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

被引:148
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
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