stanca, D.M.; Vacaras, V.; Margiean, M.; Muresanu, D.F. et al. 2011. Plasmatic Marker in Hemorragic Stroke. Journal of Medicine and Life. 4(2) : 148-150.

14.Mayer, C.A.; Brunkhorst, R.; Niessner, M.; Pfeilschifter, W. et al. 2013. Blood Levels of Glial Fibrillary Acidic Protein (GFAP) in Patients with Neurological Diseases. Plos One. 8(4) : 1-5.

15.Pekny, M.; Johansson, C.B.; Eliasson, C.; Stakeberg, J.; Wallen, A.; Perlmann, T. et al. 1999. Abnormal Reaction to Central Nervous System Injury in Mice Lacking Glial Fibrillary Acidic Protein and Vimentin. The Journal of

18.Ramachandran, Sharanya. Reverse Shoulder Prosthesis: Review Dari Fitur Imaging Dan Komplikasinya. Intisari Sains Medis, [S.l.], v. 4, n. 1, sep. 2016. ISSN 2503-3638. Available at: <http://isainsmedis.id/ojs/index.php/ISM/article /view/54>. Date accessed: 30 apr. 2016. 19.Schiff, L.; Hadker, N.; Weiser, S.; Rausch, C.

2012. A Literature Review of The Feasibility of Glial Fibrillary Acidic Protein as A Biomarker for Stroke and Traumatic Brain Injury. Mol Diagn Ther. 16(2) : 79-92.

20.Unden, J.; Strandberg, K.; Malm, J.; Campbell, E.; Rosengren, L.; Stenflo, J. 2009. Explorative Investigation of Biormarkers of Brain Damage and Coagulation System Activation in Clinical Stroke Differentiation. J Neurol. 256 : 72-77. 21.The Wikipedia Free Encyclopedia. (2011). Glial

cell. Adelaide: Wikimedia Foundation Inc.; 1-6.

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Bali Medical Journal (Bali Med J) 2016, Volume 5, Number 1: 56-60 P-ISSN.2089-1180, E-ISSN.2302-2914

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Gambar

Table 1 Demographic characteristics Research Subjects
Table 4. Analysis of serum GFAP levels by Location Bleeding

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