Metformin as Adjunct Therapy in Depression-obesity Comorbidity: Clinical and Genetic Evaluation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorRiphah International University

About this trial

The patients with depression and obesity will receive add-on metformin with antidepressant therapy, which may result in greater improvement in depressive symptoms and BMI reduction compared to antidepressant monotherapy. NEGR1/RPL31P12 gene polymorphisms may influence the comparative efficacy of antidepressant monotherapy versus combination therapy (antidepressant + metformin) in Pakistani patients. Patients with certain variants may respond better or worse to antidepressants and may have different weight outcomes.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age ≥ 18 years

Both males and females

Recurrent depressive disorder (6A71) according to ICD-11,

Asian cut off: Obese and overweight (BMI < 23)

Disqualifiers

Age less than 18

Dementia/ Mentally impaired who can not fill self report performas for inclusion criteria

Patients with comorbid conditions (HTN, CKD) if taking any drug for that condition.

The patient is not an employee of the investigator study site, or a family member of the employees or the investigator, or otherwise dependent on the sponsor, the investigator, or the investigator study site.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Metformin

    Drug

    Tab 500-2000 mg/day (500 mg BD to 1000 mg BD)

  • Antidepressant Therapy

    Drug

    Sertraline 50 mg/day or Duloxetine 60 mg/day or Bupropion XL 150-300 mg/day

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Antidepressant MonotherapyActive comparator 1 intervention
Group B: Adjunctive Metformin TherapyExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Change in Severity of the depression

The change in the total PHQ-9 score between baseline and 4-weeks follow-up is the primary outcome measure. This measure is a patient-rated inventory of depressive symptoms. All items are scored on scales ranging from 0-3 and the sum of the scores provides the total score for the measure. On this scale, higher scores indicate poorer outcomes. Scores 9-19 and 20-27 are considered moderate and severe depression respectively.

Time frame
1 month
2

Change in BMI

Change in Body Mass Index (BMI): BMI will be measured at baseline and study completion and calculated as weight in kilograms divided by height in meters squared (kg/m²). The outcome will be assessed as the change in BMI from baseline. Asian BMI Classification: Underweight: \< 18.5 kg/m² Normal weight: 18.5-22.9 kg/m² Overweight: 23.0-24.9 kg/m² Obesity Class I: 25.0-29.9 kg/m² Obesity Class II: ≥ 30.0 kg/m² BMI reduction \< 1 kg/m²: Minimal change BMI reduction ≥ 1 kg/m²: Clinically meaningful improvement Weight loss ≥ 5% of baseline body weight: Clinically significant weight reduction associated with metabolic health benefits. A decrease in BMI from baseline and/or movement to a lower BMI category will be considered indicative of improvement in obesity-related outcomes.

Time frame
3 months

Secondary outcomes

1

Change in Blood Pressure

Change in Blood Pressure: Blood pressure will be measured in mmHg at baseline, 14 days, 28 days, one month and 3 months.. The outcome will be assessed as the change in systolic and diastolic blood pressure from baseline. Normal blood pressure is \<120/80 mmHg, elevated blood pressure is 120-129/\<80 mmHg, and high blood pressure is ≥130/80 mmHg. A reduction in blood pressure values from baseline will indicate improvement in cardiovascular health status.

Time frame
3 months
2

Change in Blood Sugar Levels

Change in Blood Sugar: Blood glucose levels will be measured at baseline, 14 days, 28 days, one month and 3 months. The outcome will be assessed as the change in blood glucose from baseline. Normal fasting blood glucose is 70-99 mg/dL, prediabetes is 100-125 mg/dL, and diabetes is ≥126 mg/dL. A reduction in blood glucose levels toward the normal range will indicate improvement in glycemic control, whereas increase will be monitored for safety

Time frame
3 months
3

Change in Renal Function tests

Change in Renal Function Tests: Renal function will be monitored by measuring serum creatinine and blood urea levels at baseline and study completion. The outcome will be assessed as the change in these parameters from baseline. Normal serum creatinine is approximately 0.6-1.2 mg/dL, while values \>1.2 mg/dL may indicate impaired renal function. Normal blood urea is approximately 15-40 mg/dL, while values \>40 mg/dL may suggest reduced kidney function or impaired renal clearance. An increase in serum creatinine or blood urea from baseline will be considered indicative of deterioration in renal function, whereas stable values within the normal range will indicate preserved renal function.

Time frame
3 months
4

Change in Liver Function tests

Change in Liver Function Tests (LFTs): Liver function will be monitored at baseline and study completion. The outcome will be assessed as the change in liver enzyme levels and bilirubin from baseline. Alanine Aminotransferase (ALT): Normal 7-56 U/L; elevated \>56 U/L may indicate liver injury. Aspartate Aminotransferase (AST): Normal 10-40 U/L; elevated \>40 U/L may indicate hepatic or muscle injury. Alkaline Phosphatase (ALP): Normal 44-147 U/L; elevated \>147 U/L may suggest cholestatic liver disease or biliary obstruction. Total Bilirubin: Normal 0.2-1.2 mg/dL; elevated \>1.2 mg/dL may indicate impaired liver function or biliary obstruction. Albumin: Normal 3.5-5.0 g/dL; decreased \<3.5 g/dL may indicate impaired hepatic synthetic function.

Time frame
3 months

Other outcomes

1

NEGR1 Polymorphism

To identify genetic polymorphism in NEGR1 in the Pakistani population, genetic polymorphism in NEGR1 in the Pakistani population will be assessed by ARMS PCR assay.

Time frame
1 month
2

RPL31P12

To identify genetic polymorphism in RPL31P12 in the Pakistani population, genetic polymorphism in RPL31P12 in the Pakistani population will be assessed by ARMS PCR assay.

Time frame
1 month

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