<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Annals of Clinical and Experimental Neurology</journal-id><journal-title-group><journal-title xml:lang="en">Annals of Clinical and Experimental Neurology</journal-title><trans-title-group xml:lang="ru"><trans-title>Анналы клинической и экспериментальной неврологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-5473</issn><issn publication-format="electronic">2409-2533</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1283</article-id><article-id pub-id-type="doi">10.17816/ACEN.1283</article-id><article-id pub-id-type="edn">HUVVST</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Original articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Оригинальные статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Electrophysiological markers of chemotherapy-induced polyneuropathy</article-title><trans-title-group xml:lang="ru"><trans-title>Электрофизиологические маркеры химиоиндуцированной полинейропатии</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1796-0193</contrib-id><name-alternatives><name xml:lang="en"><surname>Tikhonova</surname><given-names>Olga A.</given-names></name><name xml:lang="ru"><surname>Тихонова</surname><given-names>Ольга Алексеевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>neurologist, assistant, Department of psychiatry and neurosciences</p></bio><bio xml:lang="ru"><p>врач-невролог, ассистент каф. психиатрии и нейронаук</p></bio><email>offelia78@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1004-992X</contrib-id><name-alternatives><name xml:lang="en"><surname>Druzhinina</surname><given-names>Evgeniia S.</given-names></name><name xml:lang="ru"><surname>Дружинина</surname><given-names>Евгения Сергеевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.), Associate Professor, Department of neurology, neurosurgery and medical genetics named after academician L.O. Badalyan, Faculty of pediatrics</p></bio><bio xml:lang="ru"><p>кандидат медицинских наук, доцент каф. неврологии, нейрохирургии и медицинской генетики им. акад. Л.О. Бадаляна педиатрического факультета</p></bio><email>offelia78@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6244-0867</contrib-id><name-alternatives><name xml:lang="en"><surname>Druzhinin</surname><given-names>Dmitry S.</given-names></name><name xml:lang="ru"><surname>Дружинин</surname><given-names>Дмитрий Сергеевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Dr. Sci. (Med.),<bold> </bold>Associate Professor, Department of nervous diseases with medical genetics and neurosurgery</p></bio><bio xml:lang="ru"><p>доктор медицинских наук, доцент каф. нервных болезней с медицинской генетикой и нейрохирургией</p></bio><email>offelia78@mail.ru</email><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Immanuel Kant Baltic Federal University</institution></aff><aff><institution xml:lang="ru">Балтийский федеральный университет имени Иммануила Канта</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Pirogov Russian National Research Medical University</institution></aff><aff><institution xml:lang="ru">Российский национальный исследовательский медицинский университет имени Н.И. Пирогова (Пироговский Университет)</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Yaroslavl State Medical University</institution></aff><aff><institution xml:lang="ru">Ярославский государственный медицинский университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2025-06-26" publication-format="electronic"><day>26</day><month>06</month><year>2025</year></pub-date><volume>19</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>34</fpage><lpage>40</lpage><history><date date-type="received" iso-8601-date="2025-01-31"><day>31</day><month>01</month><year>2025</year></date><date date-type="accepted" iso-8601-date="2025-04-07"><day>07</day><month>04</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, Tikhonova O.A., Druzhinina E.S., Druzhinin D.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, Тихонова О.А., Дружинина Е.С., Дружинин Д.С.</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">Tikhonova O.A., Druzhinina E.S., Druzhinin D.S.</copyright-holder><copyright-holder xml:lang="ru">Тихонова О.А., Дружинина Е.С., Дружинин Д.С.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://annaly-nevrologii.com/pathID/article/view/1283">https://annaly-nevrologii.com/pathID/article/view/1283</self-uri><abstract xml:lang="en"><p><bold>Introduction</bold><bold>. </bold>Electrophysiological testing is the gold standard for diagnosing polyneuropathy. However, its use in oncology practice for patients with chemotherapy-induced polyneuropathy (CIPN) remains limited and the value of its findings is not fully understood.</p> <p><bold>The</bold><bold> </bold><bold>study</bold><bold> </bold><bold>was</bold><bold> </bold><bold>aimed</bold> at identifying electrophysiological CIPN markers and evaluting their sensitivity and specificity.</p> <p><bold>Materials</bold><bold> </bold><bold>and</bold><bold> </bold><bold>methods</bold><bold>.</bold> The study included patients (n = 71) over 18 years of age with solid tumor presenting with polyneuritic complaints following neurotoxic therapy with platinum-based agents and taxanes. Patients with known risk factors for polyneuropathy were excluded. Electrophysiological and clinical patient data were evaluated no earlier than 3 months following chemotherapy initiation.