Evidence map›Paper›PMID 35754288›Full record

ArticleJournal of Parkinson's disease2022

Progressive Olfactory Impairment and Cardiac Sympathetic Denervation in REM Sleep Behavior Disorder.

Annette Janzen, David Vadasz, Jan Booij, Markus Luster, Damiano Librizzi, Martin T Henrich, Lars Timmermann, Mahboubeh Habibi, Elisabeth Sittig, Geert Mayer and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of Parkinson's disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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  8. Reduced cardiacBrain communications · 2024
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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

12 authors at 2 institutions in 2 countries.

Annette JanzenDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
David VadaszDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Jan BooijDepartment of Radiology and Nuclear Medicine, Amsterdam UMC, location Academic Medical Center Amsterdam, Amsterdam, The Netherlands.
Markus LusterDepartment of Nuclear Medicine, Philipps-University Marburg, Marburg, Germany.
Damiano LibrizziDepartment of Nuclear Medicine, Philipps-University Marburg, Marburg, Germany.
Martin T HenrichDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Lars TimmermannDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Mahboubeh HabibiDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Elisabeth SittigDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Geert MayerDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Fanni GeiblDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Wolfgang OertelDepartment of Neurology, Philipps-University Marburg, Marburg, Germany.
Philipps University of Marburg · DEAcademic Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIsolated rapid eye movement sleep behavior disorder (iRBD) is prodromal for Parkinson's disease (PD) and dementia with Lewy bodies (DLB).

objectiveWe investigated the use of cardiac [123I]meta-iodo-benzyl-guanidine scintigraphy ([123I]MIBG) and olfactory testing- in comparison to [123I]N-ω-fluoropropyl-2β-carbomethoxy-3β-(4-iodophenyl)nortropane single photon emission computed tomography ([123I]FP-CIT-SPECT)- for identifying iRBD patients as prodromal phenotype of PD/DLB.

methods37 RBD subjects underwent cardiac [123I]MIBG and brain [123I]FP-CIT-SPECT at baseline. Olfactory (Sniffin' Sticks), cognitive and motor functions were tested annually for ∼4 years.

results29/37 (78.4%) subjects had a pathological [123I]MIBG, of whom 86.2% (25/29) presented at least a moderate hyposmia at baseline (threshold/discrimination/identification-(TDI-)score ≤25). 20/37 (54.1%) subjects had a pathological [123I]FP-CIT-SPECT, always combined with a pathological [123I]MIBG. In subjects with pathological [123I]MIBG, olfactory function worsened (mainly due to threshold and discrimination subscores) from baseline to follow-up (p = 0.005). Olfaction was more impaired in subjects with pathological [123I]MIBG compared to those with normal [123I]MIBG at baseline (p = 0.001) and follow-up (p < 0.001). UPDRS-III scores increased in subjects with both pathological [123I]MIBG and [123I]FP-CIT-SPECT. In this group, seven subjects phenoconverted to PD, all- except for one- presented with at least moderate hyposmia at baseline.

conclusionA combination of the biomarkers "pathological [123I]MIBG" and "hyposmia" likely identifies iRBD patients in an early prodromal stage of PD/DLB, i.e., before nigrostriatal degeneration is visualized. One-third of the subjects with pathological [123I]MIBG had a normal [123I]FP-CIT-SPECT. Noteworthy, in iRBD subjects with pathological [123I]MIBG, olfactory impairment is progressive independent of the [123I]FP-CIT-SPECT status.

Indexed as

Lewy Body DiseaseOlfaction DisordersParkinson DiseaseREM Sleep Behavior Disorder3-IodobenzylguanidineHumansSympathectomyTomography, Emission-Computed, Single-PhotonTropanes3-IodobenzylguanidineTropanes[123I]FP-CIT-SPECTBiomarkercardiac [123I]MIBG scintigraphyhyposmiaisolated rapid eye movement sleep behavior disorderprodromal progression marker

Identifiers

PMID35754288
PMCPMC9535565
OpenAlexW4283381651

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.