SNP Study of DPP-4 and GLP-1R in Chinese People (Including Diabetes Patients)

• ClinicalTrials.gov Identifier: NCT03108521
• Recruitment Status: Completed
• First Posted: April 11, 2017
• Results First Posted: July 30, 2020
• Last Update Posted: July 30, 2020
• Sponsor: Sichuan Provincial People's Hospital
• Information provided by (Responsible Party): Enwu Long, Sichuan Provincial People's Hospital

Study Description

Brief Summary:

Incretin-based therapy is currently one of the most popular diabetes treatment approaches. However, differences of response ware found in previous studies. We hypothesis that SNPs of DPP-4, GLP-1 and GLP-1R genes may play crucial roles in the response differences. Therefore, this study aims to investigate the correlation of incretin-related gene polymorphism and individual differences in the response of DPP-4 inhibators (take Sitagliptin as an example). In addition, The distribution differences of the SNPs in diabetics and non-diabetics are evaluated to study the relationships between the SNPs and diabetes onsets.

Condition or disease	Intervention/treatment	Phase
Diabetes Mellitus	Drug: Sitagliptin	Phase 4

Detailed Description:

Single Nucleotide Polymorphism (SNP) plays an important role in the differences of clinical manifestations and drug responses of diseases. The vast majority of SNP sites are located in the non-coding region of the gene (about 95%), which is called SNP(non-coding SNP (ncSNP), while the other part of SNP is located in the coding region of the gene, which is called coding SNP (cSNP). Furthermore, cSNP can be divided into two categories: SNP that does not change the encoded amino acid sequence is called synonymous SNP(synonymous SNP, SSNP); SNP that changes amino acid sequence is called SNP(non-synonymous SNP (NSNP). Although not involved in coding amino acid, some ncSNPs may also affect the regulation of protein expression. Therefore, it is of great significance to study the effects of NC SNP and cSNP on the occurrence and development of diseases and drugs.

DPP-4 enzyme inhibitor is combined with DPP-4 enzyme in human body to reduce hydrolysis of active GLP-1, thus increasing the level of endogenous active GLP-1. Active GLP-1 combines with its receptor GLP-1R to promote insulin release and inhibit glucagon release in hyperglycemia state, and produces opposite effect in hypoglycemia state.

Based on the above principles, we speculate that SNP of genes that may affect the hypoglycemic effect of DPP-4 enzyme inhibitor are:

1. SNP of DPP-4 enzyme gene. SNP of DPP-4 enzyme gene may affect the enzyme activity and/or protein expression level of DPP-4. Assuming that the effect of DPP-4 enzyme inhibitor is sufficient, patients with higher DPP-4 enzyme activity are more sensitive to DPP-4 enzyme inhibitor drugs; However, for patients with low DPP-4 enzyme activity, DPP-4 enzyme inhibitor drugs cannot play a stronger role in lowering blood sugar.
2. SNP of GLP-1 gene. SNP of GLP-1 gene may affect activity or expression level of GLP-1. Patients with high GLP-1 level are more sensitive to DPP-4 enzyme inhibitor drugs.
3. SNP of GLP-1R gene. SNP of GLP-1R gene may affect activity or expression level of GLP-1R. Patients with high GLP-1R level are also more susceptible to DPP-4 enzyme inhibitor drugs.

However, studies on the hypoglycemic effect of DPP-4, GLP-1 and their receptors on DPP-4 enzyme inhibitors in the treatment of T2DM are rare, which is not conducive to the evaluation of individualized treatment of such drugs. Therefore, this chapter intends to select SNP sites with high mutation frequencies of DPP-4, GLP-1 and GLP-1R genes to study the mutation frequencies of these SNPs in diabetic patients and non-diabetic patients and their effects on DPP-4 enzyme inhibitor sitagliptin's hypoglycemic effect on T2DM patients.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 119 participants
• Allocation: Non-Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: Study on Polymorphism of DPP-4 and GLP-1R Genes in Chinese Population and Its Empirical Study on Treatment of Diabetes
• Actual Study Start Date: April 21, 2016
• Actual Primary Completion Date: January 4, 2018
• Actual Study Completion Date: October 8, 2018

Arms and Interventions

Arm	Intervention/treatment
Experimental: Sitagliptin group; Patients in this group will accept Sitagliptin phosphate tablets as their intervention. Specifications: Each tablet 100mg (with sitagliptin dollars). Regimen: The recommended dose is 100mg.QD for 3 months.	Drug: Sitagliptin; 100mg.QD for 3 months; Other Name: Januvia
No Intervention: non-T2DM group; Subjects in this group are T2D free. We use their gene information to study SNP differences between T2D patients and non-T2DM people.

Outcome Measures

Primary Outcome Measures :

1. Glycosylated Hemoglobin A1c (HbA1c) [ Time Frame: 12 weeks later ]
   non-T2D subjects only tested HbA1c at baseline. Of the 71 patients who completed the study, 69 collected HbA1c at both baseline and study endpoint, and 2 subjects did not carry out HbA1c measurement for personal reasons.

