# Clinical characteristics and associated factors of constipation patients with type 2 diabetes

**Authors:** Yan Fang, Jiahao Chen, Chendong Ni, Yi Dai, Lili Cai, Xiaohua Yang, Ji Hu, Hong-Hong Zhang

PMC · DOI: 10.3389/fendo.2026.1698701 · Frontiers in Endocrinology · 2026-02-16

## TL;DR

This study explores how glucose control metrics like time in range and glucose variability are linked to constipation in type 2 diabetes patients.

## Contribution

The study identifies a novel association between CGM-derived glucose metrics and constipation risk in T2DM patients.

## Key findings

- Patients with constipation had worse clinical indicators, including higher HbA1c, TC, and LDL-C levels.
- Lower time in range (TIR) and higher glucose coefficient of variation (CV) were significantly correlated with constipation.
- CGM-derived metrics may serve as potential markers for predicting constipation risk in T2DM patients.

## Abstract

The aim of this study was to explore the clinical characteristics and associated factors of constipation in patients with type 2 diabetes (T2DM). Here, we focus on the correlation between time in range (TIR) and coefficient of variation (CV) of glucose and constipation in patients with T2DM.

In the exploratory, cross-sectional study, a total of 120 patients diagnosed with T2DM in the department of Endocrinology and Gastroenterology of Liqun hospital from 2023 to 2024 were recruited. Patients with concurrent constipation were included in the constipation group, and those without concurrent constipation were included in the non-constipation group. Fasting blood indicators of patients were detected, including fasting blood glucose (FBG), 2 hours postgrandial blood glucose (2hPBG), glycosylated hemoglobin type A1C (HbA1c), fasting C-peptide (FCP), homeostasismodel assessment-insulin resistance (HOMA-IR), triglyceride (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C). Blood Glucose was monitored by a silicon-based dynamic system for 14 days, and TIR and CV were calculated by a continuous glucose monitoring system (CGM). In addition, the symptoms of constipation, gastroparesis cardinal symptom index (GCSI), patient assessment of upper gastrointestinal symptom severity index (PAGI-SYM) and patient assessment of quality-of-life index (PAGI-QOL) were evaluated by questionnaires. The impact of TIR and CV for constipation risk was evaluated using receiver operating characteristic (ROC) curves.

1. More serious condition in constipation symptoms, GCSI, VSI, PAGI-SYM and PAGI-QOL scores in the constipation group. 2. Compared with the non-constipation group, the constipation group had longer courses, and higher probabilites of complications of autonomic neuropathy, diabetic nephropathy and hyperlipidemia; 3. Compared with the non-constipated group, FCP was significantly decreased, and HbA1c, TC and LDL-C were significantly increased in the constipation group. 4. TIR and CV were significantly correlated with constipation in patients with T2DM.

Lower TIR and higher CV were associated with constipation in T2DM patients. These findings suggest that CGM-derived metrics may be useful markers of constipation risk and warrant investigation in prospective studies to determine whether improving these parameters can prevent constipation development.

## Linked entities

- **Diseases:** type 2 diabetes (MONDO:0005148), constipation (MONDO:0002203), autonomic neuropathy (MONDO:0001300), diabetic nephropathy (MONDO:0005016), hyperlipidemia (MONDO:0021187)

## Full-text entities

- **Genes:** FCP1 (F-cell production 1) [NCBI Gene 2221] {aka FCP, FCPX, HBFQTL3}, SYMPK (symplekin scaffold protein) [NCBI Gene 8189] {aka Pta1, SPK, SYM}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** nausea (MESH:D009325), Impaired glycemic control (MESH:D007174), abdominal discomfort (MESH:D000007), nephropathy (MESH:D007674), fecal incontinence (MESH:D005242), obese (MESH:D009765), depression (MESH:D003866), T2DM (MESH:D003924), impaired gastric contraction (MESH:D013272), retinopathy (MESH:D058437), diarrhea (MESH:D003967), overweight (MESH:D050177), Constipation (MESH:D003248), decreased appetite (MESH:D001068), cardiac vascular disease (MESH:D006331), chest pain (MESH:D002637), heartburn (MESH:D006356), Gastroparesis (MESH:D018589), Diabetic Peripheral Neuropathy (MESH:D010523), perforation of (MESH:D057112), acute and chronic reactive diseases (MESH:D000208), hypoglycemic (MESH:C000721848), dyskinesia of intestinal tract (MESH:D007410), metabolic dysregulation (MESH:D021081), Diabetic Kidney Disease (MESH:D003928), bloating (MESH:C535647), metabolic disease (MESH:D008659), autonomic (MESH:D001342), enteric neuropathy (MESH:D007418), systemic diseases (MESH:D034721), vomiting (MESH:D014839), esophageal peristalsis disorders (MESH:D004941), Cognitive dysfunction (MESH:D003072), colonic dysmotility (MESH:D003108), autonomic neuropathy (MESH:D009422), hyperlipidemia (MESH:D006949), Peripheral Vascular Disease (MESH:D016491), Cardinal Symptom (MESH:D012816), hyperglycemia (MESH:D006943), dysphagia (MESH:D003680), acid reflux (MESH:D005764), diabetic foot (MESH:D017719), Gastrointestinal Symptom (MESH:D012817), complications (MESH:D008107), consciousness disorders (MESH:D003244), painful neuropathy (MESH:C564945), HbA1c (MESH:D006445), Chronic diabetic complications (MESH:D048909), ESRD (MESH:D007676), Diabetic gastrointestinal diseases (MESH:D005767), Diabetes mellitus (MESH:D003920), Diabetic Retinopathy (MESH:D003930), sudden death (MESH:D003645), DR (MESH:D004370), non-alcoholic fatty liver disease (MESH:D065626), Diabetic Autonomic Neuropathy (MESH:D003929), chronic kidney disease (MESH:D051436), Insulin Resistance (MESH:D007333), anxiety (MESH:D001007), abdominal pain (MESH:D015746)
- **Chemicals:** metformin (MESH:D008687), steroid hormones (MESH:D013256), phospholipids (MESH:D010743), lipid (MESH:D008055), Glycolipids (MESH:D006017), Blood Glucose (MESH:D001786), C-peptide (MESH:D002096), Glucose (MESH:D005947), Cholesterol (MESH:D002784), CV (-), TG (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** A1C, A1C

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950557/full.md

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Source: https://tomesphere.com/paper/PMC12950557