# Insulin Inertia Among People With Type 2 Diabetes Mellitus in Qatar: The INERT‐Q Study

**Authors:** Mohammed Bashir, Noora Al Thani, Abeer Khalid, Obada Khalil, Zaina Alamer, Mohammed Khair Hamad, Gowri Karuppasamy, Mohammed Abufaeid, Mutwakil Elbidairi, Dhabia Al‐Mohnnadi, Tarik Elhadd, Mahmoud Zirie

PMC · DOI: 10.1002/edm2.495 · 2024-06-06

## TL;DR

This study finds that many people with type 2 diabetes in Qatar start insulin too late, leading to poor blood sugar control.

## Contribution

The study quantifies insulin inertia in Qatar and shows that early insulin initiation improves long-term diabetes outcomes.

## Key findings

- Only 32.9% of patients achieved HbA1c targets at 6 months and 1 year after starting insulin.
- Higher HbA1c at insulin initiation correlates with lower chances of meeting glycaemic targets.
- Delaying insulin titration beyond 6 months reduces the likelihood of achieving glycaemic targets at 2 years.

## Abstract

Achieving and maintaining adequate glycaemic control is critical to reduce diabetes‐related complications. Therapeutic inertia is one of the leading causes of suboptimal glycaemic control.

To assess the degree of inertia in insulin initiation and intensification in people with Type 2 diabetes mellitus (DM‐2).

We performed a retrospective longitudinal cohort study and followed DM‐2 2 years before and 2 years after the start of insulin. The primary outcome was the proportion of patients who achieved glycaemic targets (HBA1c ≤ 7.5%) at 6th month, 1st year and 2nd year.

We included 374 predominantly male subjects (62%). The mean age was 55.3 ± 11.3 years, the mean duration of DM‐2 was 12.0 ± 7.3 years, 64.4% were obese, 47.6% had a microvascular disease, and 24.3% had a macrovascular disease. The mean HBA1c at −2nd year and −1st year was 9.2 ± 2.1% and 9.3 ± 2.0%, respectively. The mean HbA1C at the time of insulin initiation was 10.4 ± 2.1%. The mean HBA1c at 6th month, 12th month and 2nd year was 8.5 ± 1.8%, 8.4 ± 1.8% and 8.5 ± 1.7%, respectively. The proportion of subjects who achieved HBA1c targets at 6th month, 12th month and 2nd year was 32.9%, 31.0% and 32.9%, respectively. Multivariate logistic regression analysis showed that achieving HBA1c targets at 6th month and 1st year increases the odds of achieving HBA1c targets at 2nd year (OR 4.87 [2.4–9.6] p < 0.001) and (OR 6.2 [3.2–12.0], p < 0.001), respectively.

In people with DM‐2, there was an alarming delay in starting and titrating insulin. The reduction in HBA1c plateaued at 6th month. Earlier initiation and intensification of insulin therapy are critical to achieving glycaemic targets. More studies are needed to examine the causes of therapeutic inertia from physicians', patients' and systems' points of view.

Type 2 diabetes mellitus (DM‐2) is a progressive disease, and many patients require insulin therapy, particularly those with early‐onset disease.Almost one‐third of the people with DM‐2 had evidence of complications at the time of insulin initiation.The higher the HBA1c at the time of insulin initiation, the lower the chances of achieving glycaemic targets.Delaying insulin titration beyond 6 months reduces the chances of achieving glycaemic targets at 2 years.Earlier insulin initiation and adequate titration are critical to achieving glycaemic targets in people with poorly controlled DM‐2.

Type 2 diabetes mellitus (DM‐2) is a progressive disease, and many patients require insulin therapy, particularly those with early‐onset disease.

Almost one‐third of the people with DM‐2 had evidence of complications at the time of insulin initiation.

The higher the HBA1c at the time of insulin initiation, the lower the chances of achieving glycaemic targets.

Delaying insulin titration beyond 6 months reduces the chances of achieving glycaemic targets at 2 years.

Earlier insulin initiation and adequate titration are critical to achieving glycaemic targets in people with poorly controlled DM‐2.

## Linked entities

- **Diseases:** Type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** microvascular disease (MESH:D017566), Type 2 Diabetes Mellitus (MESH:D003924), DM-2 (MESH:D009223), diabetes (MESH:D003920), macrovascular disease (MESH:D004194), obese (MESH:D009765)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11156521/full.md

---
Source: https://tomesphere.com/paper/PMC11156521