Evidence map›Paper›PMID 29479262›Full record

ArticlePaediatrics & child health2017

Increasing incidence of optic nerve hypoplasia/septo-optic dysplasia spectrum: Geographic clustering in Northern Canada.

Tanya Khaper, Martin Bunge, Ian Clark, Mubeen Fatima Rafay, Aziz Mhanni, Nicole Kirouac, Atul Sharma, Celia Rodd, Brandy Wicklow

Abstract read
In one paragraph

Article in Paediatrics & child health, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Septo-Optic Dysplasia: A Case Series of 33 Patients.Neuro-ophthalmology (Aeolus Press) · 2024
    Article
  4. Article
  5. Hypothalamic syndrome.Nature reviews. Disease primers · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Non-Cell Autonomous Roles for CASK in Optic Nerve Hypoplasia.Investigative ophthalmology & visual science · 2019
    Article
  11. Review
  12. Article
  13. 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

9 authors.

Tanya KhaperRady College of Medicine, University of Manitoba, Winnipeg, Manitoba.
Martin BungeSection of Pediatric Radiology, Children's Hospital of Winnipeg, University of Manitoba, Winnipeg, Manitoba.
Ian ClarkSection of Pediatric Ophthalmology, Children's Hospital of Winnipeg, University of Manitoba, Winnipeg, Manitoba.
Mubeen Fatima RafaySection of Pediatric Neurology, Department of Pediatrics and Child Health, Children's Hospital of Winnipeg, University of Manitoba, Winnipeg, Manitoba.
Aziz MhanniDepartment of Biochemistry & Medical Genetics, Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba.
Nicole KirouacSection of Pediatric Endocrinology, Children's Hospital Winnipeg, University of Manitoba, Winnipeg, Manitoba.
Atul SharmaGeorge and Fay Yee Center for Healthcare Innovation, University of Manitoba, Winnipeg, Manitoba.
Celia RoddSection of Pediatric Endocrinology, Children's Hospital Winnipeg, University of Manitoba, Winnipeg, Manitoba.
Brandy WicklowSection of Pediatric Endocrinology, Children's Hospital Winnipeg, University of Manitoba, Winnipeg, Manitoba.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOwing to the shared embryonic origin, defects in development of optic nerves are often seen in conjunction with defects affecting the surrounding brain and pituitary gland. Optic nerve hypoplasia (ONH) and septo-optic dysplasia (SOD) represent a clinical spectrum associated with visual, pituitary and severe central nervous system structural abnormalities (SODplus). Based on changing clinical patterns, our primary objective was to examine trends in annual incidence of ONH/SOD and geographical clustering in Manitoba.

methodsThis was a retrospective 1996 to 2015 chart review with extraction of anthropometric measures, radiologic findings, parental characteristics, endocrinopathies and neurologic symptoms from all involved in care. Postal codes were used to assign map co-ordinates and identify relevant census-based deprivation indices.

resultsNinety-three children were identified in our catchment area; Poisson regression confirmed a striking 1.11-fold annual increase (95% confidence interval 1.07 to 1.16) or ~800% over two decades. The annual incidence (averaged 2010 to 2014 chart data) reached 53.3 per 100,000, affecting 1 in 1875 live births. Most (~55%) had SODplus. Common presenting features were hypoglycemia, nystagmus, seizures and developmental delay; 40% had hormone deficiencies; 80% had reduced visual acuity, typically bilateral. Many were premature with young, primiparous mothers. Unhealthy maternal lifestyles and severe material deprivation were noted. There was disproportionate clustering in individuals from Northern Manitoba at three times the average provincial rate.

conclusionWe noted a dramatic rise in the annual incidence of ONH/SOD, which was strongly associated with poverty and northern communities. The pattern was consistent with environmental or nutritional etiologies. Many children were severely affected with increased morbidity and health care burdens.

Indexed as

BlindnessHypopituitarismIncidencePovertySepto-optic dysplasia

Identifiers

PMID29479262
PMCPMC5804768

What OpenQuestion holds

Textmetadata
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.