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Tytuł pozycji:

Correlation between classical transient receptor potential channel 1 gene polymorphism and microalbuminuria in patients with primary hypertension.

Tytuł:
Correlation between classical transient receptor potential channel 1 gene polymorphism and microalbuminuria in patients with primary hypertension.
Autorzy:
Zhang Y; Department of Hypertension, The First Affiliated Hospital of Xinjiang Medical University, Urumqi,Xinjiang, China.
Maitikuerban B; Department of General Practice, Hetian Region People's Hospital, Hetian,Xinjiang, China.
Chen Y; Department of Hypertension, The First Affiliated Hospital of Xinjiang Medical University, Urumqi,Xinjiang, China.
Li Y; Second Department of General Internal Medicine, The First Affiliated Hospital of Xinjiang Medical University, Urumqi,Xinjiang, China.
Cao Y; Department of Hypertension, The First Affiliated Hospital of Xinjiang Medical University, Urumqi,Xinjiang, China.
Xu X; Department of Hypertension, The First Affiliated Hospital of Xinjiang Medical University, Urumqi,Xinjiang, China.
Źródło:
Clinical and experimental hypertension (New York, N.Y. : 1993) [Clin Exp Hypertens] 2021 Jul 04; Vol. 43 (5), pp. 443-449. Date of Electronic Publication: 2021 Apr 20.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Publication: London : Informa Healthcare
Original Publication: New York, N.Y. : Marcel Dekker, Inc., c1993-
MeSH Terms:
Albuminuria/*complications
Albuminuria/*genetics
Essential Hypertension/*complications
Essential Hypertension/*genetics
Polymorphism, Single Nucleotide/*genetics
TRPC Cation Channels/*genetics
Albuminuria/urine ; Essential Hypertension/physiopathology ; Essential Hypertension/urine ; Female ; Gene Frequency/genetics ; Humans ; Logistic Models ; Male ; Middle Aged ; Risk Factors
Contributed Indexing:
Keywords: TRPC1 gene; microalbuminuria; primary hypertension; single nucleotide polymorphism
Substance Nomenclature:
0 (TRPC Cation Channels)
0 (transient receptor potential cation channel, subfamily C, member 1)
Entry Date(s):
Date Created: 20210420 Date Completed: 20210715 Latest Revision: 20220424
Update Code:
20240104
DOI:
10.1080/10641963.2021.1901107
PMID:
33877007
Czasopismo naukowe
Objective: To investigate the correlation between transient receptor potential channel 1 ( TRPC1 ) gene polymorphism and microalbuminuria in patients with primary hypertension. Methods : A total of 468 patients with primary hypertension were admitted to the Department of Hypertension of the First Affiliated Hospital of Xinjiang Medical University from April 2015 to November 2017. According to microalbuminuria, the patients were divided into two groups: high urinary albumin group (EH+mALB group, n = 71) and normal urinary microalbuminuria group (EH group, n = 397). The Sequenom detection technology was used for genotyping the single nucleotide polymorphism (SNP) sites of the TRPC1 gene, such as rs1382688, rs3821647, rs7638459, rs953239, and rs7621642.
Results: (1) No significant differences were detected in gender, smoking history, drinking history, family history, course of hypertension, fasting blood glucose, urea, creatinine, triglyceride, total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, glycosylated hemoglobin, vitamin D, homocysteine, and cystatin C between the two groups ( P > .05). However, age, body mass index (BMI), 24-h mean systolic and diastolic blood pressure, and 24-h average pulse pressure were statistically significant ( P < .05). (2) No significant difference was detected in the distribution frequency of the polymorphisms of the TRPC1 gene between the two groups ( P > .05), while the genotype, allele, and recessive model of rs7638459 differed significantly difference ( P < .05). (3) Logistic regression analysis showed that BMI and rs7638459 CC genotype were the risk factors of increased microalbuminuria in patients with primary hypertension.
Conclusion: TRPC1 gene polymorphism is associated with increased microalbuminuria in patients with primary hypertension. The CC genotype of rs7638459 may increase the risk of microalbuminuria in patients with essential hypertension, while BMI and rs7638459 CC genotype may be the risk factors of increased microalbuminuria in patients with primary hypertension.
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