MINI Index (Mucosal Inflammation Noninvasive index)
Aim: to estimate the degree of mucosal inflammation in Crohn’s disease non-invasively
Both the original PCDAI and its mathematically weighted version (wPCDAI) have insufficient correlation with endoscopic activity (r = 0.33–0.45)1,2 To address this gap, the Mucosal Inflammation Non-Invasive Index (MINI) was developed for pediatric Crohn's disease as part of the prospective international ImageKids study 3. It has since been validated across multiple independent cohorts and incorporated into clinical trials evaluating treatment response to exclusive enteral nutrition (EEN), whole-food dietary regimens (e.g., CDED, TASTI-E), anti-TNF agents, and vedolizumab 4-18.
The MINI index incorporates stool frequency and character (derived from the PCDAI stool item), fecal calprotectin, ESR, and CRP in a weighted categorized index to identify children with endoscopic healing. A MINI score of <8 identifies endoscopic healing with 88% sensitivity and 85% specificity (AUC 0.92; 95% CI: 0.89–0.96), significantly outperforming fecal calprotectin alone 3. The likelihood of moderate-to-severe inflammation in patients with a MINI score of <8 is less than 5% 3.
The superiority of the MINI index over calprotectin alone has been confirmed in multiple independent pediatric studies:
EEN & Relapse Prediction: Herman et al. demonstrated high responsiveness of the MINI following EEN therapy, showing it predicted relapse with an area under the receiver operating characteristic curve (AUROC) of 0.90 (95% CI: 0.74–1.0), compared to 0.76 (95% CI: 0.57–0.95) for calprotectin alone 4.
Isolated Small Bowel Disease: In an Italian cohort, the MINI proved to be the most accurate non-invasive tool for isolated ileal disease—superior to both fecal calprotectin alone and wPCDAI—demonstrating a strong correlation with the Simple Endoscopic Score for Crohn's Disease (SES-CD; r = 0.73) 5.
Endoscopic Healing Cutoffs: A validation study from Barcelona demonstrated excellent prediction of endoscopic healing with an AUC of 0.985 (p < .001) using a MINI cutoff of <6 6.
Biologic Response: In the prospective VEDOKIDS trial, the MINI was the strongest predictor of response to vedolizumab in children with Crohn's disease (AUC 0.79 [95% CI: 0.64-0.94]) 8. In addition, multi-center studies evaluating anti-TNF therapy demonstrated that 62% of children achieved mucosal healing (MINI $<8$) at 12 weeks, with MINI-defined response mirroring distinct shifts in the gut microbiome and metabolome 12.
Proactive Monitoring & Dietary Trials: Long-term pediatric studies have utilized the MINI index during proactive drug monitoring and prospective dietary trials (CDED, EEN, and whole-food regimens) to confirm sustained mucosal response and treatment durability non-invasively 9,13,15,17.
Extrapolation & Position Statements: Given its robust non-invasive performance, the MINI index features prominently in international consensus recommendations (ESPGHAN-NASPGHAN) and review frameworks aimed at streamlining pediatric IBD drug approval and long-term monitoring 9,18.
- The MINI index can be scored with either CRP or ESR, but use of both is preferred.
- The ESR/CPR score should be based on the highest of either ESR or CPR.
- The stool item scores the stool pattern during the preceding week.
Patients should initially be categorized as having blood in the stool or not.
- If there is no blood in the stool, scoring should be:
0 - formed stools or up to 1 loose stool daily
4 - 2-5 liquid or very loose stools on 1 or more days
8 - 6 or more liquid or very loose stools on one or more days or any nocturnal diarrhea - If there is blood in the stool, scoring should be:
4 - small amounts of blood (on toilet paper or small spots in stool)
8 - any gross bleeding (large amounts on stools or colors the water in the toilet)
- If there is no blood in the stool, scoring should be: