Evidence map›Paper›PMID 33982890›Full record

Trial reportArthritis & rheumatology (Hoboken, N.J.)2021

Prediction of Differential Pharmacologic Response in Chronic Pain Using Functional Neuroimaging Biomarkers and a Support Vector Machine Algorithm: An Exploratory Study.

Eric Ichesco, Scott J Peltier, Ishtiaq Mawla, Daniel E Harper, Lynne Pauer, Steven E Harte, Daniel J Clauw, Richard E Harris

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Arthritis & rheumatology (Hoboken, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% of its field
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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Moving towards the use of artificial intelligence in pain management.European journal of pain (London, England) · 2025
    Pooled it
  3. Review
  4. Review
  5. Applications of Artificial Intelligence in Pain Medicine.Current pain and headache reports · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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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

8 authors at 2 institutions in 1 country.

Eric IchescoUniversity of Michigan, Ann Arbor.ORCID 0000-0002-3767-2068
Scott J PeltierUniversity of Michigan, Ann Arbor.
Ishtiaq MawlaUniversity of Michigan, Ann Arbor.ORCID 0000-0003-2030-3976
Daniel E HarperUniversity of Michigan, Ann Arbor.
Lynne PauerPfizer Inc., Groton, Connecticut.
Steven E HarteUniversity of Michigan, Ann Arbor.
Daniel J ClauwUniversity of Michigan, Ann Arbor.
Richard E HarrisUniversity of Michigan, Ann Arbor.
University of Michigan · USPfizer (United States) · US

Funding

Forest Laboratories MD-SAV-09Pfizer A0081211
6 · The paper itself

Abstract

objectiveThere is increasing demand for prediction of chronic pain treatment outcomes using machine-learning models, in order to improve suboptimal pain management. In this exploratory study, we used baseline brain functional connectivity patterns from chronic pain patients with fibromyalgia (FM) to predict whether a patient would respond differentially to either milnacipran or pregabalin, 2 drugs approved by the US Food and Drug Administration for the treatment of FM.

methodsFM patients participated in 2 separate double-blind, placebo-controlled crossover studies, one evaluating milnacipran (n = 15) and one evaluating pregabalin (n = 13). Functional magnetic resonance imaging during rest was performed before treatment to measure intrinsic functional brain connectivity in several brain regions involved in pain processing. A support vector machine algorithm was used to classify FM patients as responders, defined as those with a ≥20% improvement in clinical pain, to either milnacipran or pregabalin.

resultsConnectivity patterns involving the posterior cingulate cortex (PCC) and dorsolateral prefrontal cortex (DLPFC) individually classified pregabalin responders versus milnacipran responders with 77% accuracy. Performance of this classification improved when both PCC and DLPFC connectivity patterns were combined, resulting in a 92% classification accuracy. These results were not related to confounding factors, including head motion, scanner sequence, or hardware status. Connectivity patterns failed to differentiate drug nonresponders across the 2 studies.

conclusionOur findings indicate that brain functional connectivity patterns used in a machine-learning framework differentially predict clinical response to pregabalin and milnacipran in patients with chronic pain. These findings highlight the promise of machine learning in pain prognosis and treatment prediction.

Indexed as

AdultAnalgesicsBiomarkersBrainChronic PainCross-Over StudiesDouble-Blind MethodFemaleFibromyalgiaHumansMagnetic Resonance ImagingMiddle AgedMilnacipranNeuroimagingPregabalinSupport Vector MachineAnalgesicsBiomarkersMilnacipranPregabalin

Identifiers

PMID33982890
PMCPMC8597096
OpenAlexW3162277144

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.