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Hypertrophic cardiomyopathy in Nigeria: protocol for a systematic review
Okechukwu S Ogah1,2, Franklin Obiekwe3, Oluwadamilotun Oguntuga3
1Cardiology Unit, Department of Medicine, University of Ibadan, Ibadan, Oyo state, Nigeria. osogah56156@gmail.com.
Insights
This systematic review examines hypertrophic cardiomyopathy (HCM) in Nigeria, a leading cause of sudden cardiac death. It aims to consolidate existing data on HCM prevalence and clinical characteristics within the country.
Area of Science:
- Cardiology
- Genetics
- Public Health
Background:
- Hypertrophic cardiomyopathy (HCM) is a significant global cause of sudden cardiac death, often inherited in an autosomal dominant pattern.
- While advancements have improved HCM outcomes, data from Nigeria are scarce, with most research concentrated in single centers.
- This systematic review addresses the limited understanding of HCM in Nigeria.
Purpose of the Study:
- To conduct the first systematic review on the prevalence and clinical profile of hypertrophic cardiomyopathy in Nigeria.
- To identify research gaps and inform future studies on HCM in the Nigerian population.
Main Methods:
- A comprehensive search of multiple databases (PubMed/Medline, EMBASE, Web of Science, Google Scholar, African Index Medicus, African Journal Online) will be performed.
- Articles published in English from 1960 to 2024, including case reports, case control, cross-sectional, and cohort studies, will be analyzed.
- Three independent reviewers will manage article selection and data extraction.
Main Results:
- The review will report on the prevalence of HCM in Nigeria.
- It will detail the clinical profile and characteristics of HCM patients in Nigeria.
Conclusions:
- This study represents the first systematic review focusing on HCM prevalence and clinical presentation in Nigeria.
- The findings are expected to highlight areas for future research and improve understanding of HCM within the Nigerian context.
Background:
Hypertrophic cardiomyopathy(HCM) is one of the common causes of sudden cardiac death worldwide. It is an autosomal dominant condition with a global distribution. Historically associated with a poor prognosis, advancements in cardiac imaging and management strategies have significantly improved outcomes, reducing morbidity and mortality. Although extensive research on HCM exists in more developed countries, data from Nigeria remain limited, with most studies originating from single centers.
Methods:
Relevant databases such as PubMed /Medline, EMBASE, Web of Science, Google Scholar, African Index Medicus, and African Journal Online will be searched for articles published in English from January 1, 1960 to December 31, 2024. The analysis will include case reports, case control, cross-sectional, and cohort studies that reported the prevalence, risk factors, clinical profile, and outcomes of the condition. Three independent reviewers shall conduct article selection. Data extraction shall be done by 3 independent reviewers.
Results:
The outcome measures will include the prevalence, clinical profile and characteristics of HCM in Nigeria.
Registration Details:
This systematic review has been registered on the International Prospective Register of Systematic Reviews (PROSPERO), protocol no: CRD420251020441.
Clinical Trial Number:
Not Applicable.
Conclusion:
This will be the first systematic review on the prevalence and clinical profile of HCM in Nigeria which will hopefully identify gaps for future research.
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