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Within-visit SBP variability from childhood to adulthood and markers of cardiovascular end-organ damage in mid-life.
Meng, Yaxing; Magnussen, Costan G; Wu, Feitong; Buscot, Marie-Jeanne; Juonala, Markus; Pahkala, Katja; Hutri-Kähönen, Nina; Kähönen, Mika; Laitinen, Tomi; Viikari, Jorma S A; Raitakari, Olli T; Sharman, James E.
Afiliación
  • Meng Y; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Magnussen CG; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Wu F; Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku.
  • Buscot MJ; Centre for Population Health Research, University of Turku and Turku University Hospital.
  • Juonala M; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Pahkala K; Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia.
  • Hutri-Kähönen N; Department of Medicine, University of Turku.
  • Kähönen M; Division of Medicine, Turku University Hospital.
  • Laitinen T; Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku.
  • Viikari JSA; Centre for Population Health Research, University of Turku and Turku University Hospital.
  • Raitakari OT; Paavo Nurmi Centre, Sports & Exercise Medicine Unit, Department of Physical Activity and Health, University of Turku, Turku.
  • Sharman JE; Department of Pediatrics, Tampere University and Tampere University Hospital.
J Hypertens ; 39(9): 1865-1875, 2021 09 01.
Article en En | MEDLINE | ID: mdl-34397629
ABSTRACT

BACKGROUND:

Within-visit SBP variability is associated with age and SBP, but its long-term clinical significance is unknown. We examined the association between child, adult, and life-time within-visit SBP variability with markers of end-organ damage using data from a 31-year longitudinal study.

METHODS:

Within-visit SBP variability was calculated as the standard deviation of three sitting SBP readings among up to 3010 participants aged 6-18 years (childhood) who were re-measured up to seven times to mid-adulthood. Markers of cardiovascular end-organ damage in adulthood were carotid intima--media thickness, brachial flow-mediated dilatation, carotid distensibility, pulse wave velocity, left ventricular mass index, carotid plaque, and coronary artery calcification.

RESULTS:

The mean (standard deviation) cumulative within-visit SBP variability was 2.7 (1.5) mmHg in childhood, 3.9 (1.9) mmHg in adulthood and 3.7 (1.5) mmHg across the observed life-time. Childhood within-visit SBP variability was not correlated with its subsequent values measured from 3 to 31 years later. With adjustment for age, sex, cumulative SBP, BMI and serum lipids, neither child, adult, or life-time cumulative within-visit SBP variability associated with markers of cardiovascular end-organ damage. However, higher child, adult, and life-time cumulative SBP significantly associated with higher carotid intima--media thickness, higher pulse wave velocity, lower brachial flow-mediated dilatation, lower carotid distensibility in adulthood.

CONCLUSION:

Within-visit SBP variability from childhood to adulthood does not provide additional predictive utility over SBP over the same period of the life course.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Grosor Intima-Media Carotídeo / Análisis de la Onda del Pulso Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Hypertens Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Grosor Intima-Media Carotídeo / Análisis de la Onda del Pulso Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Hypertens Año: 2021 Tipo del documento: Article