Elevated Lp(a) is a common, genetically determined trait in Africa rather than a rare dyslipidemia, acting as a significant amplifier of cardiovascular risk, particularly in the presence of rising incident rates of hypertension and diabetes.
Key Findings
Results
Studies in Ghana reported prevalence rates of elevated Lp(a) (>30 mg/dL) between 30–61% among apparently healthy individuals.
The threshold used to define elevated Lp(a) was >30 mg/dL.
Ghana was among the most represented countries in the review.
This prevalence range was derived from observational studies in apparently healthy adults aged ≥18 years.
The wide range (30–61%) reflects variation across cohorts and assay methods used.
Results
Mean Lp(a) levels across African cohorts ranged from 12.7 mg/dL to 54.5 mg/dL depending on the cohort and assay used.
The large range highlights substantial heterogeneity across populations and measurement approaches.
Variation was attributed to both cohort characteristics and differences in assay methods.
Studies were drawn from West Africa (Nigeria, Ghana), Central Africa (Cameroon), Southern Africa (South Africa, Zimbabwe), and North Africa (Morocco, Tunisia).
Assay standardization was identified as a major methodological concern affecting comparability.
Results
Females exhibited higher Lp(a) levels than males across most African cohorts included in the review.
This sex-based difference in Lp(a) levels was observed consistently across most studies.
The finding was noted across multiple African regions and ethnic groups.
No specific numerical sex-disaggregated values were reported in the abstract.
This pattern is consistent with some findings in non-African populations but was specifically documented here in African cohorts.
Results
Elevated Lp(a) was clinically associated with hypertension, type 2 diabetes mellitus, ischemic stroke, myocardial infarction, and antiretroviral drug use in African populations.
These associations were identified across the 17 included observational studies.
Study designs included cross-sectional, cohort, and case-control studies.
The association with antiretroviral drug use is a notable and distinct finding relevant to Africa's HIV burden.
The review characterized elevated Lp(a) as a 'significant amplifier of cardiovascular risk, particularly in the presence of rising incident rates of hypertension and diabetes.'
Methods
A total of 17 studies met the inclusion criteria, representing populations from West, Central, Southern, and North Africa.
Countries represented included Nigeria, Ghana (West Africa), Cameroon (Central Africa), South Africa and Zimbabwe (Southern Africa), and Morocco and Tunisia (North Africa).
Studies were identified by searching PubMed/MEDLINE, Embase, Scopus, African Journals Online, and Google Scholar without language or date restrictions.
Methodological quality was assessed using the Newcastle-Ottawa Scale.
The review included only apparently healthy adults aged ≥18 years residing on the African continent.
Large portions of the African continent, including East Africa, were notably absent from the included literature.
Conclusions
The review concluded that elevated Lp(a) is a common, genetically determined trait in Africa rather than a rare dyslipidemia.
Lp(a) is encoded by the LPA gene and is described as covalently bound to apolipoprotein(a).
The review characterized it as 'a well-established, independent, and causal risk factor for cardiovascular disease.'
The authors contrasted this with the existing literature, which has 'extensively mapped' Lp(a) epidemiology in non-African populations while African populations remain 'under-characterized.'
Africa's 'unique genetic, phenotypic, ethnolinguistic and ancestral diversity' was cited as a reason why dedicated study is needed.
Conclusions
The review identified a need for standardized, isoform-independent assays and population-specific risk thresholds for African populations.
Current assay heterogeneity was identified as a key barrier to comparability across African studies.
Isoform-independent assays were specifically recommended to address variation in Lp(a) particle size.
Population-specific risk thresholds were recommended to guide 'targeted preventive cardiovascular care.'
The lack of standardization was highlighted as contributing to the wide range of observed mean Lp(a) levels (12.7–54.5 mg/dL).
What This Means
This research systematically reviewed 17 studies examining levels of a blood particle called Lipoprotein(a), or Lp(a), in apparently healthy people living across Africa. Lp(a) is a genetically determined molecule in the blood that, when elevated, significantly increases the risk of heart attacks, strokes, and other cardiovascular diseases. The review found that elevated Lp(a) is surprisingly common in African populations — in Ghana alone, between 30% and 61% of apparently healthy individuals had levels considered clinically elevated (above 30 mg/dL). Women tended to have higher Lp(a) levels than men across most African populations studied. Elevated Lp(a) was also linked to serious conditions including high blood pressure, type 2 diabetes, ischemic stroke, heart attack, and use of antiretroviral drugs (medications used to treat HIV).
This research suggests that high Lp(a) is not a rare or unusual finding in Africa — it appears to be a common genetic trait that may be amplifying cardiovascular risk across the continent, especially as rates of diabetes and hypertension continue to rise. Despite this, the condition remains largely unstudied and unrecognized in African healthcare settings. The review also highlighted that different studies used different measurement methods, making it difficult to directly compare results or establish clear cutoffs for what constitutes a dangerous level in African populations specifically.
The practical implication of this research is that Africa may be facing a largely hidden cardiovascular risk factor affecting a substantial proportion of its population. The authors call for adoption of standardized testing methods and the development of Africa-specific guidelines for Lp(a) screening and risk management. Addressing this gap could be important for improving cardiovascular disease prevention and care across the continent, particularly as new therapies targeting Lp(a) are being developed globally.