Evidence map›Paper›PMID 40406818›Full record

SynthesisJournal of inherited metabolic disease2025

Diagnosis of Inherited Metabolic Disease in Older Patients: A Systematic Literature Review.

Maria-Rita Moio, Julia Cordeiro Milke, Yannick Moutapam-Ngamby-Adriaansen, Arthur Minas Alberti, Marie Gernay, Eduardo Augusto Schütz, Ida Vanessa Doederlein Schwartz, François Maillot

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of inherited metabolic disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
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

8 authors.

Maria-Rita MoioDepartment of Internal Medicine, University Hospital of Tours, Tours, France.
Julia Cordeiro MilkeMedicine School, Federal University of Rio Grande Do Sul, Porto Alegre, Brazil.
Yannick Moutapam-Ngamby-AdriaansenDepartment of Internal Medicine, University Hospital of Tours, Tours, France.
Arthur Minas AlbertiMedicine School, Federal University of Health Sciences, Porto Alegre, Brazil.
Marie GernayDivision of Diabetes, Nutrition and Metabolic Diseases, Department of Medicine, University Hospital of Liege, Liege, Belgium.
Eduardo Augusto SchützNuclimed, Clinical Research Center, Hospital de Clinicas de Porto Alegre, Brazil.
Ida Vanessa Doederlein SchwartzNuclimed, Clinical Research Center, Hospital de Clinicas de Porto Alegre, Brazil.
François MaillotDepartment of Internal Medicine, University Hospital of Tours, Tours, France.ORCID 0000-0002-1979-5769

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited metabolic diseases (IMDs) are genetic disorders that disrupt biochemical processes in the human body, due to pathogenic variants in genes encoding enzymes or transporters. While IMDs are mostly diagnosed in infancy or childhood, there is an increasing number of diagnoses in adult patients. Delayed diagnosis, particularly in older patients, may reflect the diagnostic odyssey usually observed in rare diseases' patients and can result in complications and reduced quality of life for patients and their families. The aim of the study was to better characterize the diagnosis of IMDs in older patients (≥ 65 years). We conducted a systematic literature review (SLR) to examine the diagnosis and clinical presentation of IMDs in patients aged 65 and older. We searched databases like PubMed, Embase, and Lilacs for relevant studies from 1965 to 2023. A total of 260 articles were included, representing 293 patients with a median age of 69 years at diagnosis. From this SLR, 67 different diagnoses have been reported. The most frequently reported diseases were Fabry disease, alkaptonuria, Gaucher disease, mitochondrial disorders, and glycogen storage disease type V. Median diagnostic delay was 14.5 years with a wide range of 1-91 years. Musculoskeletal symptoms were the most frequently reported, followed by neurological and cardiovascular symptoms. Our findings underscore the importance of recognizing IMDs in older patients and the need for awareness among healthcare providers to improve diagnosis and patient care. Future guidelines and teaching programs should incorporate metabolic investigations for older patients presenting with symptoms suggestive of IMDs.

Indexed as

Metabolic DiseasesMetabolism, Inborn ErrorsAgedAged, 80 and overDelayed DiagnosisFemaleHumansMaleQuality of Lifeadult metabolic medicineelderlyinborn errors of metabolisminherited metabolic diseaseolder patients

Identifiers

PMID40406818
PMCPMC12100460

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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.