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Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting

BACKGROUND & OBJECTIVE: Heterozygous familial hypercholesterolemia (FHeH) is important risk factor for premature coronary artery disease (CAD). Strategies for its diagnosis and prevalence have not been well studied in India. We performed healthcare worker-based opportunistic screening to assess...

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Autores principales: Sharma, Sonali, Khudiwal, Ashish, Bhardwaj, Sonal, Chaturvedi, Hemant, Gupta, Rajeev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182245/
https://www.ncbi.nlm.nih.gov/pubmed/35679249
http://dx.doi.org/10.1371/journal.pone.0269605
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author Sharma, Sonali
Khudiwal, Ashish
Bhardwaj, Sonal
Chaturvedi, Hemant
Gupta, Rajeev
author_facet Sharma, Sonali
Khudiwal, Ashish
Bhardwaj, Sonal
Chaturvedi, Hemant
Gupta, Rajeev
author_sort Sharma, Sonali
collection PubMed
description BACKGROUND & OBJECTIVE: Heterozygous familial hypercholesterolemia (FHeH) is important risk factor for premature coronary artery disease (CAD). Strategies for its diagnosis and prevalence have not been well studied in India. We performed healthcare worker-based opportunistic screening to assess feasibility for determining its prevalence. METHODS: A healthcare worker was trained in use of Dutch Lipid Clinic Network (DLCN) criteria for diagnosis of FHeH. Successive eligible individuals (n = 3000 of 3450 screened) presenting to biochemistry laboratories of two hospitals for blood lipid measurements were evaluated for FHeH. Cascade screening or genetic studies were not performed. Descriptive statistics are reported. RESULTS: We included 2549 participants (men 1870, women 679) not on statin therapy. Health worker screened 25–30 individuals/day in 6–10 minutes each. The mean age was 46.2±11y. Variables of DLCN criteria were more in women vs men: family history 51.1 vs 35.6%, past CAD 48.2 vs 20.1%, arcus cornealis 1.1 vs 0.3%, tendon xanthoma 0.3 vs 0.1%, and LDL cholesterol 190–249 mg/dl in 8.5 vs 2.4%, 250–329 mg/dl in 0.7 vs 0% and ≥330 mg/dl in 0.3 vs 0% (p<0.01). Definite FHeH (DLCN score >8) was in 15 (0.59%, frequency 1:170) and probable FHeH (score 6–8) in 87 (3.4%, frequency 1:29). The prevalence was significantly greater in women, age <50y and in those with hypertension, diabetes and known CAD. CONCLUSIONS: Healthcare worker-led opportunistic screening for diagnosis of FHeH using DLCN criteria is feasible in low-resource settings. The results show significant prevalence of clinically detected definite and probable FHeH in the population studied.
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spelling pubmed-91822452022-06-10 Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting Sharma, Sonali Khudiwal, Ashish Bhardwaj, Sonal Chaturvedi, Hemant Gupta, Rajeev PLoS One Research Article BACKGROUND & OBJECTIVE: Heterozygous familial hypercholesterolemia (FHeH) is important risk factor for premature coronary artery disease (CAD). Strategies for its diagnosis and prevalence have not been well studied in India. We performed healthcare worker-based opportunistic screening to assess feasibility for determining its prevalence. METHODS: A healthcare worker was trained in use of Dutch Lipid Clinic Network (DLCN) criteria for diagnosis of FHeH. Successive eligible individuals (n = 3000 of 3450 screened) presenting to biochemistry laboratories of two hospitals for blood lipid measurements were evaluated for FHeH. Cascade screening or genetic studies were not performed. Descriptive statistics are reported. RESULTS: We included 2549 participants (men 1870, women 679) not on statin therapy. Health worker screened 25–30 individuals/day in 6–10 minutes each. The mean age was 46.2±11y. Variables of DLCN criteria were more in women vs men: family history 51.1 vs 35.6%, past CAD 48.2 vs 20.1%, arcus cornealis 1.1 vs 0.3%, tendon xanthoma 0.3 vs 0.1%, and LDL cholesterol 190–249 mg/dl in 8.5 vs 2.4%, 250–329 mg/dl in 0.7 vs 0% and ≥330 mg/dl in 0.3 vs 0% (p<0.01). Definite FHeH (DLCN score >8) was in 15 (0.59%, frequency 1:170) and probable FHeH (score 6–8) in 87 (3.4%, frequency 1:29). The prevalence was significantly greater in women, age <50y and in those with hypertension, diabetes and known CAD. CONCLUSIONS: Healthcare worker-led opportunistic screening for diagnosis of FHeH using DLCN criteria is feasible in low-resource settings. The results show significant prevalence of clinically detected definite and probable FHeH in the population studied. Public Library of Science 2022-06-09 /pmc/articles/PMC9182245/ /pubmed/35679249 http://dx.doi.org/10.1371/journal.pone.0269605 Text en © 2022 Sharma et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sharma, Sonali
Khudiwal, Ashish
Bhardwaj, Sonal
Chaturvedi, Hemant
Gupta, Rajeev
Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting
title Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting
title_full Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting
title_fullStr Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting
title_full_unstemmed Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting
title_short Healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting
title_sort healthcare worker-based opportunistic screening for familial hypercholesterolemia in a low-resource setting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182245/
https://www.ncbi.nlm.nih.gov/pubmed/35679249
http://dx.doi.org/10.1371/journal.pone.0269605
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