Cargando…

Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis

Background: Heterozygous familial hypercholesterolemia (FH) is a common genetic disorder leading to premature cardiovascular disease and death as a result of lifelong high plasma low-density lipoprotein cholesterol levels, if not treated early in life. The prevalence of FH varies between countries b...

Descripción completa

Detalles Bibliográficos
Autores principales: Toft-Nielsen, Frida, Emanuelsson, Frida, Benn, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850281/
https://www.ncbi.nlm.nih.gov/pubmed/35186049
http://dx.doi.org/10.3389/fgene.2022.840797
_version_ 1784652560999645184
author Toft-Nielsen, Frida
Emanuelsson, Frida
Benn, Marianne
author_facet Toft-Nielsen, Frida
Emanuelsson, Frida
Benn, Marianne
author_sort Toft-Nielsen, Frida
collection PubMed
description Background: Heterozygous familial hypercholesterolemia (FH) is a common genetic disorder leading to premature cardiovascular disease and death as a result of lifelong high plasma low-density lipoprotein cholesterol levels, if not treated early in life. The prevalence of FH varies between countries because of founder effects, use of different diagnostic criteria, and screening strategies. However, little is known about differences in FH prevalence according to ethnicity. We aimed to investigate the ethnic distribution of FH in diverse populations and estimate the prevalence of FH according to ethnicity. Methods: We performed a systematic review and meta-analysis, searching PubMed and Web of Science for studies presenting data on the prevalence of heterozygous FH among different ethnicities in non-founder populations. Studies with more than 100 individuals, relevant data on prevalence, ethnicity, and using the Dutch Lipid Clinical Network Criteria, Simon Broome, Making Early Diagnosis Prevents Early Death, genetic screening, or comparable diagnostic criteria were considered eligible for inclusion. Results: Eleven general population studies and two patient studies were included in a systematic review and 11 general population studies in a random-effects meta-analysis. The overall pooled FH prevalence was 0.33% or 1:303 in 1,169,879 individuals (95% confidence interval: 0.26–0:40%; 1:385–1:250). Included studies presented data on six ethnicities: black, Latino, white, Asian, brown, and mixed/other. Pooled prevalence was estimated for each group. The highest prevalence observed was 0.52% or 1:192 among blacks (0.34–0.69%; 1:294–1:145) and 0.48% or 1:208 among browns (0.31–0.74%; 1:323–1:135) while the lowest pooled prevalence was 0.25% or 1:400 among Asians (0.15–0.35; 1:500–1:286). The prevalence was 0.37% or 1:270 among Latino (0.24–0.69%; 1:417–1:145), 0.31% or 1:323 among white (0.24–0.41%; 1:417–1:244), and 0.32% or 1:313 among mixed/other individuals (0.13–0.52%; 1:769–1:192). Conclusion: The estimated FH prevalence displays a variation across ethnicity, ranging from 0.25% (1:400) to 0.52% (1:192), with the highest prevalence seen among the black and brown and the lowest among the Asian individuals. The differences observed suggest that targeted screening among subpopulations may increase the identification of cases and thus the opportunity for prevention.
format Online
Article
Text
id pubmed-8850281
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88502812022-02-18 Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis Toft-Nielsen, Frida Emanuelsson, Frida Benn, Marianne Front Genet Genetics Background: Heterozygous familial hypercholesterolemia (FH) is a common genetic disorder leading to premature cardiovascular disease and death as a result of lifelong high plasma low-density lipoprotein cholesterol levels, if not treated early in life. The prevalence of FH varies between countries because of founder effects, use of different diagnostic criteria, and screening strategies. However, little is known about differences in FH prevalence according to ethnicity. We aimed to investigate the ethnic distribution of FH in diverse populations and estimate the prevalence of FH according to ethnicity. Methods: We performed a systematic review and meta-analysis, searching PubMed and Web of Science for studies presenting data on the prevalence of heterozygous FH among different ethnicities in non-founder populations. Studies with more than 100 individuals, relevant data on prevalence, ethnicity, and using the Dutch Lipid Clinical Network Criteria, Simon Broome, Making Early Diagnosis Prevents Early Death, genetic screening, or comparable diagnostic criteria were considered eligible for inclusion. Results: Eleven general population studies and two patient studies were included in a systematic review and 11 general population studies in a random-effects meta-analysis. The overall pooled FH prevalence was 0.33% or 1:303 in 1,169,879 individuals (95% confidence interval: 0.26–0:40%; 1:385–1:250). Included studies presented data on six ethnicities: black, Latino, white, Asian, brown, and mixed/other. Pooled prevalence was estimated for each group. The highest prevalence observed was 0.52% or 1:192 among blacks (0.34–0.69%; 1:294–1:145) and 0.48% or 1:208 among browns (0.31–0.74%; 1:323–1:135) while the lowest pooled prevalence was 0.25% or 1:400 among Asians (0.15–0.35; 1:500–1:286). The prevalence was 0.37% or 1:270 among Latino (0.24–0.69%; 1:417–1:145), 0.31% or 1:323 among white (0.24–0.41%; 1:417–1:244), and 0.32% or 1:313 among mixed/other individuals (0.13–0.52%; 1:769–1:192). Conclusion: The estimated FH prevalence displays a variation across ethnicity, ranging from 0.25% (1:400) to 0.52% (1:192), with the highest prevalence seen among the black and brown and the lowest among the Asian individuals. The differences observed suggest that targeted screening among subpopulations may increase the identification of cases and thus the opportunity for prevention. Frontiers Media S.A. 2022-02-03 /pmc/articles/PMC8850281/ /pubmed/35186049 http://dx.doi.org/10.3389/fgene.2022.840797 Text en Copyright © 2022 Toft-Nielsen, Emanuelsson and Benn. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Toft-Nielsen, Frida
Emanuelsson, Frida
Benn, Marianne
Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis
title Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis
title_full Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis
title_fullStr Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis
title_full_unstemmed Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis
title_short Familial Hypercholesterolemia Prevalence Among Ethnicities—Systematic Review and Meta-Analysis
title_sort familial hypercholesterolemia prevalence among ethnicities—systematic review and meta-analysis
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850281/
https://www.ncbi.nlm.nih.gov/pubmed/35186049
http://dx.doi.org/10.3389/fgene.2022.840797
work_keys_str_mv AT toftnielsenfrida familialhypercholesterolemiaprevalenceamongethnicitiessystematicreviewandmetaanalysis
AT emanuelssonfrida familialhypercholesterolemiaprevalenceamongethnicitiessystematicreviewandmetaanalysis
AT bennmarianne familialhypercholesterolemiaprevalenceamongethnicitiessystematicreviewandmetaanalysis