Lipoprotein(a) in Youth and Prediction of Major Cardiovascular Outcomes in Adulthood

Author:

Raitakari Olli123ORCID,Kartiosuo Noora12,Pahkala Katja124,Hutri-Kähönen Nina5,Bazzano Lydia A.6ORCID,Chen Wei6ORCID,Urbina Elaine M.78ORCID,Jacobs David R.9ORCID,Sinaiko Alan10ORCID,Steinberger Julia10,Burns Trudy11,Daniels Stephen R.1213,Venn Alison14ORCID,Woo Jessica G.715ORCID,Dwyer Terry141617ORCID,Juonala Markus1118ORCID,Viikari Jorma11ORCID

Affiliation:

1. Centre for Population Health Research, University of Turku and Turku University Hospital, Finland (O.R., N.K., K.P.).

2. Research Centre of Applied and Preventive Cardiovascular Medicine (O.R., N.K., K.P.), University of Turku, Finland.

3. Department of Clinical Physiology and Nuclear Medicine (O.R.), Turku University Hospital, Finland.

4. Paavo Nurmi Centre and Unit for Health and Physical Activity (K.P.), University of Turku, Finland.

5. Tampere Centre for Skills Training and Simulation, Tampere University, Finland (N.H.-K.).

6. Department of Epidemiology, School of Public Health and Tropical Medicine, Tulane University, New Orleans, LA (L.A.B., W.C.).

7. Department of Pediatrics, University of Cincinnati College of Medicine, OH (E.M.U., J.G.W.).

8. The Heart Institute (E.M.U.), Cincinnati Children’s Hospital Medical Center, OH.

9. Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis (D.R.J.).

10. Department of Pediatrics, University of Minnesota Medical School, Minneapolis (A.S., J.S.).

11. Department of Medicine (M.J., J.V.), University of Turku, Finland.

12. Department of Pediatrics, University of Colorado School of Medicine, Aurora (S.R.D.).

13. Children’s Hospital Colorado, Anschutz Medical Campus, Aurora (S.R.D.).

14. Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia (A.V., T.D.).

15. Division of Biostatistics and Epidemiology (J.G.W.), Cincinnati Children’s Hospital Medical Center, OH.

16. Heart Research Group, Murdoch Children’s Research Institute, Melbourne, Australia (T.D.).

17. Nuffield Department of Women’s & Reproductive Health, University of Oxford, United Kingdom (T.D.).

18. Division of Medicine (M.J., J.V.), Turku University Hospital, Finland.

Abstract

Background: Elevated lipoprotein(a) [Lp(a)] is a common risk factor for cardiovascular disease outcomes with unknown mechanisms. We examined its potential role in identifying youths who are at increased risk of developing adult atherosclerotic cardiovascular disease (ASCVD). Methods: Lp(a) levels measured in youth 9 to 24 years of age were linked to adult ASCVD and carotid intima-media thickness in the YFS (Cardiovascular Risk in Young Finns Study), in which 95 of the original 3596 participants (2.7%) recruited as children have been diagnosed with ASCVD at a median of 47 years of age. Results observed in YFS were replicated with the use of data for White participants from the BHS (Bogalusa Heart Study). In BHS, 587 White individuals had data on youth Lp(a) (measured at 8–17 years of age) and information on adult events, including 15 cases and 572 noncases. Analyses were performed with the use of Cox proportional hazard regression. Results: In YFS, those who had been exposed to high Lp(a) level in youth [defined as Lp(a) ≥30 mg/dL] had ≈2 times greater risk of developing adult ASCVD compared with nonexposed individuals (hazard ratio, 2.0 [95% CI, 1.4–2.6]). Youth risk factors, including Lp(a), low-density lipoprotein cholesterol, body mass index, and smoking, were all independently associated with higher risk. In BHS, in an age- and sex-adjusted model, White individuals who had been exposed to high Lp(a) had 2.5 times greater risk (95% CI, 0.9–6.8) of developing adult ASCVD compared with nonexposed individuals. When also adjusted for low-density lipoprotein cholesterol and body mass index, the risk associated with high Lp(a) remained unchanged (hazard ratio, 2.4 [95% CI, 0.8–7.3]). In a multivariable model for pooled data, individuals exposed to high Lp(a) had 2.0 times greater risk (95% CI, 1.0–3.7) of developing adult ASCVD compared with nonexposed individuals. No association was detected between youth Lp(a) and adult carotid artery thickness in either cohort or pooled data. Conclusions: Elevated Lp(a) level identified in youth is a risk factor for adult atherosclerotic cardiovascular outcomes but not for increased carotid intima-media thickness.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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