Evidence map›Paper›PMID 33277823›Full record

ArticleESC heart failure2021

Non-cardiac biopsy sites with high frequency of transthyretin amyloidosis.

Surendra Dasari, Angela Dispenzieri, Shareef Mansour, Prasuna Muppa, Paul J Kurtin, Jason D Theis, Julie A Vrana, Martha Grogan, Taxiarchis Kourelis, Morie A Gertz and 1 more

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Prostatic amyloidosis: pathological features of an underdiagnosed condition.Virchows Archiv : an international journal of pathology · 2025
    Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Surendra DasariDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Angela DispenzieriDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Shareef MansourDepartment of Medicine, Mayo Clinic, Rochester, MN, USA.
Prasuna MuppaDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Paul J KurtinDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Jason D TheisDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Julie A VranaDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Martha GroganDepartment of Medicine, Mayo Clinic, Rochester, MN, USA.
Taxiarchis KourelisDepartment of Medicine, Mayo Clinic, Rochester, MN, USA.
Morie A GertzDepartment of Medicine, Mayo Clinic, Rochester, MN, USA.
Ellen D McPhailDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0001-6918-3376
Mayo Clinic in Arizona · USMayo Clinic in Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsCardiac scintigraphy, a non-invasive technique for diagnosing ATTR cardiac amyloidosis, lacks specificity in patients with concomitant monoclonal gammopathy (up to 40% of cases). For these patients, amyloid type is often established by endomyocardial biopsy (EMB), which has clinical risk. This study aimed to investigate the frequency of ATTR in amyloid-positive tendon/synovium, urinary bladder, and prostate biopsies, sites for which prior biopsy specimens might exist for patients suspected of having cardiac amyloidosis, and, when available, determine the amyloid type concordance rate with other anatomic sites and provide clinical data regarding subsequent development of cardiac amyloidosis. METHODS AND

resultsWe queried our reference laboratory database of 19,298 amyloid specimens from myriad anatomic sites typed by mass spectrometry-based proteomics (LC-MS/MS) to investigate the frequency of ATTR amyloid in tendon/synovium, urinary bladder, and prostate. The amyloid type was ATTR in 104/138 (75.4%) tendon/synovium, 173/453 (38.0%) urinary bladder, and 27/81 (33.3%) prostate samples. Of 62 patients with available clinical data, 12 (19%) had bona fide ATTR cardiac amyloidosis prior to/concomitant with the non-cardiac site biopsy. Of the remaining 14 with follow-up, 8 developed bona fide and 2 probable cardiac amyloidosis; at last follow-up 4 had no evidence of cardiac amyloidosis. Fourteen of 16 patients (87.5%) for whom we typed both non-cardiac and cardiac sites had concordant amyloid types. There were 2 discordant cases (prostate = ASem1/heart = AL and urinary bladder = AL/heart = ATTR); only the latter is potentially clinically consequential.

conclusionsIn patients suspected of having cardiac amyloidosis based on cardiac scintigraphy, LC-MS/MS typing of Congophilic deposits in pre-existing biopsy specimens from non-cardiac sites may help establish the cardiac amyloid type, obviating the need for EMB. However, if the amyloid type identified in the non-cardiac site is not in keeping with other clinical features, then EMB for typing the cardiac amyloid might be indicated.

Indexed as

Amyloid Neuropathies, FamilialTandem Mass SpectrometryBiopsyChromatography, LiquidHumansMaleAmyloid typingATTRProstateSynoviumTendonUrinary bladder

Identifiers

PMID33277823
PMCPMC7835597
OpenAlexW3108137954

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.