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Human herpesvirus 8 infection DNA positivity is associated with low insulin secretion: A case-control study in a sub-Saharan African population with diabetes

  • Eric Lontchi-Yimagou*
  • , Jérôme Legoff
  • , Jean-Louis Nguewa
  • , Philippe Boudou
  • , Eric V Balti
  • , Jean J Noubiap
  • , Vicky Kamwa
  • , Barbara Atogho-Tiedeu
  • , Marcel Azabji-Kenfack
  • , Eric N Djahmeni
  • , Martine Etoa
  • , Gaelle Lemdjo
  • , Vanessa Balla
  • , Mesmin Y Dehayem
  • , Fabienne Foufelle
  • , Jean-Claude Mbanya
  • , Jean-Francois Gautier
  • , Eugene Sobngwi
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Abstract

BACKGROUND: Viruses have been considered potential triggers for the development of diabetes. This study assessed insulin secretion and insulin sensitivity in human herpesvirus 8 (HHV8)-infected and uninfected sub-Saharan African people with diabetes.

METHODS: In all, 173 people with non-autoimmune diabetes were enrolled consecutively: 124 with type 2 diabetes mellitus (T2DM) and 49 with ketosis-prone diabetes (KPD) admitted in hyperglycemic crisis. Those with KPD were further subdivided into those with new-onset ketotic-phase KPD (n = 34) or non-ketotic phase KPD (n = 15). All participants were screened for HHV8-specific antibodies and genomic DNA. Blood samples were collected for analysis of fasting glucose, HbA1c, lipid profile, and C-peptide, with insulin resistance and secretion estimated by homeostasis model assessment.

RESULTS: Among the 173 diabetic participants, 88 (50.9%) were positive for HHV8 antibodies (Ac-HHV8+), including 15 (8.7%) positive for HHV8 DNA (DNA-HHV8+). The seroprevalence of HHV8 was similar between T2DM (55.6%) and KPD (61.2%) subjects. Of those with and without ketotic-phase KPD, 35.3% and 46.7% were Ac-HHV8+, respectively. Body mass index was significantly in lower DNA-HHV8+ than DNA-HHV8- subjects. Low-density lipoprotein and total cholesterol were significantly higher, but C-peptide and homeostatic model assessment of β-cell function (HOMA-β) were significantly lower in DNA-HHV8+ than DNA-HHV8- participants. After excluding DNA-HHV8+ participants, triglyceride concentrations were significantly higher in Ac-HHV8+ (n = 73) than Ac-HHV8- (n = 85) subjects. In contrast, HOMA-β was significantly higher among Ac-HHV8+ than Ac-HHV8- participants.

CONCLUSIONS: In the present study, HHV8 DNA positivity was associated with low insulin secretion in this sub-Saharan African diabetes population.

Original languageEnglish
Pages (from-to)866-873
Number of pages8
JournalJournal of Diabetes
Volume10
Issue number11
DOIs
Publication statusPublished - Nov 2018

Bibliographical note

© 2018 Ruijin Hospital, Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adult
  • Biomarkers/blood
  • Cameroon/epidemiology
  • Case-Control Studies
  • DNA, Viral/genetics
  • Diabetes Mellitus/blood
  • Female
  • Herpesviridae Infections/blood
  • Herpesvirus 8, Human/genetics
  • Host-Pathogen Interactions
  • Humans
  • Insulin/blood
  • Male
  • Middle Aged
  • Risk Factors
  • Secretory Pathway
  • Viral Load

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