Prevalence and significance of isolated left ventricular non-compaction phenotype in normal black Africans using echocardiography.

CHBH, Chris Hani Baragwanath Hospital Echocardiography ILVNC, isolated left ventricular noncompaction IVSd, interventricular septal wall thickness in diastole LVEDD, left ventricular end-diastolic diameter NC/C, noncompacted to compacted Normal PWD, posterior wall thickness in diastole Trabeculations

Journal

International journal of cardiology. Heart & vasculature
ISSN: 2352-9067
Titre abrégé: Int J Cardiol Heart Vasc
Pays: Ireland
ID NLM: 101649525

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 30 06 2020
accepted: 02 07 2020
entrez: 28 7 2020
pubmed: 28 7 2020
medline: 28 7 2020
Statut: epublish

Résumé

Several large, prospective screening studies of predominantly Caucasian patients have suggested that hypertrabeculation may not necessarily be pathologic unless there is concomitant left ventricular (LV) dysfunction, LV dilatation, history of arrhythmia, family history, or characteristic gene mutations. This conundrum may be magnified in blacks, in whom hypertrabeculation and LV hypertrophy is more common. We therefore investigated the frequency of hypertrabeculation/isolated LV noncompaction (ILVNC) phenotype in normal black Africans and evaluated LV function using sensitive measures of deformation and twist. Two hundred and fifty-three volunteers were recruited and evaluated according to strict inclusion and exclusion criteria. Their mean age was 36.3 ± 12.2 years. Trabeculations were found in 12 (4.74%) participants. Three (1.2%) subjects had ≥ 4 LV trabeculations. The LV apex was the most common anatomical site for the location of trabeculations. Subjects with trabeculations were more likely to be males of a younger age, and had greater LV end-diastolic and end-systolic parameters and lateral e'. However, 0.8% of the population fulfilled the Stollberger criteria, and none fulfilled the Jenni, Milwaukee, or Baragwanath criteria. All subjects in this study had normal rotation patterns with no differences in rotational parameters or net twist. Trabeculations may be found as a normal variant in black Africans. Assessing trabeculations alone may infer ILVNC; however, utilizing the more comprehensive ILVNC criteria enables differentiation of a possible LVNC phenotype. Normal individuals with hypertrabeculation have normal LV function and normal rotation patterns, with no differences in rotational parameters or net twist.

Sections du résumé

BACKGROUND BACKGROUND
Several large, prospective screening studies of predominantly Caucasian patients have suggested that hypertrabeculation may not necessarily be pathologic unless there is concomitant left ventricular (LV) dysfunction, LV dilatation, history of arrhythmia, family history, or characteristic gene mutations. This conundrum may be magnified in blacks, in whom hypertrabeculation and LV hypertrophy is more common. We therefore investigated the frequency of hypertrabeculation/isolated LV noncompaction (ILVNC) phenotype in normal black Africans and evaluated LV function using sensitive measures of deformation and twist.
METHODS METHODS
Two hundred and fifty-three volunteers were recruited and evaluated according to strict inclusion and exclusion criteria. Their mean age was 36.3 ± 12.2 years.
RESULTS RESULTS
Trabeculations were found in 12 (4.74%) participants. Three (1.2%) subjects had ≥ 4 LV trabeculations. The LV apex was the most common anatomical site for the location of trabeculations. Subjects with trabeculations were more likely to be males of a younger age, and had greater LV end-diastolic and end-systolic parameters and lateral e'. However, 0.8% of the population fulfilled the Stollberger criteria, and none fulfilled the Jenni, Milwaukee, or Baragwanath criteria. All subjects in this study had normal rotation patterns with no differences in rotational parameters or net twist.
CONCLUSIONS CONCLUSIONS
Trabeculations may be found as a normal variant in black Africans. Assessing trabeculations alone may infer ILVNC; however, utilizing the more comprehensive ILVNC criteria enables differentiation of a possible LVNC phenotype. Normal individuals with hypertrabeculation have normal LV function and normal rotation patterns, with no differences in rotational parameters or net twist.

Identifiants

pubmed: 32715082
doi: 10.1016/j.ijcha.2020.100585
pii: S2352-9067(20)30283-9
pii: 100585
pmc: PMC7378683
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100585

Informations de copyright

© 2020 The Authors.

Déclaration de conflit d'intérêts

The authors declared that there is no conflict of interest.

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Auteurs

Samantha Nel (S)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.

Bijoy K Khandheria (BK)

Aurora Cardiovascular and Thoracic Services, Aurora Sinai/Aurora St. Luke's Medical Centers, University of Wisconsin School of Medicine and Public Health, Marcus Family Fund for Echocardiography (ECHO) Research and Education, 2801 W. Kinnickinnic River Parkway, Ste. 880, Milwaukee, WI, 53215, USA.

Elena Libhaber (E)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.

Ferande Peters (F)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.
Cardiovascular Pathophysiology and Genomics unit, University of the Witwatersrand, 7 York Road, Parktown 2193, Johannesburg, South Africa.

Claudia Ferreira Dos Santos (C)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.
Cardiovascular Pathophysiology and Genomics unit, University of the Witwatersrand, 7 York Road, Parktown 2193, Johannesburg, South Africa.

Hiral Matioda (H)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.

Sacha Grinter (S)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.

Nirvathi Maharaj (N)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.
Cardiovascular Pathophysiology and Genomics unit, University of the Witwatersrand, 7 York Road, Parktown 2193, Johannesburg, South Africa.

Mohammed R Essop (MR)

Division of Cardiology, Chris Hani Baragwanath Academic Hospital and University of the Witwatersrand, R68 Old Potchefstroom Road, PO Bertsham, Johannesburg 2013, South Africa.

Classifications MeSH