Table 2

IOC REDs CAT2 Severity/Risk Assessment Tool that implements primary, secondary and potential indicators into a traffic-light criterion outlined in figure 2

REDs indicatorReferences
Severe primary indicators (count as two primary indicators)
 Primary amenorrhea (Females: primary amenorrhea is indicated when there has been a failure to menstruate by age 15 in the presence of normal secondary sexual development (two SD above the mean of 13 years), or within 5 years after breast development if that occurs before age 10; or prolonged secondary amenorrhea (absence of 12 or more consecutive menstrual cycles) due to FHA 5 39 51 163 181
 Clinically low free or total testosterone (Males: below the reference range) 53 82 83 182–184
Primary indicators
 Secondary amenorrhea (Females: absence of 3–11 consecutive menstrual cycles) caused by FHA 5 39 51 163
 Subclinically low total or free testosterone (Males: within the lowest 25% (quartile) of the reference range) 53 82 83 182–185
 Subclinically or clinically low total or free T3 (within or below the lowest 25% (quartile) of the reference range) 53 182 186
 History of ≥1 high-risk (femoral neck, sacrum, pelvis) or ≥2 low-risk BSI (all other BSI locations) within the previous 2 years or absence of ≥6 months from training due to BSI in the previous 2 years 39 115
  Pre-menopausal females and males <50 years old: BMD Z-score* <-1 at the lumbar spine, total hip, or femoral neck or decrease in BMD Z-score from prior testing
  Children/adolescents: BMD Z-score* <−1 at the lumbar spine or TBLH or decrease in BMD Z-score from prior testing (can occur from bone loss or inadequate bone accrual).
116 117 119 120
 A negative deviation of a paediatric or adolescent athlete’s previous growth trajectory (height and/or weight) 174 175
 An elevated score for the EDE-Q global (>2.30 in females; >1.68 in males) and/or clinically diagnosed DSM-5-TR-defined Eating Disorder (only 1 primary indicator for either or both outcomes) 122 124 130 133 134 187
Secondary Indicators
 Oligomenorrhea caused by FHA (>35 days between periods for a maximum of 8 periods/year) 5 39 51 163
 History of 1 low-risk BSI (see high vs low-risk definition above) within the previous 2 years and absence of <6 months from training due to BSI in the previous 2 years 39 115
 Elevated total or LDL cholesterol (above reference range) 81 135 139
 Clinically diagnosed depression and/or anxiety (only 1 secondary indicator for either or both outcomes) 33 124 188
Potential Indicators (not scored, emerging)†
 Subclinically or clinically low IGF-1 (within or below the lowest 25% (quartile) of the reference range) 182 189 190
 Clinically low blood glucose (below the reference range) 130 189
 Clinically low blood insulin (below the reference range) 23 24 182
 Chronically poor or sudden decline in iron studies (eg, ferritin, iron, transferrin) and/or haemoglobin 17 191–193
 Lack of ovulation (via urinary ovulation detection) 26 51 65 162
 Elevated resting AM or 24-hour urine cortisol (above the reference range or significant change for an individual) 23 24 182 194
 Urinary incontinence (Females) 195–197
 GI or liver dysfunction/adverse GI symptoms at rest and during exercise 27 34 198
 Reduced or low RMR <30 kcal/kg FFM/d or RMR ratio <0.90 153 158 186 199
 Reduced or low libido/sex drive (especially in males) and decreased morning erections 28–30 36
 Symptomatic orthostatic hypotension 171 174 200
 Bradycardia (HR <40 in adult athletes; HR <50 in adolescent athletes) 171 174 175
 Low systolic or diastolic BP (<90/60 mm Hg) 172 176
 Sleep disturbances 75 201 202
 Psychological symptoms (eg, increased stress, anxiety, mood changes, body dissatisfaction and/or body dysmorphia) 27 32 33 122 124 188
 Exercise dependence/addiction 122 130 203 204
 Low BMI 39 174 175
  • Every indicator below requires consideration of a non-LEA-mediated differential diagnosis. All indicators apply to females and males unless indicated. Menstrual cycle status and endogenous sex hormone levels cannot be accurately assessed in athletes who are taking sex hormone-altering medications (eg, hormone-based contraceptives), and thyroid hormone status indicators cannot be accurately assessed in athletes who are taking thyroid medications. All laboratory values should be interpreted in the context of age-and sex-appropriate and laboratory-specific reference ranges. Most REDs data and associated thresholds have been established in pre-menopausal/andropausal adults unless indicated. Disclaimer: This tool should not be used in isolation nor solely for diagnosis, as every indicator requires clinical consideration of a non-LEA-mediated differential diagnosis. Furthermore, the tool is less reliable in situations where it is impossible to assess all indicators (eg, menstrual cycle status in females who are using hormonal contraception). This tool is not a substitute for professional clinical diagnosis, advice and/or treatment from a physician-led team of REDs health and performance experts.

  • *BMD assessed via DXA within ≤6 months. In some situations, using a Z-score from another skeletal site may be warranted [eg, distal 1/3 radius when other sites cannot be measured or including proximal femoral measurements in some older (>15 years) adolescents for whom longitudinal BMD monitoring into adulthood is indicated].119 121 A true BMD decrease (from prior testing) is ideally assessed in comparison to the individual facilities DXA’s Least Significant Change (LSC) based on the facilities calculated coefficient of variation (%CV). As established by ISCD, at the very least, LSC should be 5.3%, 5.0% and 6.9% for the lumbar spine, hip and femoral neck to detect a clinical change.120 121

  • †Potential indicators are purposefully vague in quantification, pending further research to quantify parameters and cut-offs more accurately.

  • Adolescent, <18 years of age; BMD, bone mineral density; BMI, Body Mass Index; BP, blood pressure; BSI, bone stress injuries; DSM-5-TR, Diagnostic and Statistical Manual of Mental Disorders, 5th edition, text revision; DXA, dual-energy X-ray absorptiometry; EDE-Q, Eating Disorder Examination Questionnaire; FFM, fat-free mass; FHA, functional hypothalamic amenorrhea; GI, gastrointestinal; HR, heart rate; IGF-1, insulin-like growth factor 1; kcal, kilocalories; LDL, low-density lipoprotein; RMR, resting metabolic rate; T3, triiodothyronine; T, testosterone; TBLH, total body less head.