Research Feeds

View All
Characterizing the gut microbiota in females with infertility and preliminary results of a water-soluble dietary fiber intervention study A prebiotic dietary pilot intervention restores faecal metabolites and may be neuroprotective in Parkinson’s Disease Diagnosis of the menopause: NICE guidance and quality standards Causes of Death in End-Stage Kidney Disease: Comparison Between the United States Renal Data System and a Large Integrated Health Care System Factors affecting the absorption and excretion of lead in the rat Factors associated with age at menarche, menstrual knowledge, and hygiene practices among schoolgirls in Sharjah, UAE Cadmium transport in blood serum The non-pathogenic Escherichia coli strain Nissle 1917 – features of a versatile probiotic Structured Exercise Benefits in Euthyroid Graves’ Disease: Improved Capacity, Fatigue, and Relapse Gut Microbiota Regulate Motor Deficits and Neuroinflammation in a Model of Parkinson’s Disease A Pilot Microbiota Study in Parkinson’s Disease Patients versus Control Subjects, and Effects of FTY720 and FTY720-Mitoxy Therapies in Parkinsonian and Multiple System Atrophy Mouse Models Dysbiosis of the Saliva Microbiome in Patients With Polycystic Ovary Syndrome Integrated Microbiome and Host Transcriptome Profiles Link Parkinson’s Disease to Blautia Genus: Evidence From Feces, Blood, and Brain Gut microbiota modulation: a narrative review on a novel strategy for prevention and alleviation of ovarian aging Long-term postmenopausal hormone therapy and endometrial cancer

Risk of rapid progression to dialysis in patients with type 2 diabetes mellitus with and without diabetes-related complications at diagnosis Original paper

Researched by:

  • Dr. Umar ID
    Dr. Umar

    User avatarClinical Pharmacist and Clinical Pharmacy Master’s candidate focused on antibiotic stewardship, AI-driven pharmacy practice, and research that strengthens safe and effective medication use. Experience spans digital health research with Bloomsbury Health (London), pharmacovigilance in patient support programs, and behavioral approaches to mental health care. Published work includes studies on antibiotic use and awareness, AI applications in medicine, postpartum depression management, and patient safety reporting. Developer of an AI-based clinical decision support system designed to enhance antimicrobial stewardship and optimize therapeutic outcomes.

    Read More

November 30, 2025

Researched by:

  • Dr. Umar ID
    Dr. Umar

    User avatarClinical Pharmacist and Clinical Pharmacy Master’s candidate focused on antibiotic stewardship, AI-driven pharmacy practice, and research that strengthens safe and effective medication use. Experience spans digital health research with Bloomsbury Health (London), pharmacovigilance in patient support programs, and behavioral approaches to mental health care. Published work includes studies on antibiotic use and awareness, AI applications in medicine, postpartum depression management, and patient safety reporting. Developer of an AI-based clinical decision support system designed to enhance antimicrobial stewardship and optimize therapeutic outcomes.

    Read More

Last Updated: 2025-11-30

Microbiome Signatures identifies and validates condition-specific microbiome shifts and interventions to accelerate clinical translation. Our multidisciplinary team supports clinicians, researchers, and innovators in turning microbiome science into actionable medicine.

Dr. Umar

Clinical Pharmacist and Clinical Pharmacy Master’s candidate focused on antibiotic stewardship, AI-driven pharmacy practice, and research that strengthens safe and effective medication use. Experience spans digital health research with Bloomsbury Health (London), pharmacovigilance in patient support programs, and behavioral approaches to mental health care. Published work includes studies on antibiotic use and awareness, AI applications in medicine, postpartum depression management, and patient safety reporting. Developer of an AI-based clinical decision support system designed to enhance antimicrobial stewardship and optimize therapeutic outcomes.

What was studied?

This study examined the rapid progression to dialysis in adults with newly diagnosed type 2 diabetes mellitus, focusing on how diabetes-related complications at diagnosis influence this risk. The analysis used nationwide health insurance data from Taiwan to follow over one million individuals for five years, determining whether early complications dramatically accelerate kidney decline leading to dialysis. Because rapid progression to dialysis is a clinical endpoint shaped strongly by metabolic dysfunction, chronic inflammation, and vascular injury, this research helps clarify how early disease severity signals later renal failure risk. This question also echoes the broader clinical challenge of detecting metabolically driven tissue damage early—an issue aligned with understanding systemic microbiome-linked metabolic stress, though the present study did not directly assess microbiome signatures.

Who was studied?

The population included 1,016,018 adults in Taiwan diagnosed with type 2 diabetes between 2005 and 2013, all aged ≥20 years and free of prior renal failure or transplant. Of these, 25.38% already had at least one diabetes-related complication at diagnosis, including neuropathy, retinopathy, and nephropathy. Individuals were tracked for five years to determine whether dialysis was initiated, using Taiwan’s Registry of Catastrophic Illness. This large cohort provided detailed demographic, socioeconomic, and comorbidity data, allowing the study to explore how disease severity, represented by the Diabetes Complications Severity Index (DCSI), predicts renal outcomes. The dataset’s scale supports strong generalizability for populations with high diabetes prevalence and delayed diagnosis.

Most important findings

The presence and severity of complications at diabetes diagnosis strongly predicted renal decline. Patients with complications had a 9.55-fold higher risk of requiring dialysis within five years compared with those without complications. Higher DCSI scores were associated with stepwise increases in dialysis risk, rising to a 67.56-fold increase among individuals with scores ≥5. Those with three or more complications had a 36.12-fold increased risk, demonstrating that cumulative organ damage sharply accelerates kidney failure. While not directly assessed, these findings intersect with microbiome-related pathophysiology: systemic inflammation, metabolic endotoxemia, and immune dysregulation—often microbiome-linked—are known accelerants of microvascular and renal injury. The study’s dataset reveals clear phenotypic patterns that may later map onto specific microbial signatures associated with nephropathy-prone metabolic states.

Predictor CategoryComparatorIncreased Dialysis RiskInterpretation
Complications at diagnosisNone9.55×Early damage signals aggressive disease trajectory
DCSI score = 1Score 01.97×Mild early injury already increases risk
DCSI score ≥5Score 067.56×Severe multi-system injury predicts rapid decline
≥3 complicationsNone36.12×Multiple organ involvement elevates renal vulnerability

Key implications

Rapid progression to dialysis is far more likely when diabetes is diagnosed after complications have already begun, highlighting missed opportunities for early detection. Clinically, this reinforces the need for aggressive screening, early glycemic control, and perhaps metabolic-inflammation assessments. Although microbiome data were not included, the patterns observed parallel known microbially influenced processes such as endothelial dysfunction and chronic immune activation. A future microbiome-signatures database could integrate phenotypes like high DCSI scores or early nephropathy to identify microbial patterns that precede tissue damage, enabling pre-clinical risk prediction.

Citation

Shih HM, Tsai WC, Wu PY, Chiu LT, Kung PT. Risk of rapid progression to dialysis in patients with type 2 diabetes mellitus with and without diabetes-related complications at diagnosis. Scientific Reports. 2023;13:16366. doi:10.1038/s41598-023-43513-z

Join the Roundtable

Contribute to published consensus reports, connect with top clinicians and researchers, and receive exclusive invitations to roundtable conferences.