# Progression from Stage 1 to Stage 3 Type 1 Diabetes Characterized by Hypoglycemia

**Authors:** Aakash Nagarapu, Jamie L Felton

PMC · DOI: 10.1210/jcemcr/luaf317 · 2026-03-12

## TL;DR

A 9-year-old boy rapidly progressed from early to advanced type 1 diabetes, marked by hypoglycemia alongside abnormal glucose tolerance.

## Contribution

This case highlights hypoglycemia as a potential biomarker for rapid progression to stage 3 type 1 diabetes.

## Key findings

- A 9-year-old male with multiple islet autoantibodies rapidly progressed from stage 1 to stage 3 T1D.
- The case showed hypoglycemia alongside abnormal glucose tolerance, suggesting hypoglycemia as a possible biomarker.
- This progression occurred despite typical T1D staging criteria indicating normal glucose tolerance in stage 1.

## Abstract

Type 1 diabetes (T1D) development progresses through well-defined stages based on the presence of islet autoantibodies such as insulin autoantibody, glutamic acid decarboxylase autoantibody, tyrosine phosphatase-like protein IA-2 autoantibody, and zinc transporter 8 autoantibody and glycemic status. The presence of multiple islet autoantibodies and normal glucose tolerance is considered stage 1 T1D. Progression to abnormal glucose tolerance, as measured by oral glucose tolerance test or hemoglobin A1c, is considered stage 2, and stage 3 T1D is defined by symptomatic hyperglycemia and the need for insulin replacement therapy. Here, we present a case of a 9-year-old male with rapid progression from stage 1 T1D to stage 3 T1D characterized by persistent, symptomatic hypoglycemia, concurrent with abnormal glucose tolerance. This case demonstrates the paradoxical presence of hypoglycemia and impaired glucose tolerance and suggests that hypoglycemia may be a biomarker of imminent and rapid progression to stage 3 T1D.

## Linked entities

- **Diseases:** type 1 diabetes (MONDO:0005147), hypoglycemia (MONDO:0004946)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SLC30A8 (solute carrier family 30 member 8) [NCBI Gene 169026] {aka ZNT8, ZnT-8}
- **Diseases:** T1D (MESH:D003922), hyperglycemia (MESH:D006943), abnormal glucose tolerance (MESH:D018149), Hypoglycemia (MESH:D007003)
- **Chemicals:** glucose (MESH:D005947)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12981219/full.md

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Source: https://tomesphere.com/paper/PMC12981219