Abstract
Background and purpose
Takotsubo cardiomyopathy (TCM) is a serious autonomic complication of Guillain–Barré syndrome (GBS). However, the association between TCM and GBS has not been investigated in detail. We investigated the characteristics of GBS patients with TCM (GBS-TCM).
Methods
Clinical features and anti-ganglioside antibody between the GBS-TCM patients and 62 classical GBS patients without TCM as control patients were compared.
Results
Eight GBS-TCM patients were identified, in whom TCM was diagnosed at a mean of 6.5 [range 3–42] days after the onset of GBS. The age at onset of GBS was elder in the GBS-TCM patients than in the control GBS patients (76.5 [56–87] vs. 52 [20–88] years, p < 0.01). Notably, cranial nerve deficits, particularly in the lower cranial nerves, were observed in all GBS-TCM patients (100% vs. 41.9%, p < 0.01). Additionally, the GBS-TCM patients showed a higher GBS disability score at nadir (5 [4–5] vs. 4 [1–5], p < 0.01), and lower Medical Research Council sum scores at admission and nadir (37 [30–44] vs. 48 [12–60] at admission, p < 0.05, and 20 [12–44] vs. 40 [0–60] at nadir, p < 0.05, respectively). Mechanical ventilation was more frequently required in the GBS-TCM patients (62.5% vs. 11.3%, p < 0.01). Three GBS-TCM patients were positive for anti-ganglioside antibodies.
Conclusions
TCM occurred at a relatively early phase of GBS. The characteristics of GBS-TCM were the elder, lower cranial nerve involvements, severe limb weakness, and respiratory failure.
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Data availability
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
References
Leonhard SE, Mandarakas MR, Gondim FAA et al (2019) Diagnosis and management of Guillain-Barré syndrome in ten steps. Nat Rev Neurol 15(11):671–683. https://doi.org/10.1038/s41582-019-0250-9
van den Berg B, Walgaard C, Drenthen J, Fokke C, Jacobs BC, van Doorn PA (2014) Guillain-Barré syndrome: pathogenesis, diagnosis, treatment and prognosis. Nat Rev Neurol 10(8):469–482. https://doi.org/10.1038/nrneurol.2014.121
Fokke C, van den Berg B, Drenthen J, Walgaard C, van Doorn PA, Jacobs BC (2014) Diagnosis of Guillain-Barré syndrome and validation of Brighton criteria. Brain 137(Pt 1):33–43. https://doi.org/10.1093/brain/awt285
Kusunoki S, Willison HJ, Jacobs BC (2021) Antiglycolipid antibodies in Guillain-Barré and Fisher syndromes: discovery, current status and future perspective. J Neurol Neurosurg Psychiatry 92(3):311–318. https://doi.org/10.1136/jnnp-2020-325053
Sejvar JJ, Kohl KS, Gidudu J et al (2011) Guillain-Barré syndrome and Fisher syndrome: case definitions and guidelines for collection, analysis, and presentation of immunization safety data. Vaccine 29(3):599–612. https://doi.org/10.1016/j.vaccine.2010.06.003
Prasad A, Lerman A, Rihal CS (2008) Apical ballooning syndrome (Tako-Tsubo or stress cardiomyopathy): a mimic of acute myocardial infarction. Am Heart J 155(3):408–417. https://doi.org/10.1016/j.ahj.2007.11.008
Lyon AR, Bossone E, Schneider B et al (2016) Current state of knowledge on Takotsubo syndrome: a Position Statement from the Taskforce on Takotsubo Syndrome of the Heart Failure Association of the European Society of Cardiology. Eur J Heart Fail 18(1):8–27. https://doi.org/10.1002/ejhf.424
Templin C, Ghadri JR, Diekmann J et al (2015) Clinical features and outcomes of Takotsubo (stress) cardiomyopathy. N Engl J Med 373(10):929–938. https://doi.org/10.1056/NEJMoa1406761
Palazzuoli A, Lenzi C, Iovine F, Carrera A, Nuti R (2006) A case of acute heart failure associated with Guillain-Barré syndrome. Neurol Sci 26(6):447–450. https://doi.org/10.1007/s10072-006-0531-0
Ghadri JR, Wittstein IS, Prasad A et al (2018) International expert consensus document on Takotsubo syndrome (part I): Clinical characteristics, diagnostic criteria, and pathophysiology. Eur Heart J 39(22):2032–2046. https://doi.org/10.1093/eurheartj/ehy076