</p> <p><bold>Results</bold><bold>. </bold>The study identified electromyographic markers: SRAR index (sural/radial ratio — the ratio between the action potential amplitudes of the sural and radial nerves) and the sural nerve action potential (SNAP), demonstrating equal sensitivity (73.7%) and high specificity (75% and 84.6%, respectively).</p> <p><bold>Conclusion</bold><bold>.</bold> Electromyographic parameters such as SRAR and SNAP sural nerve can be utilized for the diagnosis and monitoring of CIPN in daily practice.</p></abstract><trans-abstract xml:lang="ru"><p><bold>Введение. </bold>Электрофизиологическое исследование является стандартом при диагностике полинейропатии. Пока его использование ограничено в онкологической практике у пациентов с химиоиндуцированной полинейропатией (ХИПН), а ценность полученных результатов не до конца понятна.</p> <p><bold>Цель </bold>исследования — выявить электрофизиологические маркеры ХИПН и оценить их чувствительность и специфичность.</p> <p><bold>Материалы и методы.</bold> В исследование были включены пациенты (n = 71) старше 18 лет с солидными злокачественными новообразованиями, предъявляющие полиневритические жалобы после нейротоксической терапии с использованием препаратов платины и таксанов. Исключались пациенты с известными факторами риска развития полинейропатии. Изучали электрофизиологические, клинические данные пациентов не ранее чем через 3 мес после старта химиотерапии.</p> <p><bold>Результаты. </bold>В ходе исследования выявлены электромиографические маркеры: индекс SRAR (sural/radial ratio — соотношение между амплитудой потенциала действия икроножного и лучевого нервов) и потенциал действия икроножного нерва с равной чувствительностью (73,7%) и высокой специфичностью (75 и 84,6% соответственно).</p> <p><bold>Заключение.</bold> Для диагностики и мониторинга ХИПН в ежедневной практике могут использоваться электромиографические показатели, такие как SRAR и потенциал действия икроножного нерва.</p></trans-abstract><kwd-group xml:lang="en"><kwd>electroneuromyography</kwd><kwd>chemotherapy-induced polyneuropathy</kwd><kwd>markers</kwd><kwd>SRAR</kwd><kwd>cancer</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>электронейромиография</kwd><kwd>химиоиндуцированная полинейропатия</kwd><kwd>маркеры</kwd><kwd>SRAR</kwd><kwd>рак</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="ru">«Приоритет 2030» программа стратегического академического лидерства</institution></institution-wrap></funding-source></award-group></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Seretny M, Currie GL, Sena ES, et al. Incidence, prevalence, and predictors of chemotherapy-induced peripheral neuropathy: a systematic review and meta-analysis. Pain. 2014;155(12):2461–2470. doi: 10.1016/j.pain.2014.09.020</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Fuglsang-Frederiksen A, Pugdahl K. Current status on electrodiagnostic standards and guidelines in neuromuscular disorders. Clin Neurophysiol. 2011;122(3):440–455. doi: 10.1016/j.clinph.2010.06.025</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Novello BJ, Pobre T. Electrodiagnostic evaluation of peripheral neuropathy. Treasure Island; 2025.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Griffith KA, Dorsey SG, Renn CL, et al. Correspondence between neurophysiological and clinical measurements of chemotherapy‐induced peripheral neuropathy: secondary analysis of data from the CI‐PERINOMS study. J Peripher Nerv Syst. 2014;19(2):127–135. doi: 10.1111/jns5.12064</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Cho KH, Han EY, Shin JC, et al. Comparison of clinical symptoms and neurophysiological findings in patients with chemotherapy induced peripheral neuropathy. Front Neurol. 2022;13:838302. doi: 10.3389/fneur.2022.838302</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Wang M, Bandla A, Sundar R, Molassiotis A. The phenotype and value of nerve conduction studies in measuring chemotherapy-induced peripheral neuropathy: a secondary analysis of pooled data. Eur J Oncol Nurs. 2022; 60:102196. doi: 10.1016/j.ejon.2022.102196</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Супонева Н.А., Арестова А.С., Мельник Е.А. и др. Валидация шкалы суммарной оценки мышечной силы (MRC sum score) для использования у русскоязычных пациентов с хронической воспалительной демиелинизирующей полинейропатией. Нервно-мышечные болезни. 2023;13(1):68–74. Suponeva NA, Arestova AS, Melnik EA, et al. Validation of the Medical Research Council sum score (MRCss) for use in Russian-speaking patients with chronic inflammatory demyelinating polyneuropathy. Neuromuscular Diseases. 2023;13(1):68–74. doi: 10.17650/2222-8721-2023-13-1-68-74</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Mooi CS, Lee KW, Yusof Khan AHK, et al. Using biothesiometer, Neuropathy Symptom Score, and Neuropathy Disability Score for the early detection of peripheral neuropathy: a cross-sectional study. Qatar Med J. 2024;2024(3):24. doi: 10.5339/qmj.2024.24</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Using the Common Terminology Criteria for Adverse Events (CTCAE — Version 5.0) to Evaluate the Severity of Adverse Events of Anticancer Therapies. Actas Dermosifiliogr (Engl Ed). 