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Development and validation of a priori risk model for extensive white matter lesions in people age 65 years or older: The Dijon MRI study

  • Phillip J Tully
  • , Sarah Qchiqach
  • , Edwige Pereira
  • , Stephanie Debette
  • , Bernard Mazoyer
  • , Christophe Tzourio

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

Abstract

Objectives The objective was to develop and validate a risk model for the likelihood of extensive white matter lesions (extWML) to inform clinicians on whether to proceed with or forgo diagnostic MRI.

Design Population-based cohort study and multivariable prediction model.

Setting Two representative samples from France.

Participants Persons aged 60-80 years without dementia or stroke. Derivation sample n=1714; validation sample n=789.

Primary and secondary outcome measures Volume of extWML (log cm3) was obtained from T2-weighted images in a 1.5 T scanner. 20 candidate risk factors for extWML were evaluated with the C-statistic. Secondary outcomes in validation included incident stroke over 12 years follow-up.

Results The multivariable prediction model included six clinical risk factors (C-statistic=0.61). A cut-off of 7 points on the multivariable prediction model yielded the optimum balance in sensitivity 63.7% and specificity 54.0% and the negative predictive value was high (81.8%), but the positive predictive value was low (31.5%). In further validation, incident stroke risk was associated with continuous scores on the multivariable prediction model (HR 1.02; 95% CI 1.01 to 1.04, P=0.02) and dichotomised scores from the multivariable prediction model (HR 1.28; 95% CI 1.02 to 1.60, P=0.03).

Conclusions A simple clinical risk equation for WML constituted by six variables can inform decisions whether to proceed with or forgo brain MRI. The high-negative predictive value demonstrates potential to reduce unnecessary MRI in the population aged 60-80 years.

Original languageEnglish
Article numbere018328
Pages (from-to)1-9
JournalBMJ Open
Volume7
Issue number12
DOIs
Publication statusPublished - 31 Dec 2017

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