Ho TW, Mishu B, Li CY et al (1995) Guillain-Barré syndrome in northern China. Relationship to Campylobacter jejuni infection and anti-glycolipid antibodies. Brain. 118(3):597–605. https://doi.org/10.1093/brain/118.3.597
Kusunoki S, Chiba A, Kon K et al (1994) N-acetylgalactosaminyl GD1a is a target molecule for serum antibody in Guillain-Barré syndrome. Ann Neurol 35(5):570–576. https://doi.org/10.1002/ana.410350510
Ahmad J, Kham AS, Siddiqui MA (1985) Estimation of plasma and urinary catecholamines in Guillain-Barré syndrome. Jpn J Med 24(1):24–29. https://doi.org/10.2169/internalmedicine1962.24.24
Wittstein IS, Thiemann DR, Lima JA et al (2005) Neurohumoral features of myocardial stunning due to sudden emotional stress. N Engl J Med 352(6):539–548. https://doi.org/10.1056/NEJMoa043046
Fagius J, Wallin BG (1983) Microneurographic evidence of excessive sympathetic outflow in the Guillain-Barré syndrome. Brain 106(Pt 3):589–600. https://doi.org/10.1093/brain/106.3.589
Asahina M, Kuwabara S, Suzuki A, Hattori T (2002) Autonomic function in demyelinating and axonal subtypes of Guillain-Barré syndrome. Acta Neurol Scand 105(1):44–50. https://doi.org/10.1034/j.1600-0404.2002.00099.x
Kuzumoto Y, Shioyama M, Kihara M, Kusunoki S (2006) Abnormal sudomotor axon reflex and antiganglioside antibodies. Muscle Nerve 33(6):828–829. https://doi.org/10.1002/mus.20538
Ziemssen T, Siepmann T (2019) The investigation of the cardiovascular and sudomotor autonomic nervous system–a review. Front Neurol 10:53. https://doi.org/10.3389/fneur.2019.00053
Kanda T, Hayashi H, Tanabe H, Tsubaki T, Oda M (1989) A fulminant case of Guillain-Barré syndrome: topographic and fibre size related analysis of demyelinating changes. J Neurol Neurosurg Psychiatry 52(7):857–864. https://doi.org/10.1136/jnnp.52.7.857
van Koningsveld R, Schmitz PI, Meché FG, Visser LH, Meulstee J, van Doorn PA, Dutch GBS study group (2004) Effect of methylprednisolone when added to standard treatment with intravenous immunoglobulin for Guillain-Barré syndrome: randomised trial. Lancet. 363(9404):192–196. https://doi.org/10.1016/s0140-6736(03)15324-x
Yamagishi Y, Suzuki H, Sonoo M et al (2017) Markers for Guillain-Barré syndrome with poor prognosis: a multi-center study. J Peripher Nerv Syst 22(4):433–439. https://doi.org/10.1111/jns.12234
Acknowledgements
The authors also thank Rie Tanaka and Yukiko Watanabe for technical assistance. We thank Popiel Helena Akiko for English langage editing.
Funding
This work was supported by JSPS KAKENHI (20K07894 to M. Kuwahara).
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Conceptualization: AT and MK; data curation: AT, KY, YY, MS, SY, KO, TN, CT, JI, MK, TT, SD, KD, AI, YB, and SY; formal analysis: AT, MK, KY, and SK; funding acquisition: MK; writing the original draft: AT and MK; writing editing: SK, and YN; supervision: MK, SK, and YN.
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Financial intersts: M. Kuwahara has served as a honoraria speaker for CSL Behring, Japan Blood Product Organization, and Takeda Pharmaceuticals. S. Kusunoki received speech honoraria from Takeda, Japan Blood Product Organization, and CSL Behring and served on the DSMB for Argenx and received consulting fees as a medical expert from KM Biologics. Non-financial intersts: none.
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This study conformed with the World Medical Association Declaration of Helsinki and was approved by the Internal Review Board of Kindai University Faculty of Medicine.
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Terayama, A., Kuwahara, M., Yoshikawa, K. et al. Takotsubo cardiomyopathy in Guillain–Barré syndrome. J Neurol (2024). https://doi.org/10.1007/s00415-024-12295-3
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DOI: https://doi.org/10.1007/s00415-024-12295-3