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. 2020 Jan 8;10:787. doi: 10.3389/fendo.2019.00787

Table 2.

Summary of serum 3,5-T2 concentrations in humans observed under physiological (a) and pathophysiological (b) conditions.

a) Physiological conditions:
• Serum 3,5-T2 and 3T1AM concentrations as analyzed by specific mAb-based CLIA do not mirror the dynamics of T3 (or T4) after substitution with T4, T3, or T3-sulfate in healthy individuals or hypothyroid patients
• Inter-individual differences in 3,5-T2 and 3T1AM serum concentrations
• Remarkably stable individual 3,5-T2 and 3T1AM serum concentrations
• Discrepancy between 3,5-T2 serum concentrations determined by CLIA and LC-MS/MS
• No clear correlation to TSH, T4, and T3 concentrations
• No evidence from these studies supporting the postulated metabolic pathway in humans: T4 → T3 → 3,5-T2 → 3T1AM
• Serum 3,5-T2 concentrations are correlated to trigonelline, hippurate, and 3-aminoisobutyrate concentration in urine of healthy individuals (“coffee signature”).
b) Elevated serum concentrations of 3,5-T2 in patients:
• Sepsis
• Non-survivors of ICU
• Postoperative atrial fibrillation (POAF)
• Impaired renal function
• Oral T4 supplementation.