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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">ijcs</journal-id>
      <journal-title-group>
        <journal-title>International Journal of Cardiovascular Sciences</journal-title>
        <abbrev-journal-title abbrev-type="publisher">Int J Cardiovasc Sci </abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2359-4802</issn>
      <issn pub-type="epub">2359-5647</issn>
      <publisher>
        <publisher-name>Sociedade Brasileira de Cardiologia</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">JrkMBgJY8P9xGLjvFcSVdjd</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S2359-56472020000400357</article-id>
      <article-id pub-id-type="publisher-id">ijcs.20200132</article-id>
      <article-id pub-id-type="doi">10.36660/ijcs.20200132</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>EDITORIAL</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Vascular Aging and Arterial Stiffness in Older Adults</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-6352-3330</contrib-id>
          <name>
            <surname>Campana</surname>
            <given-names>Erika Maria Gon&#231;alves</given-names>
          </name>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
          <xref ref-type="aff" rid="aff2">
            <sup>2</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-5784-9991</contrib-id>
          <name>
            <surname>Inuzuka</surname>
            <given-names>Sayuri</given-names>
          </name>
          <xref ref-type="aff" rid="aff2">
            <sup>2</sup>
          </xref>
          <xref ref-type="aff" rid="aff3">
            <sup>3</sup>
          </xref>
        </contrib>
      </contrib-group>
      <aff id="aff1">
        <label>1</label>
        <institution content-type="orgname">Universidade do Estado do Rio de Janeiro</institution>
        <addr-line>
          <named-content content-type="city">Rio de Janeiro</named-content>
          <named-content content-type="state">RJ</named-content>
        </addr-line>
        <country country="BR">Brazil</country>
        <institution content-type="original">Universidade do Estado do Rio de Janeiro (UERJ), Rio de Janeiro, RJ &#8211; Brazil.</institution>
      </aff>
      <aff id="aff2">
        <label>2</label>
        <institution content-type="orgname">Universidade de Nova Igua&#231;u</institution>
        <addr-line>
          <named-content content-type="city">Rio de Janeiro</named-content>
          <named-content content-type="state">RJ</named-content>
        </addr-line>
        <country country="BR">Brazil</country>
        <institution content-type="original">Universidade de Nova Igua&#231;u, Rio de Janeiro, RJ &#8211; Brazil.</institution>
      </aff>
      <aff id="aff3">
        <label>3</label>
        <institution content-type="orgname">Universidade Federal de Goi&#225;s</institution>
        <addr-line>
          <named-content content-type="city">Goi&#225;s</named-content>
          <named-content content-type="state">GO</named-content>
        </addr-line>
        <country country="BR">Brazil</country>
        <institution content-type="original">Universidade Federal de Goi&#225;s (UFG), Goi&#225;s, GO &#8211; Brazil.</institution>
      </aff>
      <author-notes>
        <corresp id="c01"><bold>Mailing Address: Erika Maria Gon&#231;alves Campana</bold> Rua S&#227;o Janu&#225;rio, 159 / 1103 B. Postal Code: 24130386, Fonseca - Niter&#243;i, RJ - Brazil. E-mail: <email>erikamaria@cardiol.br</email> , <email>campanaemg@predialnet.com.br</email>
				</corresp>
      </author-notes>
      <pub-date date-type="pub" publication-format="electronic">
        <day>31</day>
        <month>07</month>
        <year>2020</year>
      </pub-date>
      <pub-date date-type="collection" publication-format="electronic">
        <season>Jul-Aug</season>
        <year>2020</year>
      </pub-date>
      <volume>33</volume>
      <issue>4</issue>
      <fpage>357</fpage>
      <lpage>359</lpage>
      <permissions>
        <license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/" xml:lang="en">
          <license-p> This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. </license-p>
        </license>
      </permissions>
      <kwd-group xml:lang="en">
        <kwd>Cardiovascular Diseases/mortality</kwd>
        <kwd>Hypertension</kwd>
        <kwd>Vascular stiffness</kwd>
        <kwd>Risk factors</kwd>
        <kwd>Biomarkers</kwd>
        <kwd>Blood Pressure</kwd>
        <kwd>Aged</kwd>
        <kwd>Frailty</kwd>
        <kwd>Pulse Wave Analyses</kwd>
      </kwd-group>
      <counts>
        <fig-count count="2"/>
        <table-count count="0"/>
        <equation-count count="0"/>
        <ref-count count="9"/>
        <page-count count="3"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <p>Deaths from cardiovascular disease, according to the WHO, are projected to reach around 14 million by 2030. The global population is aging at an accelerated rate and the prevalence of arterial hypertension (AH) increases with advancing age.<sup><xref ref-type="bibr" rid="B1">1</xref></sup> Aging is the common denominator in several cardiovascular diseases. Arterial stiffness and increased pulse wave velocity (PWV), as well as central systolic pressure are major predictors of cardiovascular events. ( <xref ref-type="fig" rid="f01">Figure 1</xref> ) <sup><xref ref-type="bibr" rid="B2">2</xref></sup></p>
    <p>
      <fig id="f01">
        <label>Figure 1</label>
        <caption>
          <title>&#8211; Ideal lifecourse and vascular aging (Adapted from Nilsson et al Early Vascular Aging and Prevention)[2] CV: cardiovascular; TOD: target organ damage; BP: blood pressure.</title>
