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  1. Article ; Online: Early cardiovascular structural and functional abnormalities as a guide to future morbid events.

    Koskinen, Juhani S / Raitakari, Olli T

    European journal of preventive cardiology

    2021  Volume 28, Issue 15, Page(s) e1–e2

    MeSH term(s) Humans ; Cardiovascular Diseases ; Morbidity ; Cardiovascular System
    Language English
    Publishing date 2021-02-16
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 2626011-6
    ISSN 2047-4881 ; 2047-4873
    ISSN (online) 2047-4881
    ISSN 2047-4873
    DOI 10.1177/2047487320908700
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Subclinical atherosclerosis in young adults predicting cardiovascular disease: The Cardiovascular Risk in Young Finns Study.

    Raitakari, Olli T / Magnussen, Costan G / Juonala, Markus / Kartiosuo, Noora / Pahkala, Katja / Rovio, Suvi / Koskinen, Juhani S / Mykkänen, Juha / Laitinen, Tomi P / Kähönen, Mika / Nuotio, Joel / Viikari, Jorma S A

    Atherosclerosis

    2024  , Page(s) 117515

    Abstract: Background and aims: Atherosclerosis is accompanied by pre-clinical vascular changes that can be detected using ultrasound imaging. We examined the value of such pre-clinical features in identifying young adults who are at risk of developing ... ...

    Abstract Background and aims: Atherosclerosis is accompanied by pre-clinical vascular changes that can be detected using ultrasound imaging. We examined the value of such pre-clinical features in identifying young adults who are at risk of developing atherosclerotic cardiovascular disease (ASCVD).
    Methods: A total of 2641 individuals free of ASCVD were examined at the mean age of 32 years (range 24-45 years) for carotid artery intima-media thickness (IMT) and carotid plaques, carotid artery elasticity, and brachial artery flow-mediated endothelium-dependent vasodilation (FMD). The average follow-up time to event/censoring was 16 years (range 1-17 years).
    Results: Sixty-seven individuals developed ASCVD (incidence 2.5%). The lowest incidence (1.1%) was observed among those who were estimated of having low risk according to the SCORE2 risk algorithm (<2.5% 10-year risk) and who did not have plaque or high IMT (upper decile). The highest incidence (11.0%) was among those who were estimated of having a high risk (≥2.5% 10-year risk) and had positive ultrasound scan for carotid plaque and/or high IMT (upper decile). Carotid plaque and high IMT remained independently associated with higher risk in multivariate models. The distributions of carotid elasticity indices and brachial FMD did not differ between cases and non-cases.
    Conclusions: Screening for carotid plaque and high IMT in young adults may help identify individuals at high risk for future ASCVD.
    Language English
    Publishing date 2024-03-19
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 80061-2
    ISSN 1879-1484 ; 0021-9150
    ISSN (online) 1879-1484
    ISSN 0021-9150
    DOI 10.1016/j.atherosclerosis.2024.117515
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Childhood Dyslipidemia and Carotid Atherosclerotic Plaque in Adulthood: The Cardiovascular Risk in Young Finns Study.

    Koskinen, Juhani S / Kytö, Ville / Juonala, Markus / Viikari, Jorma S A / Nevalainen, Jaakko / Kähönen, Mika / Lehtimäki, Terho / Hutri-Kähönen, Nina / Laitinen, Tomi P / Tossavainen, Päivi / Jokinen, Eero / Magnussen, Costan G / Raitakari, Olli T

    Journal of the American Heart Association

    2023  Volume 12, Issue 7, Page(s) e027586

    Abstract: Background Childhood exposure to dyslipidemia is associated with adult atherosclerosis, but it is unclear whether the long-term risk associated with dyslipidemia is attenuated on its resolution by adulthood. We aimed to address this question by examining ...

