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
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS | 2016年 / 23卷 / 01期
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 33 条
  • [31] Systemic low-grade C-reactive protein is associated with proximal symptom spread in carpal tunnel syndrome
    Zvonickova, Karolina
    Rhee, Amber
    Sandy-Hindmarch, Oliver
    Furniss, Dominic
    Wiberg, Akira
    Schmid, Annina B.
    PAIN REPORTS, 2024, 9 (03) : E1156
  • [32] Unusual hypertrophic cardiomyopathy: case report of an early onset wild-type ATTR amyloidosis accompanied by a chromosomal duplication involving the MYH6 and MYH7 gene
    Hamidi, Jassin
    Hanel, Yvonne
    Dittmann, Sven
    Gerding, Wanda Maria
    Nguyen, Huu Phuc
    Klingel, Karin
    Schulze-Bahr, Eric
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2025, 12
  • [33] Where Neurosurgery Meets Heart Failure: A Case Report of a Patient with Amyloid Transthyretin Wild Type in the Ligamentum Flavum and Cardiac Tissue with Bilateral Carpal Tunnel Syndrome
    Dowd, Richard S.
    Nail, T. Jayde
    Arkun, Knarik
    Kryzanski, James
    Soto, Oscar
    Fogaren, Teresa
    Harrington, Kelly
    Patel, Ayan
    Comenzo, Raymond
    Riesenburger, Ron, I
    WORLD NEUROSURGERY, 2019, 131 : 104 - 107