Lack of morphometric evidence for ventricular compaction in humans. Issue 5 (November 2021)

• Record Type: Journal Article
• Authors: Faber, Jaeike W.; D'Silva, Andrew; Christoffels, Vincent M.; Jensen, Bjarke
• Is Part Of: Journal of cardiology. Volume 78:Issue 5(2021)
• Page Start: 397
• Page End: 405
• Publication Date: 2021-11
• Subjects: Left ventricular non-compaction -- Cardiac development -- Ventricular anatomy -- Trabeculation -- Comparative anatomy; Cardiology -- Periodicals; 616.12
• DOI: 10.1016/j.jjcc.2021.03.006
• Languages: English
• ISSNs: 0914-5087

Abstract

Highlights: Quantifying ventricular wall development in humans shows no evidence for compaction. In mice, some compaction might take place. In chickens, compaction is pronounced. Excessive trabecular formation (in mice) yields a noncompacted phenotype. Abstract: The remodeling of the compact wall by incorporation of trabecular myocardium, referred to as compaction, receives much attention because it is thought that its failure causes left ventricular non-compaction cardiomyopathy (LVNC). Although the notion of compaction is broadly accepted, the nature and strength of the evidence supporting this process is underexposed. Here, we review the literature that quantitatively investigated the development of the ventricular wall to understand the extent of compaction in humans, mice, and chickens. We queried PubMed using several search terms, screened 1127 records, and selected 56 publications containing quantitative data on ventricular growth. For humans, only 34 studies quantified wall development. The key premise of compaction, namely a reduction of the trabecular layer, was never documented. Instead, the trabecular layer grows slower than the compact wall in later development and this changes wall architecture. There were no reports of a sudden enlargement of the compact layer (from incorporated trabeculae), be it in thickness, area, or volume. Therefore, no evidence for compaction was found. Only in chickens, a sudden increase in compact myocardial thickness layer was reported coinciding with a decrease in trabecular thickness. In mice, morphometric and lineage tracing investigations have yielded conflicting results that allow for limited compaction to occur. In conclusion, compaction in human development is not supported while rapid intrinsic growth of the compact wall is supported in all species. If compaction takes place, it likely plays a much smaller role in determining wall architecture than intrinsic growth of the compact wall.