Commentary: “TRIB3 promoter 33 bp VNTR is associated with the risk of cerebrovascular disease in type 2 diabetic patients”
Year: 2026
Type: editorial
Abstract: We read with interest the article by Lai et al. (2022) 1 on the association of the 33bp Variable Number of Tandem Repeat (VNTR) in the TRIB3 promoter region with the risk of cerebrovascular disease. While the study presents intriguing findings, we believe several important concerns warrant further discussion.For instance, as the authors state, the VNTR in the TRIB3 promoter could affect TRIB3 transcription. As the authors also note, a previous study by Örd et 1 , even though it is heavily implied in the Supplementary materials. This lack of clarity is more evident when considering the paragraph "Statistical analysis" in the section "Materials and methods". Here, it is reported that the authors "divided patients into three groups based on the total number of TRIB3 33bp tandem repeats in both alleles: low number of 33bp tandem repeats (repeats≤6), intermediate number of 33bp tandem repeats (68)". The sentence's phrasing is ambiguous, leading readers to assume that the number of repeats in the individual's genotype was summed to classify the individual into one of the three groups mentioned, even though it does not state this explicitly.Our most serious concern arises from the classification method used by Lai and colleagues 1 . As a matter of fact, classifying individuals by summing the number of tandem repeats that make up that individual's VNTR genotype is unconventional at best. This type of classification could assign the same functional role to genotypes that may have different effects on phenotype expression, as, for example, would happen with the 2/5 and 3/4 genotypes. While we acknowledge this classification could be appealing for statistical power considerations, this approach assumes a linear dose-response effect, which has not been established for this specific locus, and may overlook non-additive dynamics, such as threshold effects or allele-specific regulatory mechanisms.In addition to the concerns stated above, we compared the frequencies of the VNTR allele reported by Örd et al. 2 with those reported by Lai et al. 1 , using the Han and Southern Han populations from Örd et al. 2 , as the Han population is the major ethnic group in China 3 . Table 1 presents comparisons between Örd et al. 2 and Lai et al. 1 for allele frequencies. As shown, the comparison revealed no significant difference in allele frequency after Fisher's exact test.Furthermore, we checked the Hardy-Weinberg Equilibrium, which showed no discrepancy (P>0.999).The analyses described were deemed necessary to convey important information in genetic association studies 4 , especially when dealing with newly discovered and still poorly characterized VNTRs.While the study by Lai et al. 1 provides valuable preliminary evidence supporting a potential role of the TRIB3 promoter VNTR in cerebrovascular risk among individuals with type 2 diabetes, the variant classification strategy adopted raises important methodological concerns. Providing clearer definitions of alleles, along with a classification system that accounts for both allele-specific and potentially non-additive effects, would enhance the interpretation of results and facilitate comparisons with the existing literature. Given the limited number of studies currently available on this locus, careful standardization of analytical approaches will be essential to advance our understanding of the functional and clinical relevance of the TRIB3-VNTR.
Source: Frontiers in Genetics
Institution: Università di Camerino
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,801
OpenAlex ID: W7137802141