Plasma Brain Natriuretic Peptide Levels Indicating Thromboembolism in Very Elderly Patients With Non-Valvular Atrial Fibrillation

Background Assessment of left atrial (LA) function by transesophageal echocardiography is useful for detecting patients with a high risk thromboembolism secondary to atrial fibrillation (AF). A recent study showed that the atrium is the main source of brain natriuretic peptide (BNP) in AF patients w...

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Veröffentlicht in:Circulation Journal 2007, Vol.71(9), pp.1446-1451
Hauptverfasser: Watanabe, Daisuke, Shizuka, Kazuhiko, Koyama, Shunichi, Iwamoto, Toshihiko
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Sprache:eng
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Zusammenfassung:Background Assessment of left atrial (LA) function by transesophageal echocardiography is useful for detecting patients with a high risk thromboembolism secondary to atrial fibrillation (AF). A recent study showed that the atrium is the main source of brain natriuretic peptide (BNP) in AF patients without overt heart failure. The purpose of this study was to assess the possible relationship between LA function and plasma BNP levels in very elderly patients with non-valvular AF. Methods and Results Seventy-four consecutive patients with chronic non-valvular AF (aged, 82±6 years) underwent transthoracic and transesophageal echocardiography and measurement of plasma BNP. Thirteen AF patients who had a history of cerebral embolism or echocardiographic evidence of thrombus (TE+ group) were compared with 61 AF patients who had no such complications (TE- group). The TE+ group demonstrated a lower LA appendage (LAA) velocity and higher plasma BNP level than the TE- group. Assessment of variables by multiple logistic regression analysis revealed that BNP was a significant predictor of thromboembolism. There was a significant negative correlation between the plasma BNP level and the LAA peak flow velocity. Conclusions The present findings would suggest the usefulness of measuring plasma BNP to detect very elderly non-valvular AF patients at high risk for thromboembolism. (Circ J 2007; 71: 1446 - 1451)
ISSN:1346-9843
1347-4820
DOI:10.1253/circj.71.1446