Secondary Outcome Measures :

1. Types of Gene Polymorphism [ Time Frame: Baseline ]
   24 SNPs genetic points of DPP-4, GLP-1 and GLP-1R.
2. Change in Blood Glucose [ Time Frame: Basline and 12 weeks later. Fasting, 0.5h, 2h,3h after take 75g glucose orally. ]
   Fasting Blood glucose, the postprandial 0.5-hour,2-hour,3-hour blood glucose were measured at baseline and at study end points, and the difference between baseline and study end points were compared.Participants in "Non-T2DM Group" were not taking Sitagliptin, so their blood glucose were not measured.
3. Change in Insulin [ Time Frame: Basline and 12 weeks later. Fasting and 0.5h, 2h,3h after take 75g glucose orally. ]
   Fasting insulin, the postprandial 0.5-hour,2-hour,3-hour insulin were measured at baseline and at study end points, and the difference between baseline and study end points were compared.The changes in fasting insulin, the postprandial 0.5-hour,2-hour,3-hour insulin were compared among patients with different genotypes at baseline and at study end points.Participants in "Non-T2DM Group" were not taking Sitagliptin, so their insulin were not measured.
4. Change in C-peptide [ Time Frame: Basline and 12 weeks later. Fasting and 2h after take 75g glucose orally. ]
   Fasting C-peptide, the postprandial 2-hour C-peptide were measured at baseline and at study end points, and the difference between baseline and study end points were compared.The changes in fasting C-peptide, the postprandial 2-hour C-peptide were compared among patients with different genotypes at baseline and at study end points.Participants in "Non-T2DM Group" were not taking Sitagliptin, so their C-peptide were not measured.

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 70 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

For Sitagliptin group--

Inclusion Criteria:

1. According to diagnostic criteria from Chinese type 2 diabetes prevention and treatment guidelines in diabetes, that published in the Chinese Medical Association Diabetes credits in 2010: Symptoms of diabetes (polydipsia, polyphagia, polyuria, weight loss, itchy skin, blurred vision and other acute metabolic disorders performance caused by hyperglycemia) and RBG≥11.1mmol/L, or fasting plasma glucose (FPG)≥7.0mmol/L, or plasma glucose of 2 hours post glucose-load≥11.1 and patients diagnosed with type 2 diabetes; HbA1c in the range of 7%-10%;
2. Age 40-70 years;
3. Body Mass Index(BMI) 18-40;
4. Did not accepted any antihyperglycemic therapies during the past 4 weeks, or did not change their antihyperglycemic treatment plan in the past 3 months;
5. Did not participate in clinical trials within three months;
6. No serious heart, brain, liver and kidney disease;
7. Signed informed consent.

Exclusion Criteria:

1. Have taken any incretin drugs within recent 1 month;
2. Patients with a weakened immune system;
3. C-peptide < 0.3ng/ml;
4. GLP-1 and DPP4-i drugs allergies;
5. Pregnancy and breast-feeding patients;
6. Patients taking drugs that may affect the metabolism of GLP-1 and DPP4;
7. Patients have serious heart, liver, kidney and respiratory dysfunction; Patients have medullary thyroid carcinoma (MTC) with past history or family history, as well as multiple endocrine neoplasia type 2 syndrome (MEN2);
8. Drug abusing and alcoholism within a year.

For non-T2D group--

No major diseases such as tumors, no dyslipidemia, chronic diseases such as hypertension, and non-diabetic patients whose blood sugar and glycated hemoglobin values cannot meet the criteria for diagnosis of T2DM, and the age is over 50 years old.

Contacts and Locations

Locations

China, Sichuan

Sichuan provincial people's hospital

Chengdu, Sichuan, China, 610000

Sponsors and Collaborators

Sichuan Provincial People's Hospital

Investigators

• Principal Investigator: Enwu Long, Master; Director of Pharmacy department

  Study Documents (Full-Text)

Documents provided by Enwu Long, Sichuan Provincial People's Hospital:

Study Protocol and Statistical Analysis Plan  [PDF] March 1, 2017

More Information

Publications:

Holman N, Young B, Gadsby R. Current prevalence of Type 1 and Type 2 diabetes in adults and children in the UK. Diabet Med. 2015 Sep;32(9):1119-20. doi: 10.1111/dme.12791.

Palermo A, Maggi D, Maurizi AR, Pozzilli P, Buzzetti R. Prevention of type 2 diabetes mellitus: is it feasible? Diabetes Metab Res Rev. 2014 Mar;30 Suppl 1:4-12. doi: 10.1002/dmrr.2513. Review.

Lee YS, Jun HS. Anti-diabetic actions of glucagon-like peptide-1 on pancreatic beta-cells. Metabolism. 2014 Jan;63(1):9-19. doi: 10.1016/j.metabol.2013.09.010. Epub 2013 Oct 17. Review.

• Responsible Party: Enwu Long, Chief Pharmacist, Sichuan Provincial People's Hospital
• ClinicalTrials.gov Identifier: NCT03108521
• Other Study ID Numbers: 2015SZ0182
• First Posted: April 11, 2017
• Results First Posted: July 30, 2020
• Last Update Posted: July 30, 2020
• Last Verified: July 2020

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Enwu Long, Sichuan Provincial People's Hospital:

DPP-4; GLP1R ; gene polymorphism research; diabetes

Additional relevant MeSH terms:

Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Endocrine System Diseases; Sitagliptin Phosphate; Hypoglycemic Agents; Physiological Effects of Drugs; Incretins; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Dipeptidyl-Peptidase IV Inhibitors; Protease Inhibitors; Enzyme Inhibitors; Molecular Mechanisms of Pharmacological Action