Evidence map›Paper›PMID 40492460›Full record

ArticleEpilepsia open2025

Rest-activity rhythm phenotypes in adults with epilepsy and intellectual disability.

Nandani Adhyapak, Grace E Cardenas, Mark A Abboud, Vaishnav Krishnan

Abstract read
In one paragraph

Article in Epilepsia open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Nandani AdhyapakDepartment of Neurology, Neuroscience and Psychiatry & Behavioral Sciences, Baylor College of Medicine, Houston, Texas, USA.
Grace E CardenasDepartment of Neurology, Neuroscience and Psychiatry & Behavioral Sciences, Baylor College of Medicine, Houston, Texas, USA.
Mark A AbboudDepartment of Neurology, Neuroscience and Psychiatry & Behavioral Sciences, Baylor College of Medicine, Houston, Texas, USA.
Vaishnav KrishnanDepartment of Neurology, Neuroscience and Psychiatry & Behavioral Sciences, Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-2847-0069

Funding

Dissecting the Developmental and Epileptic Components of Encephalopathy in DEER01NS131399 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI Vaishnav Krishnan · 2023 to 2026
$1.7M
UNRAVELLING THE MECHANISMS OF EPILEPSY-DEPRESSION COMORBIDITY IN A GENETIC MOUSE MODEL OF TEMPORAL LOBE EPILEPSYK08NS110924 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI KRISHNAN, VAISHNAV · 2019 to 2023
$960k
Mike Hogg FundNINDS NIH HHS K08 NS110924NINDS NIH HHS K08NS110924NINDS NIH HHS R01 NS131399NINDS NIH HHS R01NS131399
6 · The paper itself

Abstract

objectiveRest-activity rhythms (RARs) are perturbed in many forms of neuropsychiatric illness. In this study, we applied wrist actigraphy to describe RAR perturbations in intellectually disabled adults with epilepsy ("E + ID"), using a cross-sectional case-control design. We examined whether RAR phenotypes correlated with epilepsy severity, deficits in adaptive function, and/or comorbid psychopathology.

methodsCaregivers of E + ID subjects provided informed consent during routine ambulatory clinic visits and were asked to complete standardized surveys of overall epilepsy severity (GASE, Global Assessment of Severity of Epilepsy), adaptive function (ABAS-3, Adaptive Behavior Assessment System-3) and psychopathology (ABCL, Adult Behavior Checklist). Caregivers were also asked to ensure that subjects wore an Actiwatch-2 device continuously for at least ten days. From actograms, we calculated RAR amplitude, acrophase, robustness, intradaily variability (IV), interdaily stability (IS), and estimates of sleep quantity and timing. We compared these RAR metrics against those from (i) a previously published cohort of adults with epilepsy without ID (E-ID), and (ii) a historical control cohort of age- and sex-matched intellectually able subjects from the Study of Latinos (SOL).

results46 E + ID subjects (median age 26, 47% female) provided a median recording duration of 11 days. Surveys reflected low to extremely low levels of adaptive function and low/subclinical levels of psychopathology. Compared with E-ID and SOL cohorts, E + ID subjects displayed significantly lower measures of RAR amplitude, robustness, and IS, with significantly higher IV and total daily sleep. K-means clustering of E + ID subjects recognized a cluster with pronounced hypoactivity, hypersomnia, and elevated rhythm fragmentation (cluster A), an intermediate group with metrics similar to E-ID, and cluster "C" subjects that featured hyper-robust and high amplitude RARs. All three clusters were similar in age, body mass index, antiseizure medication (ASM) polytherapy, ABAS3, and ABCL scores. SIGNIFICANCE: Adults with epilepsy and intellectual disability display a wide spectrum of RAR phenotypes that do not neatly correlate with measures of adaptive function or epilepsy severity. Prospective studies are necessary to determine whether continuous actigraphic monitoring can sensitively capture changes in chronobiological health that may arise with disease progression, ASM side effects, or other acute health deteriorations. PLAIN LANGUAGE SUMMARY: Rest-activity rhythms (RARs) can be measured using continuously worn wrist activity monitors. We show that compared to controls, adults with epilepsy and intellectual disability (E + ID) display RARs that are more fragmented, weaker in amplitude, and unstable across days. Within our E + ID cohort, we observed a wide spectrum of RAR phenotypes that we clustered into three subtypes, which were similar in overall average measures of adaptive functioning and psychiatric symptoms.

Indexed as

EpilepsyIntellectual DisabilityRestActigraphyAdultCase-Control StudiesCross-Sectional StudiesFemaleHumansMaleMiddle AgedPhenotypeSleepYoung Adultactigraphydevelopmental and epileptic encephalopathyintellectual disabilityrest‐activity rhythmssleep

Identifiers

PMID40492460
PMCPMC12362164

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LicenceCC BY-NC-ND
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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.