    Abstract Background Childhood exposure to dyslipidemia is associated with adult atherosclerosis, but it is unclear whether the long-term risk associated with dyslipidemia is attenuated on its resolution by adulthood. We aimed to address this question by examining the links between childhood and adult dyslipidemia on carotid atherosclerotic plaques in adulthood. Methods and Results The Cardiovascular Risk in Young Finns Study is a prospective follow-up of children that began in 1980. Since then, follow-up studies have been conducted regularly. In 2001 and 2007, carotid ultrasounds were performed on 2643 participants at the mean age of 36 years to identify carotid plaques and plaque areas. For childhood lipids, we exploited several risk factor measurements to determine the individual cumulative burden for each lipid during childhood. Participants were categorized into the following 4 groups based on their childhood and adult dyslipidemia status: no dyslipidemia (reference), incident, resolved, and persistent. Among individuals with carotid plaque, linear regression models were used to study the association of serum lipids with plaque area. The prevalence of plaque was 3.3% (N=88). In models adjusted for age, sex, and nonlipid cardiovascular risk factors, the relative risk for carotid plaque was 2.34 (95% CI, 0.91-6.00) for incident adult dyslipidemia, 3.00 (95% CI, 1.42-6.34) for dyslipidemia resolved by adulthood, and 5.23 (95% CI, 2.57-10.66) for persistent dyslipidemia. Carotid plaque area correlated with childhood total, low-density lipoprotein, and non-high-density lipoprotein cholesterol levels. Conclusions Childhood dyslipidemia, even if resolved by adulthood, is a risk factor for adult carotid plaque. Furthermore, among individuals with carotid plaque, childhood lipids associate with plaque size. These findings highlight the importance of primordial prevention of dyslipidemia in childhood to reduce atherosclerosis development.
    MeSH term(s) Child ; Adult ; Humans ; Plaque, Atherosclerotic/complications ; Risk Factors ; Prospective Studies ; Finland/epidemiology ; Cardiovascular Diseases/epidemiology ; Atherosclerosis/epidemiology ; Heart Disease Risk Factors ; Cholesterol ; Carotid Artery Diseases/diagnostic imaging ; Carotid Artery Diseases/epidemiology ; Carotid Artery Diseases/etiology
    Chemical Substances Cholesterol (97C5T2UQ7J)
    Language English
    Publishing date 2023-03-16
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2653953-6
    ISSN 2047-9980 ; 2047-9980
    ISSN (online) 2047-9980
    ISSN 2047-9980
    DOI 10.1161/JAHA.122.027586
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Blood Pressure at Different Life Stages Over the Early Life Course and Intima-Media Thickness.

    Meng, Yaxing / Sharman, James E / Koskinen, Juhani S / Juonala, Markus / Viikari, Jorma S A / Buscot, Marie-Jeanne / Wu, Feitong / Fraser, Brooklyn J / Rovio, Suvi P / Kähönen, Mika / Rönnemaa, Tapani / Jula, Antti / Niinikoski, Harri / Raitakari, Olli T / Pahkala, Katja / Magnussen, Costan G

    JAMA pediatrics

    2023  Volume 178, Issue 2, Page(s) 133–141

    Abstract: Importance: Although cardiovascular disease (CVD) begins in early life, the extent to which blood pressure (BP) at different life stages contributes to CVD is unclear.: Objective: To determine the relative contribution of BP at different life stages ... ...

