Carotid artery elongation (carotid dolichoarteriopathy): some features of the structure and hemodynamics
https://doi.org/10.24835/1607-0763-1396
Abstract
The purpose of the study. Multimodal study of the state of the brachiocephalic arteries, with assessment of blood flow in the extra- and intracranial portions of the carotid arteries and brain perfusion, as well as the structure of the brain in patients with different types of elongation of the carotid arteries (ECA).
Material and methods. The data of examinations of 79 patients (45 men (57.0%, average age – 61.0 ± 10.1 years) and 34 women (43.0%, 65.3 ± 13.6 years), average age 62.8 ± 11.8 years) during the year after ischemic stroke in posterior circulation were analyzed. ECA was verified by multispiral computed tomographic angiography (msCTA) in 44 patients (55.7% of the total number of cases), the control group was selected by gender and age with “case-control” elements and consisted of 35 (44.3%) patients without a mustache. All underwent msCTA of the thoracic aorta and BCA and CT perfusion examination, magnetic resonance imaging of the brain, duplex scanning of BCA and transcranial duplex scanning, transthoracic echocardiography, transcranial Doppler monitoring with microembolodetection.
Results. We have registered intergroup differences, which can be divided into structural and functional. The former include: higher aortic arch location in patients with DCA: ThII – 6.3% vs. 0%, ThIII – 43% vs. 0%; ThIV – 28.1% vs. 62.9%* and ThV 21.9% vs. 37.1% (p < 0.0005); lower values of cervical spine height (114.70 ± 11.03 mm, vs. 120.46 ± 9.75 mm, p = 0.022), greater absolute length of the ICA (on the right – 101.32 ± 14.59 mm vs. 85.06 ± 12.07 mm, p < 0.0005; on the left – 100.00 ± 14.03 mm vs. 84.66 ± 12.63 mm, p < 0.0005). The presence of ECA was associated (p < 0.05) with a higher frequency of vertebral artery elongation. The severity of small vessel disease during MRI in individuals with ECA was slightly higher (not at the trend level, p = 0.076). Functional differences consisted in the registration of lower (p = 0.019) values of the end diastolic velocity in M1 of the middle cerebral arteries. The values of some perfusion indices in the blood supply of elongation arteries were lower than in persons without ECA. There were no cases of registration of microembolic signals in the ECA patients examined by us.
Conclusion. In the individuals with ECA we examined, a complex of anatomical and hemodynamic features was determined, which, both individually and collectively, cannot lead to a decrease in the level of blood flow or be a source of arterio-arterial embolism in the carotid system, regardless of the configuration of the ICA.
About the Authors
D. A. GolovinRussian Federation
Denis A. Golovin – Cand. of Sci. (Med.), Senior Researcher, Federal Center of Brain Research and Neurotechnologies of the Federal Medical Biological Agency, Moscow
A. B. Berdalin
Russian Federation
Alexander B. Berdalin – Cand. of Sci. (Med.), Senior Researcher, Federal Center of Brain Research and Neurotechnologies of the Federal Medical Biological Agency, Moscow
Yu. S. Kudryavtsev
Russian Federation
Yuri S. Kudryavtsev – radiologist of Radiology and Clinical Physiology Research Center, Federal Center of Brain Research and Neurotechnologies of the Federal Medical Biological Agency, Moscow
M. B. Fedosenko
Russian Federation
Marina B. Fedosenko – doctor of ultrasound diagnostics of Radiology and Clinical Physiology Research Center, Federal Center of Brain Research and Neurotechnologies of the Federal Medical Biological Agency, Moscow
T. M. Rostovtseva
Russian Federation
Tatyana M. Rostovtseva – Researcher of Radiology and Clinical Physiology Research Center, Federal Center of Brain Research and Neurotechnologies of the Federal Medical Biological Agency, Moscow
S. E. Lelyuk
Russian Federation
Svetlana E. Lelyuk – Doct. of Sci. (Med.), Professor, Professor of the Department of Ultrasound Diagnostics, Russian Medical Academy of Continuing Professional, Moscow
V. G. Lelyuk
Russian Federation
Vladimir G. Lelyuk – Doct. of Sci. (Med.), Professor, Head of Department clinical and experimental physiology of circulatory system, ultrasound and functional diagnostics, Federal center of brain research and neurotechnologies” of the Federal Medical Biological Agency, Moscow
References
1. Schönherr U., Rupprecht H., Schweiger H., Bialasiewicz A.A. Ischämische Optikus-Neuropathie (Apoplexia papillae) und ischämische Mikroinfarkte der retinalen Nervenfaserschicht bei extremer Knickbildung der Arteria carotis interna (Carotis interna-“Kinking“) [Ischemic optic neuropathy (apoplexia papillae) and ischemic micro-infarcts of the retinal nerve fiber layer in extreme internal carotid artery kinking]. Klin. Monbl. Augenheilkd. 1990; 197 (1): 9–13. http://doi.org/10.1055/s-2008-1046235 (In German)
2. van Laarhoven C.J.H.C.M., Willemsen S.I., Klaassen J. et al.; Carotid Aneurysm Registry (CAR) study group. Carotid tortuosity is associated with extracranial carotid artery aneurysms. Quant. Imaging Med. Surg. 2022; 12 (11): 5018–5029. http://doi.org/10.21037/qims-22-89
