Evidence map›Paper›PMID 34543661›Full record

ArticleAmerican journal of ophthalmology2022

Longitudinal Associations Between Vision Impairment and the Incidence of Neuropsychiatric, Musculoskeletal, and Cardiometabolic Chronic Diseases.

Ajay Kolli, Kristian Seiler, Neil Kamdar, Lindsey B De Lott, Mark D Peterson, Michelle A Meade, Joshua R Ehrlich

Abstract read
In one paragraph

Article in American journal of ophthalmology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

7 authors.

Ajay KolliFrom the University of Michigan Medical School, University of Michigan (A.K.), Ann Arbor, Michigan; Harvard T.H. Chan School of Public Health, Harvard University (A.K.), Boston, Massachusetts.
Kristian SeilerInstitute for Healthcare Policy and Innovation, University of Michigan (K.S., N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), Ann Arbor, Michigan.
Neil KamdarInstitute for Healthcare Policy and Innovation, University of Michigan (K.S., N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), Ann Arbor, Michigan; University of Michigan Center for Disability Health and Wellness (N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), University of Michigan, Ann Arbor, Michigan; Department of Surgery, Michigan Medicine, University of Michigan (N.K.), Ann Arbor, Michigan; Department of Obstetrics and Gynecology, Michigan Medicine, University of Michigan (N.K.), Ann Arbor, Michigan.
Lindsey B De LottInstitute for Healthcare Policy and Innovation, University of Michigan (K.S., N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), Ann Arbor, Michigan; University of Michigan Center for Disability Health and Wellness (N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), University of Michigan, Ann Arbor, Michigan; Department of Ophthalmology & Visual Sciences, Michigan Medicine (L.B.D.L., J.R.E.), Ann Arbor, Michigan.
Mark D PetersonInstitute for Healthcare Policy and Innovation, University of Michigan (K.S., N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), Ann Arbor, Michigan; University of Michigan Center for Disability Health and Wellness (N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), University of Michigan, Ann Arbor, Michigan; Department of Physical Medicine and Rehabilitation, Michigan Medicine, University of Michigan (M.D.P., M.A.M.), Ann Arbor, Michigan, USA.
Michelle A MeadeInstitute for Healthcare Policy and Innovation, University of Michigan (K.S., N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), Ann Arbor, Michigan; University of Michigan Center for Disability Health and Wellness (N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), University of Michigan, Ann Arbor, Michigan; Department of Physical Medicine and Rehabilitation, Michigan Medicine, University of Michigan (M.D.P., M.A.M.), Ann Arbor, Michigan, USA.
Joshua R EhrlichInstitute for Healthcare Policy and Innovation, University of Michigan (K.S., N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), Ann Arbor, Michigan; University of Michigan Center for Disability Health and Wellness (N.K., L.B.D.L., M.D.P., M.A.M., J.R.E.), University of Michigan, Ann Arbor, Michigan; Department of Ophthalmology & Visual Sciences, Michigan Medicine (L.B.D.L., J.R.E.), Ann Arbor, Michigan; Institute for Social Research, University of Michigan, Ann Arbor, Michigan. Electronic address: joshre@med.umich.edu.

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Addressing Low Vision due to Severe Peripheral Field Loss: Development and Validation of a Patient-Centered Outcome MeasureK23EY027848 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI EHRLICH, JOSHUA ROBERT · 2017 to 2021
$1.2M
Optimizing Treatment Decisions for Acute Demyelinating Optic NeuritisK23EY027849 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DE LOTT, LINDSEY BLAKE · 2018 to 2022
$1.0M
NCATS NIH HHS UL1 TR002240NEI NIH HHS K23 EY027848NEI NIH HHS K23 EY027849
6 · The paper itself

Abstract

purposeTo compare the incidence and hazard of neuropsychiatric, musculoskeletal, and cardiometabolic conditions among adults with and without vision impairment (VI).

designRetrospective cohort study.

methodsThe sample comprised enrollees in a large private health insurance provider in the United States, including 24 657 adults aged ≥18 years with VI and age- and sex-matched controls. The exposure variable, VI, was based on low vision and blindness International Classification of Diseases, Ninth and Tenth Revision, Clinical Modification (ICD-9-CM and ICD-10-CM), diagnosis codes. Physician-diagnosed incident neuropsychiatric, musculoskeletal, and cardiometabolic diseases were identified using ICD codes. Separate Cox proportional hazards regression models were used to assess the association of VI with incidence of 30 chronic conditions, adjusting for Elixhauser Comorbidity Index. Analyses were stratified by age 18-64 years and ≥65 years.

resultsIn individuals with VI aged 18-64 years (n=7478), the adjusted hazard of neuropsychiatric (HR 2.1, 95% CI 1.9, 2.4), musculoskeletal (HR 1.8, 95% CI 1.7, 2.0), and cardiometabolic (HR 1.8, 95% CI 1.7, 2.0) diseases was significantly greater than in matched controls (mean 5.5 years follow-up). Similar associations were seen between patients with VI aged ≥65 years (n=17 179) for neuropsychiatric (HR 2.4, 95% CI 2.1, 2.7), musculoskeletal (HR 1.8, 95% CI 1.6, 1.9), and cardiometabolic (HR 1.7, 95% CI 1.4, 2.0) diseases. VI was associated with a higher hazard of each of the 30 conditions we assessed, with similar results in both age cohorts.

conclusionAcross the life span, adults with VI had an approximately 2-fold greater adjusted hazard for common neuropsychiatric, musculoskeletal, and cardiometabolic disorders compared with matched controls without VI.

Indexed as

Cardiovascular DiseasesAdolescentAdultAgedChronic DiseaseHumansIncidenceMiddle AgedProportional Hazards ModelsRetrospective StudiesRisk FactorsUnited StatesYoung Adult

Identifiers

PMID34543661
PMCPMC8863581

What OpenQuestion holds

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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.