Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis

被引:140
|
作者
Nakagawa, Michitaka [1 ]
Sekijima, Yoshiki [1 ,2 ]
Yazaki, Masahide [1 ,2 ]
Tojo, Kana [1 ]
Yoshinaga, Tsuneaki [1 ]
Doden, Tadashi [1 ]
Koyama, Jun [3 ]
Yanagisawa, Shin [4 ]
Ikeda, Shu-Ichi [1 ,2 ]
机构
[1] Shinshu Univ, Sch Med, Dept Med Neurol & Rheumatol, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Inst Biomed Sci, Matsumoto, Nagano 3908621, Japan
[3] Shinshu Univ, Sch Med, Dept Cardiovasc Med, Matsumoto, Nagano 3908621, Japan
[4] Shinshu Univ, Sch Med, Dept Radiol, Matsumoto, Nagano 3908621, Japan
来源
关键词
Amyloid; transthyretin; carpal tunnel syndrome; senile systemic amyloidosis; wild-type ATTR (ATTRwt) amyloidosis; BILATERAL CARPAL; CARDIAC AMYLOIDOSIS; TRANSTHYRETIN; DEPOSITION; POLYNEUROPATHY; PREVALENCE; BIOPSY;
D O I
10.3109/13506129.2015.1135792
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Systemic wild-type ATTR (ATTRwt) amyloidosis is a prevalent aging-related disorder. However, a limited number of systemic ATTRwt amyloidosis patients have been diagnosed antemortem, and therefore, the prevalence of ATTRwt is underestimated. Here, we investigated clinical findings of a series of systemic ATTRwt amyloidosis patients with antemortem diagnosis. Methods: Thirty-one consecutive patients diagnosed with systemic ATTRwt amyloidosis at Shinshu University Hospital were included in this study. Systemic ATTRwt amyloidosis was diagnosed based on proven ATTR amyloid deposition in biopsy specimens and confirmation of wild-type TTR genotype. Results: The systemic ATTRwt amyloidosis patients consisted of 24 men and seven women, and mean age of onset was 69.8 +/- 9.0 years. The most common initial symptom was carpal tunnel syndrome (CTS, 17 patients), followed by heart failure symptoms (14 patients). The mean age at diagnosis was 74.5 +/- 8.3 years and the duration of illness from onset to diagnosis was 5.4 +/- 4.4 years. Cardiogenic embolism and renal dysfunction are also frequently seen during the course of the disease. Conclusions: CTS is the most common initial symptom of systemic ATTRwt amyloidosis. Our results suggest the possibility of systemic ATTRwt amyloidosis diagnosis at an early stage by carefully examining patients with CTS.
引用
收藏
页码:58 / 63
页数:6
相关论文
共 50 条
  • [41] Amyloid detection in the transverse carpal ligament of patients with hereditary ATTR V30M amyloidosis and carpal tunnel syndrome
    Samoes, Raquel
    Taipa, Ricardo
    Valdrez, Katia
    Goncalves, Isabel
    Pires, Manuel Melo
    da Silva, Ana Martins
    Coelho, Teresa
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2017, 24 (02): : 73 - 77
  • [42] Carpal tunnel syndrome, spinal canal stenosis, cardiomyopathy, renal insufficiency, enteropathy, and diffuse myopathy as an expression of systemic ATTR amyloidosis - diagnostics and therapy
    Radmer, Sebastian
    Andresen, Julian Ramin
    JOURNAL OF SURGICAL CASE REPORTS, 2024, 2024 (03):
  • [43] A descriptive analysis of patients with wild-type ATTR cardiomyopathy from the transthyretin amyloidosis outcomes survey
    Garcia-Pavia, P.
    Grogan, M.
    Dispenzieri, A.
    Mundayat, R.
    Amass, L.
    Rapezzi, C.
    EUROPEAN HEART JOURNAL, 2019, 40 : 133 - 133
  • [44] Diagnosing Systemic Amyloidosis Presenting as Carpal Tunnel Syndrome A Risk Nomogram to Guide Biopsy at Time of Carpal Tunnel Release
    Sood, Ravi F.
    Kamenko, Srdjan
    McCreary, Eleanor
    Sather, Bergen K.
    Schmitt, Michael
    Peterson, Steven L.
    Lipira, Angelo B.
    JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2021, 103 (14): : 1284 - 1294
  • [45] Senile systemic amyloidosis starting as bilateral carpal and left ulnar tunnel syndrome
    Takei, Y
    Hattori, T
    Tokuda, T
    Matsuda, M
    Saitoh, S
    Hoshii, Y
    Ikeda, S
    INTERNAL MEDICINE, 2003, 42 (10) : 1050 - 1051
  • [46] Cardiac transthyretin wild-type amyloidosis (ATTRwt): a prospective study of 400 patients followed at the Italian referral center
    Milani, P.
    Obici, L.
    Mussinelli, R.
    Basset, M.
    Manfrinato, G.
    Nuvolone, M.
    De Matteis, G.
    Sabena, A.
    Benigna, F.
    Cavenaghi, G.
    Foli, A.
    Perlini, S.
    Merlini, G.
    Palladini, G.
    EUROPEAN HEART JOURNAL, 2020, 41 : 2144 - 2144
  • [47] Progressive Hereditary Transthyretin-Related Amyloidosis (ATTRv) Aggravated by ATTR Wild-Type and Complement Activation
    Mattig, Isabel
    Heidecker, Bettina
    Tschoepe, Carsten
    Messroghli, Daniel
    Eurich, Dennis
    Kleefeld, Felix
    Gaedeke, Jens
    Stenzel, Werner
    Schmidt, Hartmut H. -J
    Roecken, Christoph
    Knebel, Fabian
    Hahn, Katrin
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2022, 81 (04): : 299 - 303
  • [48] Identifying and tracking the evolution of wild-type transthyretin (ATTR-wt) amyloidosis in extracardiac tissues/organs
    Staron, Andrew
    Ruberg, Frederick
    Siddiqi, Omar K.
    Gopal, Deepa M.
    Mendelson, Lisa
    Joshi, Tracy
    Burke, Natasha
    Berk, John L.
    Sanchorawala, Vaishali
    AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, 2024, 31 : S85 - S85
  • [49] Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA), previously known as senile cardiac amyloidosis: clinical presentation, diagnosis, management and emerging therapies
    Halatchev, Ilia G.
    Zheng, Jingsheng
    Ou, Jiafu
    JOURNAL OF THORACIC DISEASE, 2018, 10 (03) : 2034 - 2045
  • [50] Spontaneous Retropharyngeal And Mediastinal Hemorrhage Associated With Wild-Type Transthyretin Systemic Amyloidosis
    Cummings, M. J.
    Katz, S. E.
    De Gonzalez, A. Koehne
    Darmanian, A. C.
    O'Donnell, M. R.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 191