3. Wang L., Zhao F., Wang D. et al. Pressure Drop in Tortuosity/Kinking of the Internal Carotid Artery: Simulation and Clinical Investigation. Biomed. Res. Int. 2016; 2016: 2428970. http://doi.org/10.1155/2016/2428970
4. Sun Z., Jiang D., Liu P. et al. Age-Related Tortuosity of Carotid and Vertebral Arteries: Quantitative Evaluation With MR Angiography. Front. Neurol. 2022; 13: 858805. http://doi.org/10.3389/fneur.2022.858805
5. Bernaudin F., Arnaud C., Kamdem A. et al. Incidence, kinetics, and risk factors for intra- and extracranial cerebral arteriopathies in a newborn sickle cell disease cohort early assessed by transcranial and cervical color Doppler ultrasound. Front. Neurol. 2022; 13: 846596. http://doi.org/10.3389/fneur.2022.846596
6. Buch K., Arya R., Shah B. et al. Quantitative Analysis of Extracranial Arterial Tortuosity in Patients with Sickle Cell Disease. J Neuroimaging. 2017; 27 (4): 421–427. http://doi.org/10.1111/jon.12418
7. Zeng W., Chen Y., Zhu Z. et al. Severity of white matter hyperintensities: Lesion patterns, cognition, and microstructural changes. J. Cereb. Blood Flow. Metab. 2020; 40 (12): 2454–2463. http://doi.org/10.1177/0271678X19893600
8. Morris S.A., Orbach D.B., Geva T. et al. Increased vertebral artery tortuosity index is associated with adverse outcomes in children and young adults with connective tissue disorders. Circulation. 2011; 124 (4): 388–396. http://doi.org/10.1161/CIRCULATIONAHA.110.990549
9. Weibel J., Fields W.S. Tortuosity, coiling, and kinking of the internal carotid artery. I. Etiology and radiographic anatomy. Neurology. 1965; 15: 7–18. http://doi.org/10.1212/wnl.15.1.7
10. Lelyuk V.G., Lelyuk S.E. Cerebral circulation and arterial blood pressure. M.: Real time, 2004: 142–148. ISBN 5-900080-26-9. (In Russian)
11. Golovin D.A., Rostovtseva T.M., Kudryavtsev Yu.S. et al. Carotid artery elongation (dolichoarteriopathy) and cerebral perfusion: results of a pilot study. Cardiovascular Therapy and Prevention. 2021; 20 (5): 2778. https://doi.org/10.15829/1728-8800-2021-2778 (In Russian)
12. Shang K., Chen X., Cheng C. et al. Arterial Tortuosity and Its Correlation with White Matter Hyperintensities in Acute Ischemic Stroke. Neural. Plast. 2022; 2022: 4280410. https://doi.org/10.1155/2022/4280410
13. Yin L., Li Q., Zhang L. et al. Correlation between cervical artery kinking and white matter lesions. Clin. Neurol. Neurosurg. 2017; 157: 51–54. https://doi.org/10.1016/j.clineuro.2017.04.003
14. Liu J., Ke X., Lai Q. Increased tortuosity of bilateral distal internal carotid artery is associated with white matter hyperintensities. Acta. Radiol. 2021; 62 (4): 515–523. https://doi.org/10.1177/0284185120932386
15. Yu K., Zhong T., Li L. et al. Significant Association between Carotid Artery Kinking and Leukoaraiosis in Middle-Aged and Elderly Chinese Patients. J. Stroke Cerebrovasc. Dis. 2015; 24 (5): 1025–1031. https://doi.org/10.1016/j.jstrokecerebrovasdis.2014.12.030
16. Konstas A.A., Goldmakher G.V., Lee T.Y., Lev M.H. Theoretic basis and technical implementations of CT perfusion in acute ischemic stroke, part 1: Theoretic basis. Am. J. Neuroradiol. 2009; 30 (4): 662–668. https://doi.org/10.3174/ajnr.A1487
17. d'Ostrevy N., Ardellier F.D., Cassagnes L. et al. The apex of the aortic arch backshifts with aging. Surg. Radiol. Anat. 2017; 39 (7): 703–710. https://doi.org/10.1007/s00276-016-1792-9
18. Boufi M., Guivier-Curien C., Loundou A.D. et al. Morphological Analysis of Healthy Aortic Arch. Eur. J. Vasc. Endovasc. Surg. 2017; 53 (5): 663–670. https://doi.org/10.1016/j.ejvs.2017.02.023
19. Wang H.F., Wang D.M., Wang J.J. et al. Extracranial Internal Carotid Artery Tortuosity and Body Mass Index. Front. Neurol. 2017; 8: 508. https://doi.org/10.3389/fneur.2017.00508
20. Humphrey J.D. Mechanisms of Vascular Remodeling in Hypertension. Am. J. Hypertens. 2021; 34 (5): 432–441. https://doi.org/10.1093/ajh/hpaa195
21. Yu J., Qu L., Xu B. et al. Current Understanding of Dolichoarteriopathies of the Internal Carotid Artery: A Review. Int. J. Med. Sci. 2017; 14 (8): 772–784. https://doi.org/10.7150/ijms.19229
22. Aghasadeghi F., Dehghan A. Evaluation of the association between the internal carotid artery and vertebral artery tortuosity and acute ischemic stroke using tortuosity index. Vascular. 2022: 17085381221140163. https://doi.org/10.1177/17085381221140163
23. Liu Y.T., Zhang Z.M., Li M.L. et al. Association of carotid artery geometries with middle cerebral artery atherosclerosis. Atherosclerosis. 2022; 352: 27–34. https://doi.org/10.1016/j.atherosclerosis.2022.05.016
24.
Review
For citations:
Golovin D.A., Berdalin A.B., Kudryavtsev Yu.S., Fedosenko M.B., Rostovtseva T.M., Lelyuk S.E., Lelyuk V.G. Carotid artery elongation (carotid dolichoarteriopathy): some features of the structure and hemodynamics. Medical Visualization. 2024;28(4):33-46. (In Russ.) https://doi.org/10.24835/1607-0763-1396