CC BY-NC-ND 4.0 · Asian J Neurosurg 2023; 18(01): 108-116
DOI: 10.1055/s-0043-1760859
Original Article

Association of ABO Blood Group with Delayed Cerebral Ischemia and Clinical Outcomes Following Aneurysmal Subarachnoid Hemorrhage in Pakistan

Saleha Azeem*
1   King Edward Medical University, Lahore, Pakistan
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
2   Wolfson School of Medicine, University of Glasgow, Scotland, United Kingdom
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
Usman Ahmad Kamboh
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
Muhammad Asif Raza
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
1   King Edward Medical University, Lahore, Pakistan
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
1   King Edward Medical University, Lahore, Pakistan
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
Nabeel Choudhary
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
,
Syed Shahzad Hussain
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
4   Department of Neurosurgery, Gujranwala Medical College, Gujranwala, Pakistan
,
Naveed Ashraf
3   Department of Neurosurgery, Allama Iqbal Medical College, Jinnah Hospital Lahore, Pakistan
› Author Affiliations
Funding None.

Abstract

Background The ABO blood type, due to its various hemostaseologic properties, has been associated with several vascular diseases, including aneurysmal subarachnoid hemorrhage (aSAH). However, the role of ABO blood type in delayed cerebral ischemia (DCI) onset and other clinical outcomes after aSAH is largely unexplored. This study aimed to investigate the association between ABO blood type and outcomes after aSAH, primarily DCI.

Methods A retrospective analysis was made on the data collected from 175 aSAH patients at a tertiary supraregional neurosurgery department over 5 years. Socio-demographic factors, clinical variables (DCI, mFG, WFNS grade, and Glasgow Outcome Scale at discharge), EVD placement, and aneurysm size were analyzed for their association with ABO blood type.

Results DCI was reported in 25% of patients with ‘O’ blood type and 9.6% with ‘non-O’ blood type. A stepwise logistic regression model showed that after adjusting for BMI, mFG, WFNS grade, and EVD placement, ‘O’ type blood group was an independent risk factor for DCI, greatly increasing the risk of DCI as compared to ‘non-O’ type groups (OR = 3.27, 95% CI: 1.21–8.82).

Conclusion This study provides evidence that individuals with ‘O’ blood type may have a higher risk of DCI onset after aSAH. However, further studies are essential to address the limitations of our work and confirm our findings.

Note

Data from this work has been previously presented at the following conferences:


35th Annual Meeting of the Pakistan Society of Neurosurgeons held from November 11 to November 13, 2023, at King Edward Medical University, Lahore, Pakistan


62nd Annual Scientific Meeting of the British Society of Haematology held from April 3 to April 5, 2022, at the Manchester Central Convention Complex, Manchester, England, United Kingdom


Ethical Approval

The study was approved by our ethical review board.


* These authors contributed equally and retain the first authorship.




