Research Article
The Association between Vitamin D Hypovitaminosis and
Cardiovascular Disease Risk in Saudi Diabetic Patients Type II
Abeer Ahmed Alrefai ,
1,2
Elsayed Elsalamony,
3
Sameer H. Fatani,
2
Zeinab A. Kasemy ,
4
Abdulaziz Fatani,
5
and Hala Fawzy Mohamed Kamel
2,6
1
Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Menoufia University,
Shebin El-kom 32511, Egypt
2
Department of Biochemistry, Faculty of Medicine, Umm Al-Qura University, Makkah 21955, Saudi Arabia
3
Internal Medicine Department, Endocrinology Unit, Mansoura University, Mansoura, Egypt
4
Department of Public Health and Community Medicine, Faculty of Medicine, Menoufia University,
Shebine Elkoum 32511, Egypt
5
Faculty of Medicine, King Abdulaziz University, Geda, Saudi Arabia
6
Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Ain Shams University, Cairo 11566, Egypt
Correspondence should be addressed to Abeer Ahmed Alrefai; drabeer1975@hotmail.com
Received 25 May 2022; Revised 14 August 2022; Accepted 5 September 2022; Published 23 September 2022
Academic Editor: Aziz Ur Rehman Aziz
Copyright © 2022 Abeer Ahmed Alrefai et al. is is an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is
properly cited.
We evaluated the prevalence and association of Vitamin D deficiency with glycemic control and CVD risk in T2DM patients.
Serum 25 (OH)D
3
, lipid profile, glucose panel, HbA1c, serum insulin, and HOMA-IR were assessed in 93 T2DM patients and 69
controls. 10 years and lifetime ASCVD risk scores were calculated. e levels of 25(OH)D
3
were significantly low in T2DM
patients compared to the control. T2DM patients with hypovitaminosis D displayed significantly increased FBG, insulin, and
HOMA-IR compared to normovitaminosis. eir lifetime and 10-year ASCVD risk scores were significantly higher regardless of
vitamin D deficiency levels (P 0.006; P 0.023) in comparison to patients with sufficient levels of vitamin D. Among patients,
the lifetime and 10 years of ASCVD risk showed a significant negative correlation with serum 25(OH)D
3
and HDLc (P 0.037;
0.018) (P 0.0001), respectively, and significant positive correlation with T2DM duration, serum insulin, and HOMA-IR
(P 0.018; 0.0001) (P 0.002; 0.001) (P 0.005; 0.001), respectively. e 10-year ASCVD risk exhibited a significant positive
correlation with FBG (P 0.003) and HbA1c (P 0.009). T2DM duration was a predictor of vitamin D deficiency among T2DM
patients (β 0.22; CI 0.002–0.04). ere is a considerable association between lifetime and 10 years of ASCVD risk with
hypovitaminosis D in T2DM, regardless of the deficiency levels which could be predicted by the diabetes duration.
1. Introduction
e deficiency of vitamin D has been identified lately as a
major health concern [1]. As a multifunctional fat-soluble
vitamin, consequences of deficiency of vitamin D might
not only affect musculoskeletal metabolism and func-
tions, but it will modulate many other cellular events,
such as immunological response, cell proliferation and
differentiation, insulin homeostasis, and metabolic
functions as well [2]. us, it might play a vital role in the
pathogenesis of insulin resistance, type 2 diabetes mel-
litus (T2DM), and cardiometabolic complications of
T2DM patients [3]. By the effect of UV light, 7-dehy-
drocholesterol (provitamin D
3
) is converted into (cho-
lecalciferol) vitamin D
3
that is transported to the liver
with dietary vitamin D
2
to be hydroxylated by the enzyme
P 450 vitamin D-25-hydroxylase into 25-hydroxyvitamin
D. Furthermore, hydroxylation occurs in the kidney and
to less extent in monocytes, placenta, and macrophages,
by the enzyme (CYP27B1)25(OH)D31α-hydroxylase
Hindawi
Biochemistry Research International
Volume 2022, Article ID 6097864, 8 pages
https://doi.org/10.1155/2022/6097864