Evidence map›Paper›PMID 41297072›Full record

ArticleComputer methods and programs in biomedicine2026

A SAS macro for multilevel Cosinor analysis.

Margaret M Doyle, Terrence E Murphy, Brienne Miner, Melissa P Knauert

Abstract read
In one paragraph

Article in Computer methods and programs in biomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Margaret M DoyleSection of Geriatrics, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA. Electronic address: Margaret.Doyle@yale.edu.
Terrence E MurphyDepartment of Public Health Sciences, Penn State College of Medicine, Hershey, PA, USA.
Brienne MinerSection of Geriatrics, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Melissa P KnauertSection of Pulmonary, Critical Care, and Sleep Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Funding

Yale Study Support Suite (YES3): Dashboard and Web Portal Software Supporting Research Workflow through integrated, customizable REDCap External ModulesP30AG021342 · NIA · YALE UNIVERSITY · PI Albert C Shaw · 2002 to 2026
$37.9M
Penn State Clinical and Translational Science InstituteUL1TR002014 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KRASCHNEWSKI, JENNIFER L. · 2016 to 2025
$33.7M
Yale University Clinical and Translational Science Award ProgramKL2TR000140 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$2.9M
NCATS NIH HHS KL2 TR000140NCATS NIH HHS UL1 TR002014NIA NIH HHS P30 AG021342
6 · The paper itself

Abstract

BACKGROUND AND

objectiveCosinor analysis allows for the fitting of a cosine curve to describe cyclical variation in periodic data. The analysis provides an intuitive set of estimates that includes the MESOR (Midline Estimating Statistic of Rhythm), i.e., the mid-point of the fitted outcome, the amplitude, i.e., one-half the distance between the MESOR and the peak for normally distributed outcomes, and the acrophase, i.e. the time at which the outcome reaches its peak. Traditionally, most published cosinor analyses were generated though a two-stage approach in which a curve was fit to each individual's data and differences in the estimated cosinor parameters were compared in downstream analyses. More recently multilevel cosinor modeling software has been developed which allows for the simultaneous modeling of data from multiple individuals. In addition to simplifying the model building process, the advantage of multilevel vs. two-stage cosinor analysis includes the option to fit more complex models and, likely, an improvement in fit for each individual's data. However, to our knowledge, there are no SAS procedures or macros that assist users with this analytical approach.

methodsIn this paper we introduce multilevel cosinor models and SAS macros we have developed to perform these analyses. In addition, we compare model fit between the multilevel and two-stage methods.

resultsThe SAS macros presented in this paper allow users to select the best random variable specification for the unconditional cosinor model and add a dichotomous grouping variable to detect differences in parameters across groups. At each step of model building, parameter estimates, measures of model fit and graphical output help the user understand the model derived and its appropriateness for their data. Results of cross-validation analyses are presented that illustrate the superior fit of the multilevel over the single-level approach for the dataset utilized in the examples.

conclusionsMultilevel cosinor analysis extends the single subject cosinor model by allowing for more convenient model selection and may provide a better fit for each individual's data. We are hopeful that this manuscript will introduce more researchers to this analytical technique and allow them to apply it in their own research.

Indexed as

SoftwareAlgorithmsHumansModels, StatisticalMultilevel AnalysisAcrophaseCircadianCosinorGrowth modelsMesorMultilevelNadirRSAS

Identifiers

PMID41297072
PMCPMC13238948

What OpenQuestion holds

Textmetadata
LicenceTDM
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.