Publication History

Article published online:
15 March 2023

© 2023. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Etminan N, Chang H-S, Hackenberg K. et al. Worldwide incidence of aneurysmal subarachnoid hemorrhage according to region, time period, blood pressure, and smoking prevalence in the population: a systematic review and meta-analysis. JAMA Neurol 2019; 76 (05) 588-597
  • 2 Kundra S, Mahendru V, Gupta V, Choudhary AK. Principles of neuroanesthesia in aneurysmal subarachnoid hemorrhage. J Anaesthesiol Clin Pharmacol 2014; 30 (03) 328-337
  • 3 Edlow JA, Caplan LR. Avoiding pitfalls in the diagnosis of subarachnoid hemorrhage. N Engl J Med 2000; 342 (01) 29-36
  • 4 Lawton MT, Vates GE. Subarachnoid hemorrhage. N Engl J Med 2017; 377 (03) 257-266
  • 5 de Oliveira Manoel AL, Jaja BN, Germans MR. et al; SAHIT collaborators. The VASOGRADE: a simple grading scale for prediction of delayed cerebral ischemia after subarachnoid hemorrhage. Stroke 2015; 46 (07) 1826-1831
  • 6 Lai PMR, Gormley WB, Patel N, Frerichs KU, Aziz-Sultan MA, Du R. Age-dependent radiographic vasospasm and delayed cerebral ischemia in women after aneurysmal subarachnoid hemorrhage. World Neurosurg 2019; 130: e230-e235
  • 7 de Rooij NK, Rinkel GJ, Dankbaar JW, Frijns CJ. Delayed cerebral ischemia after subarachnoid hemorrhage: a systematic review of clinical, laboratory, and radiological predictors. Stroke 2013; 44 (01) 43-54
  • 8 McGirt MJ, Mavropoulos JC, McGirt LY. et al. Leukocytosis as an independent risk factor for cerebral vasospasm following aneurysmal subarachnoid hemorrhage. J Neurosurg 2003; 98 (06) 1222-1226
  • 9 Abegaz SB. Human ABO blood groups and their associations with different diseases. BioMed Res Int 2021; 2021: 6629060
  • 10 Ward M, Doran J, Paskhover B, Mammis A. The 50 most cited articles in invasive neuromodulation. World Neurosurg 2018; 114: e240-e246
  • 11 Pluta RM. RETRACTED CHAPTER: Dysfunction of nitric oxide synthases as a cause and therapeutic target in delayed cerebral vasospasm after SAH. Acta Neurochir Suppl (Wien) 2008; 104: 139-147
  • 12 Wu O, Bayoumi N, Vickers MA, Clark P. ABO(H) blood groups and vascular disease: a systematic review and meta-analysis. J Thromb Haemost 2008; 6 (01) 62-69
  • 13 Siroya HL, Devi BI, Aripirala P. et al. Patients with invasive tumors and eNOS gene polymorphisms with subarachnoid hemorrhage tend to have poorer prognosis. Asian J Neurosurg 2022; 17 (02) 199-208
  • 14 Franchini M, Lippi G. Relative risks of thrombosis and bleeding in different ABO blood groups. Semin Thromb Hemost 2016; 42 (02) 112-117 DOI: 10.1055/s-0035-1564832.
  • 15 Zakai NA, Judd SE, Alexander K. et al. ABO blood type and stroke risk: the reasons for geographic and racial differences in stroke study. J Thromb Haemost 2014; 12 (04) 564-570
  • 16 Dubinski D, Won SY, Behmanesh B. et al. Influence of ABO blood type on the outcome after non-aneurysmal subarachnoid hemorrhage. Acta Neurochir (Wien) 2018; 160 (04) 761-766
  • 17 Dubinski D, Won S-Y, Konczalla J. et al. The role of ABO blood group in cerebral vasospasm, associated intracranial hemorrhage, and delayed cerebral ischemia in 470 patients with subarachnoid hemorrhage. World Neurosurg 2017; 97: 532-537
  • 18 Unda SR, Vats T, Garza R, Cezaryirli P, Altschul DJ. Role of ABO blood type in delayed cerebral ischemia onset and clinical outcomes after aneurysmal subarachnoid hemorrhage in an ethnic minority urban population. Surg Neurol Int 2020; 11: 108 DOI: 10.25259/SNI_10_2020.
  • 19 Richards O, Cromie KJ, Akhunbay-Fudge C. et al. ABO blood group in aneurysmal subarachnoid haemorrhage-a pilot study. Acta Neurochir (Wien) 2022; 164 (02) 507-515
