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Within-visit SBP variability from childhood to adulthood and markers of cardiovascular end-organ damage in mid-life

Buscot Marie Jeanne; Hutri-Kähönen Nina; Juonala Markus; Kähönen Mika; Laitinen Tomi; Magnussen Costan G; Meng Yaxing; Pahkala Katja; Raitakari Olli T; Sharman James E; Viikari Jorma SA; Wu Feitong

Within-visit SBP variability from childhood to adulthood and markers of cardiovascular end-organ damage in mid-life

Buscot Marie Jeanne
Hutri-Kähönen Nina
Juonala Markus
Kähönen Mika
Laitinen Tomi
Magnussen Costan G
Meng Yaxing
Pahkala Katja
Raitakari Olli T
Sharman James E
Viikari Jorma SA
Wu Feitong
Katso/Avaa
12m embargo (1.003Mb)
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LIPPINCOTT WILLIAMS & WILKINS
doi:10.1097/HJH.0000000000002855
URI
http://www.doi.org/10.1097/HJH.0000000000002855
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021102752651
Tiivistelmä

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.

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  • Rinnakkaistallenteet [19207]

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