Use of Serum Transthyretin as a Prognostic Indicator and Predictor of Outcome in Cardiac Amyloid Disease Associated With Wild-Type Transthyretin

被引:59
|
作者
Hanson, Jacquelyn L. S. [1 ,2 ]
Arvanitis, Marios [3 ]
Koch, Clarissa M. [1 ,2 ]
Berk, John L. [1 ,3 ]
Ruberg, Frederick L. [1 ,3 ,4 ]
Prokaeva, Tatiana [1 ]
Connors, Lawreen H. [1 ,2 ]
机构
[1] Boston Univ, Sch Med, Amyloidosis Ctr, 72 East Concord St,K508, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Pathol & Lab Med, 72 East Concord St,K508, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Dept Med, 72 East Concord St,K508, Boston, MA 02118 USA
[4] Boston Univ, Sch Med, Dept Med, Sect Cardiovasc Med, 72 East Concord St,K508, Boston, MA 02118 USA
基金
美国国家卫生研究院;
关键词
amyloid; biomarker; heart failure; risk factor; survival; PREALBUMIN; POLYNEUROPATHY;
D O I
10.1161/CIRCHEARTFAILURE.117.004000
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Wild-type transthyretin amyloidosis (ATTRwt), an underappreciated cause of heart failure in older adults, is challenging to diagnose and monitor in the absence of validated, disease-specific biomarkers. We examined the prognostic use and survival association of serum TTR (transthyretin) concentration in ATTRwt. METHODS AND RESULTS: Patients with biopsy-proven ATTRwt were retrospectively identified. Serum TTR, cardiac biomarkers, and echocardiographic parameters were assessed at baseline and follow-up evaluations. Statistical analyses included Kaplan-Meier method, Cox proportional hazard survival models, and receiver-operating characteristic curve analysis. Median serum TTR concentration at presentation was 23 mg/dL (n=116). Multivariate predictors of shorter overall survival were decreased TTR, left ventricular ejection fraction and elevated cTn-I (cardiac troponin I); an inclusive model demonstrated superior accuracy in 4-year survival prediction by receiver-operating characteristic curve analysis (area under the curve, 0.77). TTR values lower than the normal limit, < 18 mg/dL, were associated with shorter survival (2.8 versus 4.1 years; P=0.03). Further, TTR values at 1- and 2-year follow-ups were significantly lower (P<0.001) in untreated patients (n=23) compared with those treated with TTR stabilizer, diflunisal (n=12), after baseline evaluation. During 2-year follow-up, unchanged TTR corresponded to increased cTn-I (P=0.006) in untreated patients; conversely, the diflunisal-treated group showed increased TTR (P=0.001) and stabilized cTn-I and left ventricular ejection fraction at 1 year. CONCLUSIONS: In this series of biopsy-proven ATTRwt, lower baseline serum TTR concentration was associated with shorter survival as an independent predictor of outcome. Longitudinal analysis demonstrated that decreasing TTR corresponded to worsening cardiac function. These data suggest that TTR may be a useful prognostic marker and predictor of outcome in ATTRwt.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Acute aortic dissection associated with wild-type transthyretin amyloid
    Mori, Shinichiro
    Hatae, Ryusuke
    Iwaki, Toru
    PATHOLOGY INTERNATIONAL, 2021, 71 (08) : 556 - 558
  • [2] Assessment of transthyretin instability in patients with wild-type transthyretin amyloid cardiomyopathy
    Iino, Takuya
    Nagao, Manabu
    Tanaka, Hidekazu
    Yoshikawa, Sachiko
    Asakura, Junko
    Nishimori, Makoto
    Shinohara, Masakazu
    Harada, Amane
    Watanabe, Shunsuke
    Ishida, Tatsuro
    Hirata, Ken-ichi
    Toh, Ryuji
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [3] AMYLOID POLYNEUROPATHY CAUSED BY WILD-TYPE TRANSTHYRETIN
    Lam, Lynda
    Margeta, Marta
    Layzer, Robert
    MUSCLE & NERVE, 2015, 52 (01) : 146 - 149
  • [4] Differential Association of Transthyretin Stability with Variant and Wild-Type Transthyretin Amyloid Cardiomyopathy
    Urina-Jassir, Manuel
    Teruya, Sergio
    Blaner, William S.
    Brun, Pierre-Jacques
    Prokaeva, Tatiana
    Tsai, Felix J.
    Kelly, Jeffery W.
    Maurer, Mathew S.
    Ruberg, Frederick L.
    JACC-HEART FAILURE, 2024, 12 (12) : 2113 - 2115
  • [5] Prognostic factors associated with survival in patients with wild-type transthyretin amyloid cardiomyopathy, treated with tafamidis
    Zemljic, G.
    Frljak, S.
    Poglajen, G.
    Zorz, N.
    Cerar, A.
    Okrajsek, R.
    Bajec, T.
    Vrtovec, B.
    EUROPEAN JOURNAL OF HEART FAILURE, 2024, 26 : 162 - 162
  • [6] Cardiac amyloid in patients with familial amyloid polyneuropathy consists of abundant wild-type transthyretin
    Yazaki, M
    Tokuda, T
    Nakamura, A
    Higashikata, T
    Koyama, J
    Higuchi, K
    Harihara, Y
    Baba, S
    Kametani, F
    Ikeda, S
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 274 (03) : 702 - 706
  • [7] Early Diagnosis and Outcome in Patients With Wild-Type Transthyretin Cardiac Amyloidosis
    Fumagalli, Carlo
    Zampieri, Mattia
    Perfetto, Federico
    Zocchi, Chiara
    Maurizi, Niccolo
    Tassetti, Luigi
    Ungar, Andrea
    Gabriele, Martina
    Nardi, Giulia
    Del Monaco, Guido
    Baldini, Katia
    Tomberli, Alessia
    Tomberli, Benedetta
    Marchionni, Niccolo
    Di Mario, Carlo
    Olivotto, Iacopo
    Cappelli, Francesco
    MAYO CLINIC PROCEEDINGS, 2021, 96 (08) : 2185 - 2191
  • [8] Progress in Cardiac Imaging Uncovers the Epidemiology of Wild-Type Transthyretin Amyloid Cardiomyopathy
    Dorbala, Sharmila
    Clerc, Olivier Florian
    JACC: CARDIOONCOLOGY, 2021, 3 (04): : 547 - 549
  • [9] Temporal Trends of Wild-Type Transthyretin Amyloid Cardiomyopathy in the Transthyretin Amyloidosis Outcomes Survey
    Nativi-Nicolau, Jose
    Siu, Alfonso
    Dispenzieri, Angela
    Maurer, Mathew S.
    Rapezzi, Claudio
    Kristen, Arnt, V
    Garcia-Pavia, Pablo
    LoRusso, Samantha
    Waddington-Cruz, Marcia
    Lairez, Olivier
    Witteles, Ronald
    Chapman, Doug
    Amass, Leslie
    Grogan, Martha
    JACC: CARDIOONCOLOGY, 2021, 3 (04): : 537 - 546
  • [10] Correlation Between Cardiac Images, Biomarkers, and Amyloid Load in Wild-Type Transthyretin Amyloid Cardiomyopathy
    Morioka, Mami
    Takashio, Seiji
    Nakashima, Naoya
    Nishi, Masato
    Fujiyama, Akira
    Hirakawa, Kyoko
    Hanatani, Shinsuke
    Usuku, Hiroki
    Yamamoto, Eiichiro
    Kidoh, Masafumi
    Oda, Seitaro
    Matsushita, Kenichi
    Ueda, Mitsuharu
    Tsujita, Kenichi
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2022, 11 (12):