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Pregled bibliografske jedinice broj: 1274171

Apolipoprotein B, Residual Cardiovascular Risk After Acute Coronary Syndrome, and Effects of Alirocumab.


Hagström, E; Steg, PG; Szarek, M; Bhatt, DL; Bittner, VA; Danchin, N; Diaz, R; Goodman, SG; Harrington, RA; Jukema, JW et al.
Apolipoprotein B, Residual Cardiovascular Risk After Acute Coronary Syndrome, and Effects of Alirocumab. // Circulation, 146 (2022), 9; 657-672 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1274171 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Apolipoprotein B, Residual Cardiovascular Risk After Acute Coronary Syndrome, and Effects of Alirocumab.

Autori
Hagström, E ; Steg, PG ; Szarek, M ; Bhatt, DL ; Bittner, VA ; Danchin, N ; Diaz, R ; Goodman, SG ; Harrington, RA ; Jukema, JW ; Liberopoulos, E ; Marx, N ; McGinniss, J ; Manvelian, G ; Pordy, R ; Scemama, M ; White, HD ; Zeiher, AM ; Schwartz, GG ; ODYSSEY OUTCOMES Investigators, Lovric Bencic, M

Izvornik
Circulation (0009-7322) 146 (2022), 9; 657-672

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
PCSK9 inhibitors, acute coronary syndrome, apolipoproteins B, LDL cholesterol

Sažetak
The ODYSSEY OUTCOMES trial (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab) compared the proprotein convertase subtilisin/kexin type 9 inhibitor alirocumab with placebo in 18 924 patients with recent acute coronary syndrome and elevated atherogenic lipoproteins despite optimized statin therapy. Primary outcome was major adverse cardiovascular events (MACE ; coronary heart disease death, nonfatal myocardial infarction, fatal/nonfatal ischemic stroke, hospitalization for unstable angina). Associations between baseline apoB or apoB at 4 months and MACE were assessed in adjusted Cox proportional hazards and propensity score-matched models. Results: Median follow-up was 2.8 years. In proportional hazards analysis in the placebo group, MACE incidence increased across increasing baseline apoB strata (3.2 [95% CI, 2.9-3.6], 4.0 [95% CI, 3.6-4.5], and 5.5 [95% CI, 5.0-6.1] events per 100 patient-years in strata <75, 75-<90, ≥90 mg/dL, respectively ; Ptrend<0.0001) and after adjustment for low-density lipoprotein cholesterol (Ptrend=0.035). Higher baseline apoB stratum was associated with greater relative (Ptrend<0.0001) and absolute reduction in MACE with alirocumab versus placebo. In the alirocumab group, the incidence of MACE after month 4 decreased monotonically across decreasing achieved apoB strata (4.26 [95% CI, 3.78-4.79], 3.09 [95% CI, 2.69- 3.54], and 2.41 [95% CI, 2.11-2.76] events per 100 patient-years in strata ≥50, >35-<50, and ≤35 mg/dL, respectively). Compared with propensity score-matched patients from the placebo group, treatment hazard ratios for alirocumab also decreased monotonically across achieved apoB strata. Achieved apoB was predictive of MACE after adjustment for achieved low-density lipoprotein cholesterol or non-high-density lipoprotein cholesterol but not vice versa.

Izvorni jezik
Engleski



POVEZANOST RADA


Ustanove:
Medicinski fakultet, Zagreb


Citiraj ovu publikaciju:

Hagström, E; Steg, PG; Szarek, M; Bhatt, DL; Bittner, VA; Danchin, N; Diaz, R; Goodman, SG; Harrington, RA; Jukema, JW et al.
Apolipoprotein B, Residual Cardiovascular Risk After Acute Coronary Syndrome, and Effects of Alirocumab. // Circulation, 146 (2022), 9; 657-672 (međunarodna recenzija, članak, znanstveni)
Hagström, E., Steg, P., Szarek, M., Bhatt, D., Bittner, V., Danchin, N., Diaz, R., Goodman, S., Harrington, R. & Jukema, J. (2022) Apolipoprotein B, Residual Cardiovascular Risk After Acute Coronary Syndrome, and Effects of Alirocumab.. Circulation, 146 (9), 657-672.
@article{article, author = {Hagstr\"{o}m, E and Steg, PG and Szarek, M and Bhatt, DL and Bittner, VA and Danchin, N and Diaz, R and Goodman, SG and Harrington, RA and Jukema, JW and Liberopoulos, E and Marx, N and McGinniss, J and Manvelian, G and Pordy, R and Scemama, M and White, HD and Zeiher, AM and Schwartz, GG}, year = {2022}, pages = {657-672}, keywords = {PCSK9 inhibitors, acute coronary syndrome, apolipoproteins B, LDL cholesterol}, journal = {Circulation}, volume = {146}, number = {9}, issn = {0009-7322}, title = {Apolipoprotein B, Residual Cardiovascular Risk After Acute Coronary Syndrome, and Effects of Alirocumab.}, keyword = {PCSK9 inhibitors, acute coronary syndrome, apolipoproteins B, LDL cholesterol} }
@article{article, author = {Hagstr\"{o}m, E and Steg, PG and Szarek, M and Bhatt, DL and Bittner, VA and Danchin, N and Diaz, R and Goodman, SG and Harrington, RA and Jukema, JW and Liberopoulos, E and Marx, N and McGinniss, J and Manvelian, G and Pordy, R and Scemama, M and White, HD and Zeiher, AM and Schwartz, GG}, year = {2022}, pages = {657-672}, keywords = {PCSK9 inhibitors, acute coronary syndrome, apolipoproteins B, LDL cholesterol}, journal = {Circulation}, volume = {146}, number = {9}, issn = {0009-7322}, title = {Apolipoprotein B, Residual Cardiovascular Risk After Acute Coronary Syndrome, and Effects of Alirocumab.}, keyword = {PCSK9 inhibitors, acute coronary syndrome, apolipoproteins B, LDL cholesterol} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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