Int J Angiol 2019; 28(04): 245-248
DOI: 10.1055/s-0039-1688983
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Head-Up Tilt Test in Risk Stratification of Patients with Hypertrophic Cardiomyopathy

Hana Sediva
1   Department of Cardiology, 2nd Faculty of Medicine and Motol University Hospital, Prague, Czech Republic
,
T. Hnat
1   Department of Cardiology, 2nd Faculty of Medicine and Motol University Hospital, Prague, Czech Republic
,
J. Bonaventura
1   Department of Cardiology, 2nd Faculty of Medicine and Motol University Hospital, Prague, Czech Republic
,
J. Slesarenko
1   Department of Cardiology, 2nd Faculty of Medicine and Motol University Hospital, Prague, Czech Republic
,
J. Veselka
1   Department of Cardiology, 2nd Faculty of Medicine and Motol University Hospital, Prague, Czech Republic
› Author Affiliations
Further Information

Publication History

Publication Date:
16 June 2019 (online)

Abstract

Conflicting results have been published considering the role of head-up tilt test (HUTT) positivity as a prognostic factor in patients with hypertrophic cardiomyopathy (HCM). The relationship between HCM patients' genotype and their HUTT results has not been previously reported.

The aim of this study was to evaluate patients with HCM and their HUTT results in regard to its value for outcome prediction and to investigate the relation of patients' genotype and their HUTT results.

Seventy-four (51 ± 15 years; 42% women; median follow-up 72 months) HCM patients were divided into two groups based on their HUTT results and were retrospectively analyzed. In 67 (90.5%) subjects included in the analysis, next-generation sequencing-based genomic testing was performed. A composite end point of unexplained syncope, heart failure hospitalization, and death was defined.

A total of 14 patients (18.9%) had positive HUTT (HUTT+), whereas 60 (81.1%) had negative HUTT (HUTT–). Except for the New York Heart Association functional class (p = 0.01), both groups had similar characteristics. Positive genotype was evenly distributed between the two groups. Composite end point occurred in 5 patients (35.7%) in HUTT+ group versus 14 (23.3%) patients in HUTT– group (p = 0.33).

We did not find a relationship between HUTT results and long-term outcome. We found no association between HUTT results and genotype.

