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Estudio2021

Lp(a) (Lipoprotein[a]) Concentrations and Incident Atherosclerotic Cardiovascular Disease: New Insights From a Large National Biobank

Patel AP, Wang (汪敏先) M, Pirruccello JP, Ellinor PT, Ng K, Kathiresan S, Khera AV

Arteriosclerosis, thrombosis, and vascular biology · 487 citas

Cómo se estudió

Diseño
Estudio de cohortes (clasificado por nuestro filtro de IA)
Estudiado en
Personas
Resultado principal
Eventos clínicos como enfermedad o muerte

Quién lo pagó

Financiación
Financiación independiente
Organización sin fines de lucro
American Heart Association
Universidad u hospital
Massachusetts General Hospital
Universidad u hospital
Broad Institute
Organización sin fines de lucro
Fondation Leducq
Gobierno
Medical Research Council
Gobierno
National Heart, Lung, and Blood Institute
Gobierno
National Human Genome Research Institute
Gobierno
NHLBI NIH HHS
Gobierno
NHGRI NIH HHS
Subvenciones
National Heart, Lung, and Blood Institute (T32 HL 007208); National Heart, Lung, and Blood Institute (1RO1HL092577); Fondation Leducq (K24HL105780); National Human Genome Research Institute (K08HG010155); Fondation Leducq (18SFRN34110082); National Heart, Lung, and Blood Institute (K24 HL105780); American Heart Association (R01 HL128914); National Heart, Lung, and Blood Institute (R01HL128914); National Heart, Lung, and Blood Institute (R01 HL092577); Medical Research Council (MC_PC_17228); American Heart Association (18SFRN34110082); Fondation Leducq (1RO1HL092577); Fondation Leducq (T32HL007208); National Human Genome Research Institute (18SFRN34110082); Fondation Leducq (14CVD01); Fondation Leducq (R01HL128914)

Según 9 financiadores declarados.

Publicación

Publicado
2020-10-29 · Arterioscler Thromb Vasc Biol · vol. 41 · número 1 · págs. 465–474
Editorial
Lippincott Williams & Wilkins
Citado
563 citas · más que el 100% de estudios similares · 35.9× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
50 trabajos
Acceso
Acceso abierto (revista híbrida) · OTHER-OA
Áreas de investigación
Lipoproteins and Cardiovascular Health · Atherosclerosis and Cardiovascular Diseases · Diabetes, Cardiovascular Risks, and Lipoproteins
Palabras clave
lipoprotein(a), atherosclerotic cardiovascular disease, incident cardiovascular events, racial differences, risk gradient, primary prevention, secondary prevention, middle-aged adults, UK Biobank
MeSH
humans, lipoprotein(a), prognosis, incidence, risk assessment, primary prevention, time factors, adult, aged, middle aged, biological specimen banks, female, male, atherosclerosis, secondary prevention, biomarkers, united kingdom, race factors, heart disease risk factors

7 autores

  • Aniruddh P. Patel🇺🇸Broad Institute; Harvard University; Massachusetts General Hospital; Massachusetts Institute of Technology
  • Minxian Wang🇺🇸Broad Institute; Harvard University; Massachusetts Institute of Technology
  • James P. Pirruccello🇺🇸Broad Institute; Harvard University; Massachusetts General Hospital; Massachusetts Institute of Technology
  • Patrick T. Ellinor🇺🇸Broad Institute; Harvard University; Massachusetts General Hospital; Massachusetts Institute of Technology
  • Kenney Ng🇺🇸IBM (United States)
  • Sekar Kathiresan🇺🇸Broad Institute; Harvard University; Massachusetts General Hospital; Verve Therapeutics (United States); Massachusetts Institute of Technology
  • Amit V. Khera🇺🇸 · autor de correspondenciaBroad Institute; Harvard University; Massachusetts General Hospital; Massachusetts Institute of Technology

Resumen

El texto original del estudio, en el idioma en que se publicó.

Objective

Lp(a) (lipoprotein[a]) concentrations are associated with atherosclerotic cardiovascular disease (ASCVD), and new therapies that enable potent and specific reduction are in development. In the largest study conducted to date, we address 3 areas of uncertainty: (1) the magnitude and shape of ASCVD risk conferred across the distribution of lipoprotein(a) concentrations; (2) variation of risk across racial and clinical subgroups; (3) clinical importance of a high lipoprotein(a) threshold to guide therapy. Approach and Results: Relationship of lipoprotein(a) to incident ASCVD was studied in 460 506 middle-aged UK Biobank participants. Over a median follow-up of 11.2 years, incident ASCVD occurred in 22 401 (4.9%) participants. Median lipoprotein(a) concentration was 19.6 nmol/L (25th-75th percentile 7.6-74.8). The relationship between lipoprotein(a) and ASCVD appeared linear across the distribution, with a hazard ratio of 1.11 (95% CI, 1.10-1.12) per 50 nmol/L increment. Substantial differences in concentrations were noted according to race-median values for white, South Asian, black, and Chinese individuals were 19, 31, 75, and 16 nmol/L, respectively. However, risk per 50 nmol/L appeared similar-hazard ratios of 1.11, 1.10, and 1.07 for white, South Asian, and black individuals, respectively. A high lipoprotein(a) concentration defined as ≥150 nmol/L was present in 12.2% of those without and 20.3% of those with preexisting ASCVD and associated with hazard ratios of 1.50 (95% CI, 1.44-1.56) and 1.16 (95% CI, 1.05-1.27), respectively.

Conclusions

Lipoprotein(a) concentrations predict incident ASCVD among middle-aged adults within primary and secondary prevention contexts, with a linear risk gradient across the distribution. Concentrations are variable across racial subgroups, but the associated risk appears similar.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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