        </caption>
        <graphic xlink:href="2359-5647-ijcs-33-04-0357-00132-gf01.jpg"/></fig>
    </p>
    <p>Arterial stiffness reflects the true arterial wall damage of risk factors, and it increases with aging. On the other hand, mean blood pressure (MBP), glycemia and lipids are circulating markers whose values fluctuate along the follow-up of patients. Thus, measuring circulating biomarkers at a certain time may give only a snapshot and not the whole history of arterial wall damage. As shown in <xref ref-type="fig" rid="f02">Figure 2</xref> , the gray zone before the time at measurement, when the risk assessment of a hypothetical patient is done, represents a period of life when circulating biomarkers may present altered values and, consequently, aggression to the vascular wall, interchanged with periods of good control of circulating biomarkers. This indicates that, most often, the physician does not know the amount of exposure to CV risk factors that a patient presents throughout life. Because risk scores perform a cross-sectional analysis of a single moment, they may not be able to quantify the overall cardiovascular and residual risks of each patient. However, the evaluation of arterial stiffness expresses the sum of all the aggressions caused by circulating markers on the arterial wall over time and, for this reason, it expresses more accurately the future risk of a CV event or death.<sup><xref ref-type="bibr" rid="B2">2</xref></sup> ( <xref ref-type="fig" rid="f02">Figure 2</xref> )</p>
    <p>
      <fig id="f02">
        <label>Figure 2</label>
        <caption>
          <title>&#8211; Vascular Aging (Adapted from Nilsson et al Early Vascular Aging and Prevention). Mean BP (MBP); Cardiovascular (CV) events[2].</title>
        </caption>
        <graphic xlink:href="2359-5647-ijcs-33-04-0357-00132-gf02.jpg"/></fig>
    </p>
    <p>Further assessment and stratification of risk, in addition to the biomarkers already established, such as blood pressure (BP), blood glucose, cholesterol and carotid intima-media thickness, must provide a better and cost-effective risk prediction. Therefore, a study investigated whether a 1 m/s increase in PWV was associated with a 7% increased risk of a cardiovascular event for a 60 year old man.<sup><xref ref-type="bibr" rid="B3">3</xref></sup></p>
    <p>In addition, the altered behavior of central hemodynamic parameters, such as central systolic blood pressure (cSBP) and the (heart rate-corrected) augmentation index (AI), is influenced by arterial stiffness and plays a crucial role in the interface between the traditional cardiovascular continuum vascular and aging continuum, which represents the current view of the pathophysiology of cardiovascular diseases.<sup><xref ref-type="bibr" rid="B4">4</xref> - <xref ref-type="bibr" rid="B6">6</xref></sup></p>
    <p>In addition to cardiovascular impairment, another concern related to aging is cognition. A review showed that arterial stiffness severity was positively correlated with cognitive impairment. The mechanisms may be associated with greater arterial pulsatility, damaging the cerebral microcirculation, which causes various phenomena associated with cerebral small vessel diseases. It may also be associated with reductions in white matter and gray matter integrity, medial temporal lobe atrophy and A&#946; protein deposition.<sup><xref ref-type="bibr" rid="B7">7</xref></sup></p>
    <p>Emerging evidence suggests that frailty is a risk factor for CVD. Individuals are considered frail if they present at least three out of these five items: unintentional weight loss of &#8805;10 lbs within a year, self-reported exhaustion, weakness as measured by grip strength, slow walking speed, and decreased physical activity. High frailty levels are associated with increased stiffness.<sup><xref ref-type="bibr" rid="B8">8</xref></sup></p>
    <p>The article published in this issue was a cross-sectional, observational study of participants enrolled in the AGA@4life project, developed to evaluate the effects of several interventions (psychological, physical and nutritional therapy). The aim of the preliminary analysis was to identify the main determinants of arterial stiffness in the very old, identifying the factors that may accelerate arterial ageing and potential routes for preventive actions targeting the maintenance of vascular health. The study enrolled 54 elderly aged between 65 and 94 years from a day care center, in Vilarinho, Portugal.<sup><xref ref-type="bibr" rid="B9">9</xref></sup></p>
    <p>Arterial stiffness was obtained by an oscillometric method that uses the Mobil-O-Graph, a method validated in previous studies. Hypertension was observed in the large majority of the participants (80%) which, in its isolated form, is an important cardiovascular risk factor; however, only 64% were under treatment. Aging was seen as a determinant factor for PWV and blood pressure, and there was an intrinsic relationship between PWV and blood pressure. The study also showed an association between PWV and renal function, as well as frailty.</p>
    <p>Most of the knowledge on accelerated vascular aging has been acquired from the general population, not including the most advanced age group. Therefore, researches on arterial stiffness in the elderly, such as the one carried out by the AGA@4life project,<sup><xref ref-type="bibr" rid="B9">9</xref></sup> are important to develop adequate and useful intervention programs for a better cardiovascular protection of this group.</p>
  </body>
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    <fn-group>
      <fn fn-type="other">
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</article>