2021;112(1):90–92. doi: 10.1016/j.ad.2019.05.009</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Stålberg E, Van Dijk H, Falck B, et al. Standards for quantification of EMG and neurography. Clin Neurophysiol. 2019;130(9):1688–1729. doi: 10.1016/j.clinph.2019.05.008</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Electromyography and neuromuscular disorders: clinical-electrodiagnostic-ultrasound correlations, Fourth Edition. J Clin Neurophysiol. 2021;38(4):e19. doi: 10.1097/WNP.0000000000000842</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Esper GJ, Nardin RA, Benatar M, et al. Sural and radial sensory responses in healthy adults: diagnostic implications for polyneuropathy. Muscle Nerve. 2005;31(5):628–632. doi: 10.1002/mus.20313</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Overbeek BUH, Van Alfen N, Bor JA, Zwarts MJ. Sural/radial nerve amplitude ratio: reference values in healthy subjects. Muscle Nerve. 2005;32(5):613–618. doi: 10.1002/mus.20421</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Rutkove SB, Kothari MJ, Raynor EM, et al. Sural/radial amplitude ratio in the diagnosis of mild axonal polyneuropathy. Muscle Nerve. 1997;20(10):1236–1241. doi: 10.1002/(sici)1097-4598(199710)20:10&lt;1236::aid-mus5&gt;3.0.co;2-d</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Van Den Bergh PYK, Van Doorn PA, Hadden RDM, et al. European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint Task Force — Second revision. J Peripher Nerv Sys. 2021;26(3):242–268. doi: 10.1111/jns.12455</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Ghoreishi Z, Keshavarz S, Asghari Jafarabadi M, et al. Risk factors for paclitaxel-induced peripheral neuropathy in patients with breast cancer. BMC Cancer. 2018;18(1):958. doi: 10.1186/s12885-018-4869-5</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Jordan B, Jahn F, Sauer S, Jordan K. Prevention and management of chemotherapy-induced polyneuropathy. Breast Care (Basel). 2019;14(2):79–84. doi: 10.1159/000499599</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Timmins HC, Mizrahi D, Li T, et al. Metabolic and lifestyle risk factors for chemotherapy-induced peripheral neuropathy in taxane and platinum-treated patients: a systematic review. J Cancer Surviv. 2023;17(1):222–236. doi: 10.1007/s11764-021-00988-x</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Morton RF, Sloan JA, Grothey A, et al. A comparison of simple single-item measures and the common toxicity criteria in detecting the onset of oxaliplatin-induced peripheral neuropathy in patients with colorectal cancer. JCO. 2005;23(16):8087. doi: 10.1200/jco.2005.23.16_suppl.8087</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Park SB, Kwok JB, Asher R, et al. Clinical and genetic predictors of paclitaxel neurotoxicity based on patient- versus clinician-reported incidence and severity of neurotoxicity in the ICON7 trial. Ann Oncol. 2017;28(11):2733–2740. doi: 10.1093/annonc/mdx491</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Burakgazi AZ, Messersmith W, Vaidya D, et al. Longitudinal assessment of oxaliplatin-induced neuropathy. Neurology. 2011;77(10):980–986. doi: 10.1212/WNL.0b013e31822cfc59</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Molassiotis A, Cheng HL, Lopez V, et al. Are we mis-estimating chemotherapy-induced peripheral neuropathy? Analysis of assessment methodologies from a prospective, multinational, longitudinal cohort study of patients receiving neurotoxic chemotherapy. BMC Cancer. 2019;19(1):132. doi: 10.1186/s12885-019-5302-4</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Холодова Н.Б., Понкратова Ю.А., Синкин М.В. Клинические и электронейромиографические особенности постхимиотерапевтической полинейропатии. Журнал неврологии и психиатрии им. С.С. Корсакова. 2017;117(9):59–66. Kholodova NB, Ponkratova YuA, Sinkin MV. Clinical and electromyography characteristics of chemotherapy-induced polyneuropathy. S.S. Korsakov Journal of Neurology and Psychiatry. 2017;117(9):59–66. doi: 10.17116/jnevro20171179159-66</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Kim SH, Kim W, Kim JH, et al. A Prospective study of chronic oxaliplatin-induced neuropathy in patients with colon cancer: long-term outcomes and predictors of severe oxaliplatin-induced neuropathy. J Clin Neurol. 2018;14(1):81–89. doi: 10.3988/jcn.2018.14.1.81</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Myftiu B, Hundozi Z, Sermaxhaj F, et al. Chemotherapy-Induced Peripheral Neuropathy (CIPN) in patients receiving 4–6 cycles of platinum-based and taxane-based chemotherapy: a prospective, single-center study from Kosovo. Med Sci Monit. 2022;28: e937856. doi: 10.12659/MSM.937856.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Mansukhani K, Dhonde M, Sreenivasan A, et al. Sural radial amplitude ratio: a study in healthy Indian subjects. Ann Indian Acad Neurol. 2020;23(3):255–260. doi: 10.4103/aian.AIAN_321_20</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Guo Y, Palmer JL, Brown XS, Fu JB. Sural and radial sensory responses in patients with sensory polyneuropathy. Clin Med Rev Case Rep. 2015;2(3):049. doi: 10.23937/2378-3656/1410049</mixed-citation></ref></ref-list></back></article>
