PMID- 21576279 OWN - NLM STAT- MEDLINE DCOM- 20110929 LR - 20211020 IS - 1942-0080 (Electronic) IS - 1941-9651 (Print) IS - 1941-9651 (Linking) VI - 4 IP - 4 DP - 2011 Jul TI - Heterogeneity of intramural function in hypertrophic cardiomyopathy: mechanistic insights from MRI late gadolinium enhancement and high-resolution displacement encoding with stimulated echoes strain maps. PG - 425-34 LID - 10.1161/CIRCIMAGING.110.958751 [doi] AB - BACKGROUND: In hypertrophic cardiomyopathy (HCM), myocardial abnormalities are commonly heterogeneous. Two patterns of late gadolinium enhancement (LGE) have been reported: a bright "confluent" and an intermediate intensity abnormality termed "diffuse," each representing different degrees of myocardial scarring. We used MRI to study the relation between intramural cardiac function and the extent of fibrosis in HCM. The aim of this study was to determine whether excess collagen or myocardial scarring, as determined by LGE MRI, are the primary mechanisms leading to heterogeneous regional contractile function in patients with HCM. METHODS AND RESULTS: Intramural left ventricular strain, transmural left ventricular function, and regions of myocardial fibrosis/scarring were imaged in 22 patients with HCM, using displacement encoding with stimulated echoes (DENSE), cine MRI, and LGE. DENSE systolic strain maps were qualitatively and quantitatively compared with LGE images. Intramural systolic strain by DENSE was significantly depressed within areas of confluent and diffuse LGE but also in the core of the most hypertrophic nonenhanced segment (all P < 0.001 versus nonhypertrophied segments). DENSE demonstrated an unexpected inner rim of largely preserved contractile function and a noncontracting outer wall within hypertrophic segments in 91% of patients. CONCLUSIONS: LGE predicted some but not all of the heterogeneity of intramural contractile abnormalities. This indicates that myocardial scarring or excess interstitial collagen deposition does not fully explain the observed contractile heterogeneity in HCM. Thus, myofibril disarray or other nonfibrotic processes affect systolic function in a large number of patients with HCM. FAU - Aletras, Anthony H AU - Aletras AH AD - Cardiovascular and Pulmonary Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892-1061, USA. FAU - Tilak, Gauri S AU - Tilak GS FAU - Hsu, Li-Yueh AU - Hsu LY FAU - Arai, Andrew E AU - Arai AE LA - eng GR - ZIA HL004607-12/ImNIH/Intramural NIH HHS/United States GR - ZIA HL004607-14/ImNIH/Intramural NIH HHS/United States GR - ZID HL006140-01/ImNIH/Intramural NIH HHS/United States GR - ZIA HL004607-11/ImNIH/Intramural NIH HHS/United States GR - Z01 HL004607-10/ImNIH/Intramural NIH HHS/United States GR - Z01 HL004607-08 CE/CE/NCIPC CDC HHS/United States GR - Z01 HL004607-09/ImNIH/Intramural NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, N.I.H., Intramural DEP - 20110516 PL - United States TA - Circ Cardiovasc Imaging JT - Circulation. Cardiovascular imaging JID - 101479935 RN - 0 (Contrast Media) RN - K2I13DR72L (Gadolinium DTPA) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Cardiomyopathy, Hypertrophic/*physiopathology MH - Contrast Media MH - Echocardiography MH - Female MH - Gadolinium DTPA MH - Humans MH - Image Enhancement/methods MH - *Magnetic Resonance Imaging, Cine MH - Male MH - Middle Aged MH - Myocardial Contraction/physiology MH - Stroke Volume PMC - PMC3460377 MID - NIHMS305065 EDAT- 2011/05/18 06:00 MHDA- 2011/10/01 06:00 PMCR- 2012/09/28 CRDT- 2011/05/18 06:00 PHST- 2011/05/18 06:00 [entrez] PHST- 2011/05/18 06:00 [pubmed] PHST- 2011/10/01 06:00 [medline] PHST- 2012/09/28 00:00 [pmc-release] AID - CIRCIMAGING.110.958751 [pii] AID - 10.1161/CIRCIMAGING.110.958751 [doi] PST - ppublish SO - Circ Cardiovasc Imaging. 2011 Jul;4(4):425-34. doi: 10.1161/CIRCIMAGING.110.958751. Epub 2011 May 16.