 
  • References

  • 1 Buja G, Melacini P, Folino A, Miorelli M, Nava A. Spontaneous and induced vasodepressor/vasovagal syncope in hypertrophic cardiomyopathy. Clin Cardiol 1992; 15 (05) 387-389
  • 2 Sutton R, Brignole M. Twenty-eight years of research permit reinterpretation of tilt-testing: hypotensive susceptibility rather than diagnosis. Eur Heart J 2014; 35 (33) 2211-2212
  • 3 Sneddon JF, Slade A, Seo H, Camm AJ, McKenna WJ. Assessment of the diagnostic value of head-up tilt testing in the evaluation of syncope in hypertrophic cardiomyopathy. Am J Cardiol 1994; 73 (08) 601-604
  • 4 Manganelli F, Betocchi S, Ciampi Q. , et al. Comparison of hemodynamic adaptation to orthostatic stress in patients with hypertrophic cardiomyopathy with or without syncope and in vasovagal syncope. Am J Cardiol 2002; 89 (12) 1405-1410
  • 5 Forleo C, Guida P, Iacoviello M. , et al. Head-up tilt testing for diagnosing vasovagal syncope: a meta-analysis. Int J Cardiol 2013; 168 (01) 27-35
  • 6 Elliott PM, Poloniecki J, Dickie S. , et al. Sudden death in hypertrophic cardiomyopathy: identification of high risk patients. J Am Coll Cardiol 2000; 36 (07) 2212-2218
  • 7 Spirito P, Autore C, Rapezzi C. , et al. Syncope and risk of sudden death in hypertrophic cardiomyopathy. Circulation 2009; 119 (13) 1703-1710
  • 8 Elliott PM, Anastasakis A, Borger MA. , et al; Authors/Task Force members. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the task force for the diagnosis and management of hypertrophic cardiomyopathy of the European Society of Cardiology (ESC). Eur Heart J 2014; 35 (39) 2733-2779
  • 9 Gersh BJ, Maron BJ, Bonow RO. , et al; American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines; American Association for Thoracic Surgery; American Society of Echocardiography; American Society of Nuclear Cardiology; Heart Failure Society of America; Heart Rhythm Society; Society for Cardiovascular Angiography and Interventions; Society of Thoracic Surgeons. 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: a report of the American College of Cardiology Foundation/American Heart Association task force on practice guidelines. Circulation 2011; 124 (24) e783-e831
  • 10 Veselka J, Anavekar NS, Charron P. Hypertrophic obstructive cardiomyopathy. Lancet 2017; 389 (10075): 1253-1267
  • 11 Cooper RM, Raphael CE, Liebregts M, Anavekar NS, Veselka J. New developments in hypertrophic cardiomyopathy. Can J Cardiol 2017; 33 (10) 1254-1265
  • 12 Richards S, Aziz N, Bale S. , et al; ACMG Laboratory Quality Assurance Committee. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015; 17 (05) 405-424
  • 13 Bonaventura J, Norambuena P, Tomasov P. , et al. The utility of the Mayo Score for predicting the yield of genetic testing in patients with hypertrophic cardiomyopathy. Arch Med Sci 2019; 15 (03) 641-649
  • 14 Dimitrow PP, Chojnowska L, Rudzinski T. , et al. Sudden death in hypertrophic cardiomyopathy: old risk factors re-assessed in a new model of maximalized follow-up. Eur Heart J 2010; 31 (24) 3084-3093
  • 15 Gilligan DM, Nihoyannopoulos P, Chan WL, Oakley CM. Investigation of a hemodynamic basis for syncope in hypertrophic cardiomyopathy. Use of a head-up tilt test. Circulation 1992; 85 (06) 2140-2148
  • 16 Thomson HL, Morris-Thurgood J, Atherton J, Frenneaux M. Reduced cardiopulmonary baroreflex sensitivity in patients with hypertrophic cardiomyopathy. J Am Coll Cardiol 1998; 31 (06) 1377-1382
  • 17 Williams L, Frenneaux M. Syncope in hypertrophic cardiomyopathy: mechanisms and consequences for treatment. Europace 2007; 9 (09) 817-822
  • 18 Brignole M, Moya A, de Lange FJ. , et al; ESC Scientific Document Group. 2018 ESC guidelines for the diagnosis and management of syncope. Eur Heart J 2018; 39 (21) 1883-1948
  • 19 Thaman R, Elliott PM, Shah JS. , et al. Reversal of inappropriate peripheral vascular responses in hypertrophic cardiomyopathy. J Am Coll Cardiol 2005; 46 (05) 883-892
  • 20 Sadoul N, Prasad K, Elliott PM, Bannerjee S, Frenneaux MP, McKenna WJ. Prospective prognostic assessment of blood pressure response during exercise in patients with hypertrophic cardiomyopathy. Circulation 1997; 96 (09) 2987-2991
  • 21 Thomson HL, Morris-Thurgood J, Atherton J, McKenna WJ, Frenneaux MP. Reflex responses of venous capacitance vessels in patients with hypertrophic cardiomyopathy. Clin Sci (Lond) 1998; 94 (04) 339-346
  • 22 Ungar A, Sgobino P, Russo V. , et al; International Study on Syncope of Uncertain Etiology 3 (ISSUE-3) Investigators. Diagnosis of neurally mediated syncope at initial evaluation and with tilt table testing compared with that revealed by prolonged ECG monitoring. An analysis from the Third International Study on Syncope of Uncertain Etiology (ISSUE-3). Heart 2013; 99 (24) 1825-1831
  • 23 Macatrão-Costa MF, Arteaga-Fernandez E, de Brito FS. , et al. Evaluation of the autonomic function in patients with hypertrophic cardiomyopathy with and without syncope. Arq Bras Cardiol 2013; 100 (02) 180-186