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  2. Keyword: Muscular Dystrophy, Duchenne / genetics
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Original Article

Behavior of Blood Pressure Variables in Children and Adolescents with Duchenne Muscular Dystrophy

Fabiane R. R. H. Marui et al. Henrique Tria Bianco Maria Teresa N. Bombig Natascha G. F. Palmeira … José M. Thalenberg Fernando Focaccia Povoa Maria Cristina de O. Izar Francisco Antonio H. Fonseca Acary S. B. de Oliveira Rui M. S. Povoa

Abstract

Background:

Duchenne muscular dystrophy is an X-chromosome-linked genetic disorder (locus Xp21). Involvement of the cardiovascular system is characterized by fibrous degeneration/replacement of myocytes with consequent ventricular hypertrophy and arterial hypertension.

Objective:

To assess, by using 24-hour ambulatory blood pressure monitoring, the behavior of blood pressure variables in children and adolescents with a confirmed diagnosis of Duchenne muscular dystrophy.

Methods:

Prospective observational cohort study, which selected 46 patients followed up on an outpatient basis, divided according to age groups. Blood pressure was classified according to the age percentile. The monitoring interpretation includes systolic and diastolic blood pressure means, systolic and diastolic blood pressure loads, and nocturnal dipping. The blood pressure means were calculated for the 24-hour, wakefulness and sleep periods. Nocturnal dipping was defined as a drop in blood pressure means during sleep greater than 10%. The significance level adopted was p < 0.05.

Results:

Nocturnal dipping for systolic blood pressure was present in 29.9% of the participants. Approximately 53% of them had attenuated nocturnal dipping, and 15%, reverse nocturnal dipping. The age groups of 9-11 years and 6-8 years had the greatest percentage of attenuation, 19.1% and 14.9%, respectively. Regarding diastolic blood pressure, nocturnal dipping was identified in 53.2% of the children, being extreme in 27.7% of those in the age group of 6-11 years.

Conclusions:

The early diagnosis of blood pressure changes can allow the appropriate and specific therapy, aimed at increasing the life expectancy of patients with Duchenne muscular dystrophy.

  • Cardiovascular Diseases / genetics
  • Child
  • Hypertension
  • Male
  • Muscular Dystrophy, Duchenne / genetics
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Creative Commons Attribution (CC BY) Creative Commons license
01/06/2018 DOI: 10.5935/abc.20180085
Figure 1
IJCS
Case Report

Heart Transplantation in Becker Muscular Dystrophy Patient: Case-Report of a 15-Year Follow-up

Marcio Madeira et al. Sara Ranchordás Tiago Nolasco Marta Marques … Maria José Rebocho José Neves

Introduction

Becker muscular dystrophy is a rare genetic disease with a birth incidence of approximately 1:30000 in males. The disease results from a X-linked recessive mutation on the gene located at Xp21, which encodes the dystrophin protein. Clinical manifestations include progressive skeletal muscle weakness and dilated cardiomyopathy which can lead to refractory heart failure. There is no correlation between the severity of cardiac manifestations and the genetic abnormalities.

[…]

  • Aftercare
  • Muscular Dystrophy, Duchenne / genetics
  • Myotonia Congenita, Heart Transplantation
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Creative Commons Attribution (CC BY) Creative Commons license
01/01/2018 DOI: 10.5935/2359-4802.20170083 Views 2

How to cite this article

EndNote RIS

Electronic Document Format (Vancouver)

Marui FRRH, Bianco HT, Bombig MTN, Palmeira NGF, Thalenberg JM, Povoa FF, Izar MCO, et al. Behavior of Blood Pressure Variables in Children and Adolescents with Duchenne Muscular Dystrophy. Arquivos Brasileiros de Cardiologia 2018;110(6):551-7.

Electronic Document Format (ABNT)

Marui, Fabiane R. R. H.; Bianco, Henrique Tria; Bombig, Maria Teresa N.; Palmeira, Natascha G. F.; Thalenberg, José M.; Povoa, Fernando Focaccia; Izar, Maria Cristina de O.; Fonseca, Francisco Antonio H.; Oliveira, Acary S. B. de; Povoa, Rui M. S.. Behavior of Blood Pressure Variables in Children and Adolescents with Duchenne Muscular Dystrophy. Arquivos Brasileiros de Cardiologia, v. 110, n. 6, p. 551-557, May. 2018.

Electronic Document Format (APA)

Marui, F. R. R. H., Bianco, H. T., Bombig, M. T. N., Palmeira, N. G. F., Thalenberg, J. M., Povoa, F. F., Izar, M. C. O., Fonseca, F. A. H., Oliveira, A. S. B. , & Povoa, R. M. S. (2018). Behavior of Blood Pressure Variables in Children and Adolescents with Duchenne Muscular Dystrophy. Arquivos Brasileiros de Cardiologia, 110(6), 551-557.

Electronic Document Format (ISO)

Marui, Fabiane R. R. H. and Bianco, Henrique Tria and Bombig, Maria Teresa N. and Palmeira, Natascha G. F. and Thalenberg, José M. and Povoa, Fernando Focaccia and Izar, Maria Cristina de O. and Fonseca, Francisco Antonio H. and Oliveira, Acary S. B. de and Povoa, Rui M. S.. Behavior of Blood Pressure Variables in Children and Adolescents with Duchenne Muscular Dystrophy. Arquivos Brasileiros de Cardiologia [online]. 2018, vol. 110, n. 6, [cited 2026-10-14], pp. 551-557. Available from: <https://journals.cardiol.br/en/article/behavior-of-blood-pressure-variables-in-children-and-adolescents-with-duchenne-muscular-dystrophy/>. ISSN 0066-782X

EndNote RIS

Electronic Document Format (Vancouver)

Madeira M, Ranchordás S, Nolasco T, Marques M, Rebocho MJ, Neves J. Heart Transplantation in Becker Muscular Dystrophy Patient: Case-Report of a 15-Year Follow-up. International Journal of Cardiovascular Sciences 2018;31(1):82-4.

Electronic Document Format (ABNT)

Madeira, Marcio; Ranchordás, Sara; Nolasco, Tiago; Marques, Marta; Rebocho, Maria José; Neves, José. Heart Transplantation in Becker Muscular Dystrophy Patient: Case-Report of a 15-Year Follow-up. International Journal of Cardiovascular Sciences, v. 31, n. 1, p. 82-84, Dec. 2017.

Electronic Document Format (APA)

Madeira, M., Ranchordás, S., Nolasco, T., Marques, M., Rebocho, M. J., & Neves, J. (2018). Heart Transplantation in Becker Muscular Dystrophy Patient: Case-Report of a 15-Year Follow-up. International Journal of Cardiovascular Sciences, 31(1), 82-84.

Electronic Document Format (ISO)

Madeira, Marcio and Ranchordás, Sara and Nolasco, Tiago and Marques, Marta and Rebocho, Maria José and Neves, José. Heart Transplantation in Becker Muscular Dystrophy Patient: Case-Report of a 15-Year Follow-up. International Journal of Cardiovascular Sciences [online]. 2018, vol. 31, n. 1, [cited 2026-10-14], pp. 82-84. Available from: <https://journals.cardiol.br/en/article/heart-transplantation-in-becker-muscular-dystrophy-patient-case-report-of-a-15-year-follow-up/>. ISSN 2359-4802

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