Role of natriuretic peptide to predict cardiac abnormalities in patients with hereditary transthyretin amyloidosis. (December 2013)
- Record Type:
- Journal Article
- Title:
- Role of natriuretic peptide to predict cardiac abnormalities in patients with hereditary transthyretin amyloidosis. (December 2013)
- Main Title:
- Role of natriuretic peptide to predict cardiac abnormalities in patients with hereditary transthyretin amyloidosis
- Authors:
- Damy, Thibaud
Deux, Jean-François
Moutereau, Stéphane
Guendouz, Soulef
Mohty, Dania
Rappeneau, Stéphane
Guellich, Aziz
Hittinger, Luc
Loric, Sylvain
Lefaucheur, Jean-Pascal
Plante-Bordeneuve, Violaine - Abstract:
- <abstract> <title>Abstract</title> <p> <italic>Background</italic>: Familial amyloid polyneuropathy (FAP) mainly targets the peripheral nervous system and heart. Early noninvasive detection of cardiac impairment is critical for therapeutic management.</p> <p> <italic>Aim</italic>: To assess if amino-terminal pro-brain natriuretic peptide (NT-proBNP) or troponin T (cTnT) can predict echocardiographic left-ventricle (LV) impairment in FAP.</p> <p> <italic>Methods</italic>: Thirty-six asymptomatic carriers and patients with FAP had echocardiographic measurement of left-ventricular (LV) systolic function, hypertrophy (LVH) and estimation of filling pressure (FP).</p> <p> <italic>Results</italic>: Overall, median age, NT-proBNP, and LV ejection fraction were, respectively, 59 years (41–74), 323 pg/ml (58–1960), and 60% (51–66). Twelve patients had increased cTnT. Prevalence of ATTR gene mutations was 53% for <italic>Val30Me</italic>t. Four individuals were asymptomatic, 6 patients had isolated neurological clinical signs, and 26 had echo-LV abnormalities. The ROC curve identified NT-proBNP patients with echo-LV abnormalities (area: 0.92; (0.83–0.99), <italic>p</italic> = 0.001) at a threshold &gt;82 pg/ml with a sensitivity of 92%, and a specificity of 90%. Increased in NT-proBNP occurred in patients with SD and/or LVH with or without increase in FP. Elevated cTnT (&gt;0.01ng/ml) was only observed in patients with LVH and systolic dysfunction, with or without FP.</p> <p><abstract> <title>Abstract</title> <p> <italic>Background</italic>: Familial amyloid polyneuropathy (FAP) mainly targets the peripheral nervous system and heart. Early noninvasive detection of cardiac impairment is critical for therapeutic management.</p> <p> <italic>Aim</italic>: To assess if amino-terminal pro-brain natriuretic peptide (NT-proBNP) or troponin T (cTnT) can predict echocardiographic left-ventricle (LV) impairment in FAP.</p> <p> <italic>Methods</italic>: Thirty-six asymptomatic carriers and patients with FAP had echocardiographic measurement of left-ventricular (LV) systolic function, hypertrophy (LVH) and estimation of filling pressure (FP).</p> <p> <italic>Results</italic>: Overall, median age, NT-proBNP, and LV ejection fraction were, respectively, 59 years (41–74), 323 pg/ml (58–1960), and 60% (51–66). Twelve patients had increased cTnT. Prevalence of ATTR gene mutations was 53% for <italic>Val30Me</italic>t. Four individuals were asymptomatic, 6 patients had isolated neurological clinical signs, and 26 had echo-LV abnormalities. The ROC curve identified NT-proBNP patients with echo-LV abnormalities (area: 0.92; (0.83–0.99), <italic>p</italic> = 0.001) at a threshold &gt;82 pg/ml with a sensitivity of 92%, and a specificity of 90%. Increased in NT-proBNP occurred in patients with SD and/or LVH with or without increase in FP. Elevated cTnT (&gt;0.01ng/ml) was only observed in patients with LVH and systolic dysfunction, with or without FP.</p> <p> <italic>Conclusion</italic>: In FAP, NT-proBNP was associated with cardiac impairment suggesting that NT-proBNP could be used in carriers or in FAP patients with only neurologic symptoms for identifying the appropriate time to start cardiac echocardiographic assessment and follow-up. cTnT identified patients with severe cardiac disease.</p> </abstract> … (more)
- Is Part Of:
- Amyloid. Volume 20:Number 4(2013:Dec.)
- Journal:
- Amyloid
- Issue:
- Volume 20:Number 4(2013:Dec.)
- Issue Display:
- Volume 20, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 20
- Issue:
- 4
- Issue Sort Value:
- 2013-0020-0004-0000
- Page Start:
- 212
- Page End:
- 220
- Publication Date:
- 2013-12
- Subjects:
- Amyloidosis -- Periodicals
616.3995 - Journal URLs:
- http://informahealthcare.com/loi/amy ↗
http://informahealthcare.com ↗ - DOI:
- 10.3109/13506129.2013.825240 ↗
- Languages:
- English
- ISSNs:
- 1350-6129
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0859.841173
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3855.xml