    Abstract Importance: Although cardiovascular disease (CVD) begins in early life, the extent to which blood pressure (BP) at different life stages contributes to CVD is unclear.
    Objective: To determine the relative contribution of BP at different life stages across the early-life course from infancy to young adulthood with carotid intima-media thickness (IMT).
    Design, setting, and participants: The analyses were performed in 2022 using data gathered from July 1989 through January 2018 within the Special Turku Coronary Risk Factor Intervention Project, a randomized, infancy-onset cohort of 534 participants coupled with annual BP (from age 7 months to 20 years), biennial IMT measurements (from ages 13 to 19 years), who were followed up with again at age 26 years.
    Exposures: BP measured from infancy (aged 7 to 13 months), preschool (2 to 5 years), childhood (6 to 12 years), adolescence (13 to 17 years), and young adulthood (18 to 26 years).
    Main outcomes and measures: Primary outcomes were carotid IMT measured in young adulthood at age 26 years. Bayesian relevant life-course exposure models assessed the relative contribution of BP at each life stage.
    Results: Systolic BP at each life stage contributed to the association with young adulthood carotid IMT (infancy: relative weight, 25.3%; 95% credible interval [CrI], 3.6-45.8; preschool childhood: relative weight, 27.0%; 95% CrI, 3.3-57.1; childhood: relative weight, 18.0%; 95% CrI, 0.5-40.0; adolescence: relative weight, 13.5%; 95% CrI, 0.4-37.1; and young adulthood: relative weight, 16.2%; 95% CrI, 1.6-46.1). A 1-SD (at single life-stage) higher systolic BP accumulated across the life course was associated with a higher carotid IMT (0.02 mm; 95% CrI, 0.01-0.03). The findings for carotid IMT were replicated in the Cardiovascular Risk in Young Finns Study that assessed systolic BP from childhood and carotid IMT in adulthood (33 to 45 years).
    Conclusion and relevance: In this cohort study, a life-course approach indicated that accumulation of risk exposure to BP levels at all life stages contributed to adulthood carotid IMT. Of those, the contribution attributed to each observed life stage was approximately equal. These results support prevention efforts that achieve and maintain normal BP levels across the life course, starting in infancy.
    MeSH term(s) Child, Preschool ; Adolescent ; Humans ; Young Adult ; Adult ; Child ; Blood Pressure/physiology ; Carotid Intima-Media Thickness ; Cohort Studies ; Life Change Events ; Bayes Theorem ; Risk Factors ; Cardiovascular Diseases
    Language English
    Publishing date 2023-12-04
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2701223-2
    ISSN 2168-6211 ; 2168-6203
    ISSN (online) 2168-6211
    ISSN 2168-6203
    DOI 10.1001/jamapediatrics.2023.5351
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  5. Article ; Online: Childhood risk factors and carotid atherosclerotic plaque in adulthood: The Cardiovascular Risk in Young Finns Study.

    Koskinen, Juhani S / Kytö, Ville / Juonala, Markus / Viikari, Jorma S A / Nevalainen, Jaakko / Kähönen, Mika / Lehtimäki, Terho / Hutri-Kähönen, Nina / Laitinen, Tomi / Tossavainen, Päivi / Jokinen, Eero / Magnussen, Costan G / Raitakari, Olli T

    Atherosclerosis

    2019  Volume 293, Page(s) 18–25

    Abstract: Background and aims: Carotid plaque is a specific sign of atherosclerosis and adults with carotid plaque are at increased risk for cardiovascular outcomes. Atherosclerosis has roots in childhood and pediatric guidelines provide cut-off values for ... ...

    Abstract Background and aims: Carotid plaque is a specific sign of atherosclerosis and adults with carotid plaque are at increased risk for cardiovascular outcomes. Atherosclerosis has roots in childhood and pediatric guidelines provide cut-off values for cardiovascular risk factors. However, it is unknown whether these cut-offs predict adulthood advanced atherosclerosis.
    Methods: The Cardiovascular Risk in Young Finns Study is a follow-up of children that begun in 1980 when 2653 participants with data for the present analyses were aged 3-18 years. In 2001 and 2007 follow-ups, in addition to adulthood cardiovascular risk factors, carotid ultrasound data was collected. Long-term burden, as the area under the curve, was evaluated for childhood (6-18 years) risk factors. To study the associations of guideline-based cut-offs with carotid plaque, both childhood and adult risk factors were classified according to clinical practice guidelines.
    Results: Carotid plaque, defined as a focal structure of the arterial wall protruding into lumen >50% compared to adjacent intima-media thickness, was present in 88 (3.3%) participants. Relative risk for carotid plaque, when adjusted for age and sex, was 3.03 (95% CI, 1.76-5.21) for childhood dyslipidemia, 1.51 (95% CI, 0.99-2.32) for childhood elevated systolic blood pressure, and 1.93 (95% CI, 1.26-2.94) for childhood smoking. Childhood dyslipidemia and smoking remained independent predictors of carotid plaque in models additionally adjusted for adult risk factors and family history of coronary heart disease. Carotid plaque was present in less than 1% of adults with no childhood risk factors.
    Conclusions: Findings reinforce childhood prevention efforts and demonstrate the utility of guideline-based cut-offs in identifying children at increased risk for adulthood atherosclerosis.
    MeSH term(s) Adolescent ; Blood Pressure/physiology ; Cardiovascular Diseases/diagnosis ; Cardiovascular Diseases/epidemiology ; Cardiovascular Diseases/etiology ; Carotid Arteries/diagnostic imaging ; Carotid Artery Diseases/complications ; Carotid Artery Diseases/diagnosis ; Carotid Artery Diseases/epidemiology ; Carotid Intima-Media Thickness ; Child ; Child, Preschool ; Disease Progression ; Female ; Finland/epidemiology ; Heart Disease Risk Factors ; Humans ; Incidence ; Male ; Plaque, Atherosclerotic/complications ; Plaque, Atherosclerotic/diagnosis ; Plaque, Atherosclerotic/epidemiology ; Ultrasonography
    Language English
    Publishing date 2019-11-30
    Publishing country Ireland
    Document type Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 80061-2
    ISSN 1879-1484 ; 0021-9150
    ISSN (online) 1879-1484
    ISSN 0021-9150
    DOI 10.1016/j.atherosclerosis.2019.11.029
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  6. Article ; Online: Serum Proteomic Profiling to Identify Biomarkers of Premature Carotid Atherosclerosis.

