PMID- 34113796 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220423 IS - 2574-0954 (Electronic) IS - 2574-0954 (Linking) VI - 10 IP - 2 DP - 2021 Jun TI - Analogous telomeres shortening and different metabolic profile: hypertension versus hypertension/type 2 diabetes mellitus comorbidity. PG - 106-112 LID - 10.1097/XCE.0000000000000232 [doi] AB - BACKGROUND: Eukaryotes chromosomal ends are capped and protected by telomeres, which are noncoding DNA repeats synthesized by telomerase enzyme. The telomerase enzyme is a nucleoprotein encoded by TERC and TERT genes. Naturally, the length of the telomeres shortens with each cell cycle but the shortening is fastened in certain age-related diseases like hypertension (HTN) and type 2 diabetes mellitus (T2DM). MATERIALS AND METHODS: Blood samples (n = 171) were obtained from Kuwaiti subjects with HTN, and HTN/T2DM comorbidity (HTN-DM) and healthy subjects. The leukocyte telomere length (LTL) was measured by SYBR green quantitative rtPCR, and plasma telomerase enzyme was measured by ELISA, in addition, three single nucleotide polymorphisms (SNPs) in telomere-related genes; TERC rs12696304GC, TERT rs2736100CA, and ACYP2 rs6713088GC were genotyped by real-time PCR. RESULTS: Marked LTL shortening in subjects with HTN and HTN-DM compared to healthy subjects, P = 0.043 and P < 0.001, respectively, was noticed. On the contrary, the plasma telomerase enzyme levels and minor allele frequencies and genotypes of the tested SNPs were comparable between the study groups, except for TERT (CA) genotype which was over-represented in HTN (P = 0.037). Furthermore, the comparisons between HTN and HTN-DM revealed significantly higher total cholesterol (P = 0.015) and LDL-C (P = 0.008) in HTN, while higher insulin levels (P < 001), HOMA-IR (P < 001), and BMI (P = 0.004) were observed in HTN-DM. CONCLUSION: This study showed comparable LTL shortening in HTN and HTN-DM, irrespective of plasma telomerase enzyme levels or tested TERC, TERT, and ACYP2 gene polymorphisms, although HTN and HTN-DM differed in several metabolic markers. More studies are required to affirm these observations. CI - Copyright (c) 2020 Wolters Kluwer Health, Inc. All rights reserved. FAU - AlDehaini, Dhuha M B AU - AlDehaini DMB AD - Department of Biochemistry, College of Medicine and Medical Sciences, Arabian Gulf University. AD - Clinical Chemistry Laboratory, Salmaniya Medical Complex Hospital, Manama, Kingdom of Bahrain. FAU - Al-Bustan, Suzanne A AU - Al-Bustan SA AD - Department of Molecular Biology, Kuwait University, Kuwait City, Kuwait. FAU - Malalla, Zainab Hasan Abdulla AU - Malalla ZHA AD - Department of Biochemistry, College of Medicine and Medical Sciences, Arabian Gulf University. FAU - Ali, Muhalab E AU - Ali ME AD - Department of Biochemistry, College of Medicine and Medical Sciences, Arabian Gulf University. FAU - Sater, Mai AU - Sater M AD - Department of Biochemistry, College of Medicine and Medical Sciences, Arabian Gulf University. FAU - Giha, Hayder A AU - Giha HA AD - Department of Biochemistry, College of Medicine and Medical Sciences, Arabian Gulf University. LA - eng PT - Journal Article DEP - 20200903 PL - United States TA - Cardiovasc Endocrinol Metab JT - Cardiovascular endocrinology & metabolism JID - 101730894 PMC - PMC8186511 OTO - NOTNLM OT - Kuwait OT - biochemical profile OT - hypertension OT - single nucleotide polymorphism OT - telomerase OT - telomeres OT - type 2 diabetes mellitus COIS- There are no conflicts of interest. EDAT- 2021/06/12 06:00 MHDA- 2021/06/12 06:01 PMCR- 2020/09/03 CRDT- 2021/06/11 06:50 PHST- 2020/05/04 00:00 [received] PHST- 2020/07/27 00:00 [accepted] PHST- 2021/06/11 06:50 [entrez] PHST- 2021/06/12 06:00 [pubmed] PHST- 2021/06/12 06:01 [medline] PHST- 2020/09/03 00:00 [pmc-release] AID - 10.1097/XCE.0000000000000232 [doi] PST - epublish SO - Cardiovasc Endocrinol Metab. 2020 Sep 3;10(2):106-112. doi: 10.1097/XCE.0000000000000232. eCollection 2021 Jun.