Related Experiment Video
Updated: Apr 9, 2026

Author Spotlight: A Pharmacodissection Approach to Uncover Mechanisms in Cardiovascular Disease Risk Populations
Published on: July 21, 2023
Association of Haptoglobin Polymorphism With Microvascular Complications in Type 2 Diabetes Mellitus: A Case-Control
Prabakaran Vaithinathan1, Alex Roy X1, Sakthivel Vaithiyanathan1
1General Medicine, Vinayaka Mission's Medical College and Hospital, Vinayaka Mission's Research Foundation (Deemed to be University), Karaikal, IND.
Abstract:
Background Type 2 diabetes mellitus (T2DM) is a major public health problem in India, with microvascular complications contributing substantially to morbidity. Haptoglobin (Hp) polymorphisms, particularly the Hp2-2 genotype, have been associated with increased oxidative stress and vascular dysfunction. This case-control study aimed to evaluate the association between Hp polymorphisms and microvascular complications in T2DM patients attending a tertiary care center in South India. Methods A hospital-based case-control study was conducted between July 2023 and December 2024. Eighty-four T2DM patients were enrolled, including 42 cases with documented microvascular complications (nephropathy, retinopathy, and/or neuropathy) and 42 controls without complications. Haptoglobin genotypes (Hp1-1, Hp2-1, Hp2-2) were determined using polymerase chain reaction with sequence-specific primers. Clinical and biochemical parameters, including glycated hemoglobin (HbA1c), lipid profile, and renal function markers, were recorded. Group comparisons were performed using appropriate parametric and non-parametric tests. A p-value <0.05 was considered statistically significant. The study was approved by the Institutional Ethics Committee, and informed consent was obtained from all participants. Results The Hp2-2 genotype was significantly more prevalent among cases compared with controls (62.5-83.3% across complication subgroups vs. 26.2% in controls). Significant associations were observed between Hp2-2 and diabetic nephropathy (p=0.001), neuropathy (p=0.003), and retinopathy (p=0.002). Patients with complications demonstrated higher mean HbA1c levels (8.51 ± 2.20% vs. 7.92 ± 1.29%, p=0.038) and a greater prevalence of microalbuminuria (78.6% vs. 11.9%, p<0.001). Conclusion The Hp2-2 genotype is strongly associated with the presence of microvascular complications in patients with T2DM. These findings suggest that Hp genotyping may have potential utility in identifying individuals at increased risk for diabetic microvascular disease.
More Related Videos
04:36Author Spotlight: Understanding Retinal Vessel Resilience and Disease Progression
Published on: January 12, 2024
08:22Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion
Published on: March 20, 2017
Related Concept Videos
Diabetes Mellitus: Type 2 and Gestational
Diabetes: Symptoms, Diagnosis, and Complications
Diabetes Mellitus: Overview and Type I Subtype
Type 1 diabetes is an autoimmune disease in which the immune system mistakenly attacks and destroys the insulin-producing beta cells in the pancreas. As a result, the body is unable to produce sufficient insulin, and individuals with...
Pathophysiology of Diabetes
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
Carbohydrate Metabolism
Starch accounts for approximately 60% of the carbohydrates consumed by humans. Since amylase enzymes cannot function in the stomach's acidic environment, starch can only be digested in the mouth and small intestine. Simple sugars are found naturally in milk and fruits in...
Multiple Allele Traits