TY - JOUR
T1 - High lipoprotein(a) is a risk factor for peripheral artery disease, abdominal aortic aneurysms, and major adverse limb events
AU - Thomas, Peter E.
AU - Vedel-Krogh, Signe
AU - Kamstrup, Pia R.
N1 - Publisher Copyright:
Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.
PY - 2024/11/1
Y1 - 2024/11/1
N2 - Purpose of review To summarize evidence from recent studies of high lipoprotein(a) as a risk factor for peripheral artery disease (PAD), abdominal aortic aneurysms (AAA), and major adverse limb events (MALE). Additionally, provide clinicians with 10-year absolute risk charts enabling risk prediction of PAD and AAA by lipoprotein(a) levels and conventional risk factors. Recent findings Numerous studies support high lipoprotein(a) as an independent risk factor for PAD, AAA, and MALE. The strongest evidence is from the Copenhagen General Population Study (CGPS) and the UK Biobank, two large general population-based cohorts. In the CGPS, a 50 mg/dl higher genetically determined lipoprotein(a) associated with hazard ratios of 1.39 (1.24–1.56) for PAD and 1.21 (1.01–1.44) for AAA. Corresponding hazard ratio in the UK Biobank were 1.38 (1.30–1.46) and 1.42 (1.28–1.59). In CGPS participants with levels at least 99th (≥143 mg/dl) vs, less than 50th percentile (≤9 mg/dl), hazard ratios were 2.99 (2.09–4.30) for PAD and 2.22 (1.21–4.07) for AAA, with a corresponding incidence rate ratio for MALE of 3.04 (1.55–5.98) in participants with PAD. Summary Evidence from both observational and genetic studies support high lipoprotein(a) as a causal risk factor for PAD, AAA, and MALE, and highlight the potential of future lipoprotein(a)-lowering therapy to reduce the substantial morbidity and mortality associated with these diseases.
AB - Purpose of review To summarize evidence from recent studies of high lipoprotein(a) as a risk factor for peripheral artery disease (PAD), abdominal aortic aneurysms (AAA), and major adverse limb events (MALE). Additionally, provide clinicians with 10-year absolute risk charts enabling risk prediction of PAD and AAA by lipoprotein(a) levels and conventional risk factors. Recent findings Numerous studies support high lipoprotein(a) as an independent risk factor for PAD, AAA, and MALE. The strongest evidence is from the Copenhagen General Population Study (CGPS) and the UK Biobank, two large general population-based cohorts. In the CGPS, a 50 mg/dl higher genetically determined lipoprotein(a) associated with hazard ratios of 1.39 (1.24–1.56) for PAD and 1.21 (1.01–1.44) for AAA. Corresponding hazard ratio in the UK Biobank were 1.38 (1.30–1.46) and 1.42 (1.28–1.59). In CGPS participants with levels at least 99th (≥143 mg/dl) vs, less than 50th percentile (≤9 mg/dl), hazard ratios were 2.99 (2.09–4.30) for PAD and 2.22 (1.21–4.07) for AAA, with a corresponding incidence rate ratio for MALE of 3.04 (1.55–5.98) in participants with PAD. Summary Evidence from both observational and genetic studies support high lipoprotein(a) as a causal risk factor for PAD, AAA, and MALE, and highlight the potential of future lipoprotein(a)-lowering therapy to reduce the substantial morbidity and mortality associated with these diseases.
KW - abdominal aortic aneurysm
KW - lipoprotein(a)
KW - major adverse limb event
KW - peripheral artery disease
KW - primary prevention
KW - secondary prevention
UR - http://www.scopus.com/inward/record.url?scp=85205604419&partnerID=8YFLogxK
U2 - 10.1097/HCO.0000000000001168
DO - 10.1097/HCO.0000000000001168
M3 - Review
C2 - 39356276
AN - SCOPUS:85205604419
SN - 0268-4705
VL - 39
SP - 511
EP - 519
JO - Current Opinion in Cardiology
JF - Current Opinion in Cardiology
IS - 6
ER -