A multi-center, prospective cohort study of whole blood gene expression in the tuberculosis-diabetes interaction

• Published in: Scientific reports Vol. 13; no. 1; p. 7769
• Main Authors: Queiroz, Artur T. L., Vinhaes, Caian L., Fukutani, Eduardo R., Gupte, Akshay N., Kumar, Nathella Pavan, Fukutani, Kiyoshi F., Arriaga, María B., Sterling, Timothy R., Babu, Subash, Gaikwad, Sanjay, Karyakarte, Rajesh, Mave, Vidya, Paradhkar, Mandar, Viswanathan, Vijay, Gupta, Amita, Andrade, Bruno B., Kornfeld, Hardy
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 12-05-2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/250/254; 631/250/255; 631/250/256; 692/308; 692/4017; 692/53; Adult; Blood; Cohort analysis; Diabetes; Diabetes mellitus; Diabetes Mellitus - genetics; Diabetes Mellitus - metabolism; Gene Expression; Genomic instability; Humanities and Social Sciences; Humans; Immune response; Insulin resistance; Leukocytes (neutrophilic); Microvasculature; multidisciplinary; Prospective Studies; Science; Science (multidisciplinary); Tuberculosis; Tuberculosis - complications; Tuberculosis - genetics; Tuberculosis, Pulmonary - complications; Tuberculosis, Pulmonary - genetics
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-34847-9

Diabetes mellitus (DM) increases tuberculosis (TB) severity. We compared blood gene expression in adults with pulmonary TB, with or without diabetes mellitus (DM) from sites in Brazil and India. RNA sequencing (RNAseq) performed at baseline and during TB treatment. Publicly available baseline RNAseq data from South Africa and Romania reported by the TANDEM Consortium were also analyzed. Across the sites, differentially expressed genes varied for each condition (DM, TB, and TBDM) and no pattern classified any one group across all sites. A concise signature of TB disease was identified but this was expressed equally in TB and TBDM. Pathway enrichment analysis failed to distinguish TB from TBDM, although there was a trend for greater neutrophil and innate immune pathway activation in TBDM participants. Pathways associated with insulin resistance, metabolic dysfunction, diabetic complications, and chromosomal instability were positively correlated with glycohemoglobin. The immune response to pulmonary TB as reflected by whole blood gene expression is substantially similar with or without comorbid DM. Gene expression pathways associated with the microvascular and macrovascular complications of DM are upregulated during TB, supporting a syndemic interaction between these coprevalent diseases.