    Bhosale, Santosh D / Moulder, Robert / Venäläinen, Mikko S / Koskinen, Juhani S / Pitkänen, Niina / Juonala, Markus T / Kähönen, Mika A P / Lehtimäki, Terho J / Viikari, Jorma S A / Elo, Laura L / Goodlett, David R / Lahesmaa, Riitta / Raitakari, Olli T

    Scientific reports

    2018  Volume 8, Issue 1, Page(s) 9209

    Abstract: To evaluate the presence of serum protein biomarkers associated with the early phases of formation of carotid atherosclerotic plaques, label-free quantitative proteomics analyses were made for serum samples collected as part of The Cardiovascular Risk in ...

    Abstract To evaluate the presence of serum protein biomarkers associated with the early phases of formation of carotid atherosclerotic plaques, label-free quantitative proteomics analyses were made for serum samples collected as part of The Cardiovascular Risk in Young Finns Study. Samples from subjects who had an asymptomatic carotid artery plaque detected by ultrasound examination (N = 43, Age = 30-45 years) were compared with plaque free controls (N = 43) (matched for age, sex, body weight and systolic blood pressure). Seven proteins (p < 0.05) that have been previously linked with atherosclerotic phenotypes were differentially abundant. Fibulin 1 proteoform C (FBLN1C), Beta-ala-his-dipeptidase (CNDP1), Cadherin-13 (CDH13), Gelsolin (GSN) and 72 kDa type IV collagenase (MMP2) were less abundant in cases, whereas Apolipoproteins C-III (APOC3) and apolipoprotein E (APOE) were more abundant. Using machine learning analysis, a biomarker panel of FBLN1C, APOE and CDH13 was identified, which classified cases from controls with an area under receiver-operating characteristic curve (AUROC) value of 0.79. Furthermore, using selected reaction monitoring mass spectrometry (SRM-MS) the decreased abundance of FBLN1C was verified. In relation to previous associations of FBLN1C with atherosclerotic lesions, the observation could reflect its involvement in the initiation of the plaque formation, or represent a particular risk phenotype.
    MeSH term(s) Adult ; Blood Proteins/metabolism ; Carotid Artery Diseases/blood ; Carotid Artery Diseases/diagnostic imaging ; Female ; Finland ; Humans ; Male ; Middle Aged ; Plaque, Atherosclerotic/blood ; Plaque, Atherosclerotic/diagnostic imaging ; Proteome/metabolism ; Proteomics ; Ultrasonography
    Chemical Substances Blood Proteins ; Proteome
    Language English
    Publishing date 2018-06-15
    Publishing country England
    Document type Clinical Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-018-27265-9
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