The Sri Lankan Twin Registry: 2012 update
Athula Sumathipala1, Sisira Siribaddana, Mathew Hotopf
1Institute for Research & Development, Colombo, Sri Lanka. athula.sumathipala@kcl.ac.uk
Summary
The Sri Lankan Twin Registry (SLTR) supports genetic research in low- and middle-income countries. It has facilitated studies on psychiatric disorders and cardiovascular health, establishing a biobank and genetic lab.
Area of Science:
- Population Health
- Genetics
- Epidemiology
Background:
- The Sri Lankan Twin Registry (SLTR) was established in 1997 as a vital resource for twin and genetic research in a low- and middle-income country (LMIC).
- It includes a large volunteer cohort (14,120 twins, 119 triplets) and a population-based cohort (19,040 twins, 89 triplets).
- The SLTR has supported significant research, including the Colombo Twin and Singleton Study (CoTaSS 1), investigating psychiatric disorders and gene-environment interactions.
Purpose of the Study:
- To present the Sri Lankan Twin Registry (SLTR) as a unique research infrastructure in a LMIC.
- To highlight ongoing research, including the Colombo Twin and Singleton Study 2 (CoTaSS 2), focusing on cardiovascular and metabolic risk markers.
- To showcase the expansion of SLTR's research scope and its role in global collaborations.
Main Methods:
- Utilizes a comprehensive twin registry with both volunteer and population-based cohorts.
- Employs epidemiological and genetic research methodologies to study disease prevalence and heritability.
- Incorporates the establishment of a biobank and a state-of-the-art genetic laboratory for advanced research.
Main Results:
- The SLTR has facilitated studies on the prevalence and heritability of psychiatric disorders.
- Ongoing research (CoTaSS 2) is examining cardiovascular and metabolic risk markers and their interrelationships.
- The registry has successfully established a biobank and a genetic laboratory, enhancing research capabilities.
Conclusions:
- The SLTR is a successful model for building research infrastructure in LMICs through international partnerships.
- It plays a crucial role in advancing genetic and epidemiological research, particularly in mental and physical health.
- The registry's capacity building, public engagement, and focus on ethics and governance are key to its success.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
Mitral Stenosis II: Clinical features and Diagnostic Tests
Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
Genetic Variation
Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
Genes exist in different versions called alleles, which...
Genes exist in different versions called alleles, which...
Trihybrid Crosses
Trihybrid Crosses
Some of Mendel’s crosses examined three pairs of contrasting characteristics. Such a cross is called a trihybrid cross. A trihybrid cross is a combination of three individual monohybrid crosses. For example, plant height (tall vs. short), seed shape (round vs. wrinkled), and seed color (yellow vs. green).
The F1 generation plants of a trihybrid cross are heterozygous for all three traits and produce eight gametes. Upon self-fertilization, these gametes have an equal chance to...
Some of Mendel’s crosses examined three pairs of contrasting characteristics. Such a cross is called a trihybrid cross. A trihybrid cross is a combination of three individual monohybrid crosses. For example, plant height (tall vs. short), seed shape (round vs. wrinkled), and seed color (yellow vs. green).
The F1 generation plants of a trihybrid cross are heterozygous for all three traits and produce eight gametes. Upon self-fertilization, these gametes have an equal chance to...
Sex Linked Disorders
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.


