Concomitant Transthyretin Amyloidosis and Severe Aortic Stenosis in Elderly Indian Population A Pilot Study

被引:27
|
作者
Singal, Aayush Kumar [1 ]
Bansal, Raghav [1 ]
Singh, Avinainder [2 ]
Dorbala, Sharmila [3 ]
Sharma, Gautam [1 ]
Gupta, Kartik [4 ]
Saxena, Anita [1 ]
Bhargava, Balram [1 ,5 ,6 ]
Karthikeyan, Ganesan [1 ]
Ramakrishnan, Sivasubramanian [1 ]
Bisoi, Akshay Kumar [7 ]
Hote, Milind Padmakar [7 ]
Rajashekar, Palleti [7 ]
Chowdhury, Ujjwal Kumar [7 ]
Devagourou, Velayoudam [7 ]
Patel, Chetan [8 ]
Ray, Ruma [9 ]
Arawa, Sudheer Kumar [9 ]
Mishra, Sundeep [1 ]
机构
[1] AIIMS, Dept Cardiol, New Delhi, India
[2] Yale Sch Med, Dept Internal Med, New Haven, CT USA
[3] Brigham & Womens Hosp, Dept Radiol, 75 Francis St, Boston, MA 02115 USA
[4] Henry Ford Hosp, Dept Med, Detroit, MI 48202 USA
[5] Indian Council Med Res, New Delhi, India
[6] Govt India, Dept Hlth Res, Minist Hlth & Family Welf, New Delhi, India
[7] AIIMS, Dept CTVS, New Delhi, India
[8] AIIMS, Dept Nucl Med, New Delhi, India
[9] AIIMS, Dept Pathol, New Delhi, India
来源
JACC: CARDIOONCOLOGY | 2021年 / 3卷 / 04期
关键词
dual aortic stenosis transthyretin cardiac amyloidosis; severe aortic stenosis;   transthyretin cardiac amyloidosis; 99m-technetium pyrophosphate scan; CARDIAC AMYLOIDOSIS; PATHOLOGY;
D O I
10.1016/j.jaccao.2021.08.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND Prevalence of both degenerative severe aortic stenosis (AS) and transthyretin cardiac amyloidosis (ATTR-CA) increases with age. Dual disease (AS+myocardial ATTR-CA) occurs in significant proportion of patients undergoing surgical aortic valve replacement (SAVR). OBJECTIVES This study aimed to determine the prevalence of ATTR-CA in severe AS in the Indian population, identify noninvasive predictors of its diagnosis, and understand its impact on prognosis. METHODS Symptomatic severe AS patients aged $65 years undergoing SAVR were enrolled. ATTR-CA diagnosis was based on preoperative 99m-technetium pyrophosphate (PYP) scan and intraoperatively obtained basal interventricular septum biopsy for myocardial ATTR-CA, and excised native aortic valve for isolated valvular ATTR-CA. Primary amyloidosis was excluded by serum/urine protein electrophoresis with serum immunofixation. RESULTS SAVR was performed in 46 AS patients (age 70 +/- 5 years, 70% men). PYP scan was performed for 32 patients, with significant PYP uptake in 3 (n = 3 of 32, 9.4%), suggestive of myocardial ATTR-CA. On histopathological examination, none of the interventricular septum biopsy specimens had amyloid deposits, whereas 33 (71.7%) native aortic valves showed amyloid deposits, of which 19 (57.6%) had transthyretin deposition suggestive of isolated valvular amyloidosis. Noninvasive markers of dual disease included low myocardial contraction fraction (median [interquartile range], 28.8% [23.8% to 39.1%] vs 15.3% [9.3% to 16.1%]; P = 0.006), deceleration time (215 [144 to 236] ms vs 88 [60 to 106] ms; P = 0.009) and global longitudinal strain (-18.7% [-21.1% to-16.9%] vs-14.2% [-17.0% to-9.7%]; P = 0.030). At 1-year follow-up, 2 patients died (4.3%); 1 each in myocardial ATTR-CA negative and positive groups (3.4% vs 33.3%; P = 0.477). CONCLUSIONS Dual disease is not uncommon in India. Isolated valvular amyloidosis in severe AS is much more common.
引用
收藏
页码:565 / 576
页数:12
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