  • 20 Vergouwen MD, Vermeulen M, van Gijn J. et al. Definition of delayed cerebral ischemia after aneurysmal subarachnoid hemorrhage as an outcome event in clinical trials and observational studies: proposal of a multidisciplinary research group. Stroke 2010; 41 (10) 2391-2395
  • 21 Akaike H. A new look at the statistical model identification.. IEEE Trans Automat Contr. IEEE Trans Automat Contr 1974; AC-19 (119) 716-723
  • 22 Anzalone CL, Glasgow AE, Van Gompel JJ, Carlson ML. Racial differences in disease presentation and management of intracranial meningioma. J Neurol Surg B Skull Base 2019; 80 (06) 555-561
  • 23 Kurian AK, Cardarelli KM. Racial and ethnic differences in cardiovascular disease risk factors: a systematic review. Ethn Dis 2007; 17 (01) 143-152
  • 24 Post WS, Watson KE, Hansen S. et al. Racial and ethnic differences in all-cause and cardiovascular disease mortality: the MESA study. Circulation 2022; 146 (03) 229-239
  • 25 Bir SC, Bollam P, Nanda A. Distribution of ABO blood groups in the patients with intracranial aneurysm and association of different risk factors with particular blood type. Asian J Neurosurg 2015; 10 (03) 153-157
  • 26 Tatar Aksoy H, Eras Z, Canpolat FE, Dilmen U. The association between neonatal ABO blood group and intraventricular hemorrhage in extremely low birth weight infants. J Thromb Haemost 2013; 11 (11) 2074-2075
  • 27 Groot HE, Villegas Sierra LE, Said MA, Lipsic E, Karper JC, van der Harst P. Genetically determined ABO blood group and its associations with health and disease. Arterioscler Thromb Vasc Biol 2020; 40 (03) 830-838
  • 28 Franchini M, Mannucci PM. Von Willebrand factor: another janus-faced hemostasis protein. Semin Thromb Hemost 2008; 34 (07) 663-669 DOI: 10.1055/s-0028-1104545.
  • 29 Zabaneh D, Gaunt TR, Kumari M. et al. Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip. Ann Hum Genet 2011; 75 (04) 456-467
  • 30 Zhang H, Mooney CJ, Reilly MP. ABO blood groups and cardiovascular diseases. Int J Vasc Med 2012; 2012: 641917
  • 31 Gill JC, Endres-Brooks J, Bauer PJ, Marks Jr WJ, Montgomery RR. The effect of ABO blood group on the diagnosis of von Willebrand disease. Blood 1987; 69 (06) 1691-1695
  • 32 Sodetz JM, Paulson JC, McKee PA. Carbohydrate composition and identification of blood group A, B, and H oligosaccharide structures on human factor VIII/von Willebrand factor. J Biol Chem 1979; 254 (21) 10754-10760
  • 33 Jenkins PV, O'Donnell JS. ABO blood group determines plasma von Willebrand factor levels: a biologic function after all?. Transfusion 2006; 46 (10) 1836-1844
  • 34 Koster T, Blann AD, Briët E, Vandenbroucke JP, Rosendaal FR. Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis. Lancet 1995; 345 (8943): 152-155
  • 35 Liu X, Miller MJ, Joshi MS, Sadowska-Krowicka H, Clark DA, Lancaster JR. Diffusion-limited reaction of free nitric oxide with erythrocytes. J Biol Chem 1998; 273 (30) 18709-18713
  • 36 Damodara N, Amuluru K, Nuoman R. et al. Body mass index and overall outcome following subarachnoid hemorrhage: an obesity paradox?. World Neurosurg 2020; 144: e679-e684
  • 37 Juvela S, Siironen J, Kuhmonen J. Hyperglycemia, excess weight, and history of hypertension as risk factors for poor outcome and cerebral infarction after aneurysmal subarachnoid hemorrhage. J Neurosurg 2005; 102 (06) 998-1003
  • 38 Frontera JA, Claassen J, Schmidt JM. et al. Prediction of symptomatic vasospasm after subarachnoid hemorrhage: the modified fisher scale. Neurosurgery 2006; 59 (01) 21-27 , discussion 21–27
  • 39 Aggarwal A, Dhandapani S, Praneeth K. et al. Comparative evaluation of H&H and WFNS grading scales with modified H&H (sans systemic disease): a study on 1000 patients with subarachnoid hemorrhage. Neurosurg Rev 2018; 41 (01) 241-247
  • 40 Chung DY, Mayer SA, Rordorf GA. External ventricular drains after subarachnoid hemorrhage: is less more?. Neurocrit Care 2018; 28 (02) 157-161