CClinicalTrials.gg
Enrolling by invitationNCT07033676Updated Jun 24, 2025

Serum miR-455-5p and Cardiac Structure and Function Parameters in Patients With Hypertensive Heart Disease

An observational study in Hypertension and Heart Disease, sponsored by The University of Hong Kong-Shenzhen Hospital. Enrolling by invitation at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-06-24.

Sponsored by The University of Hong Kong-Shenzhen Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2025, 1 year 3 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
46
Ages
18 Years and older
Sex
All
01

Study summary

Hypertensive heart disease (HHD) is the leading cause of mortality and morbidity worldwide. In 2017, the prevalence of HHD worldwide was 217.9 per 100,000 people, an increase of 7.4% over 1990, which has brought huge financial burden and social and economic losses to the world. Therefore, HHD is a major public health challenge worldwide. In our previous studies, we found that miR-455-5p, a microRNA, could functioned as an inducer to promote cardiac hypertrophy. Because cardiac hypertrophy was a common phenomenon in patients with HHD, so it is interesting to clarify whether miR-455-5p could be employed as a marker to indicate the function and/or structure of heart in the development of HHD. Thus, the purpose of this study was to collect blood samples of hypertensive patients, as well as analysis the correlation between serum miR-455-5p level and cardiac function. The research could help doctors better predict the course of hypertensive heart disease and provide more effective treatments for different patients.

Read the detailed description

The purpose of this study was to collect blood samples of hypertensive patients, in order to clarify the correlation between serum miR-455-5p level and cardiac function. Generally, by using q-PCR assay, miR-455-5p level of each participants will be collected. Besides, SBP, DBP, LVPWd, LVIDd, IVSTd was detected by echocardiography and EF, FS, LVMi, RWT level was further calculated by LVIDd, LVPWd and IVSTd. Finally, the correlation of miR-455-5p level of HHD patients and LVPWd, LVIDd, IVSTd, EF, FS, LVMi, RWT, SBP, DBP was analysed.

02

Conditions studied

  • Hypertension
  • Heart Disease

Keywords

  • miR-455-5p
  • hypertensive heart disease
03

In context

Hypertension

6,689 studies on the registry are indexed under Hypertension; 964 are open to participants now.

This study's planned enrollment of 46 is below the median of 210 across 1,358 observational studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

The University of Hong Kong-Shenzhen Hospital is the lead sponsor of 16 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

45 patients with hypertensive heart disease admitted to Hong-Kong University, Shenzhen Hospital from January 1 to March 10 in 2021 were included in our study. Hypertensive heart disease was defined using the International Classification of Diseases, Ninth and Tenth Revision (ICD-10) codes. Diseases coded as I11.0 and I11.9 in ICD-10 were identified as hypertensive heart disease[1-2].

Inclusion criteria

  • 1. age ≥18 years; 2. male or female; 3. systolic blood pressure ≥140mmHg or (and) diastolic blood pressure > 90mmHg; 4. history of hypertension>1year, NYHA grade I-IV

Exclusion criteria

Exclusion Criteria:

  • hypertensive heart diseases patients with other metabolic diseases or congenital diseases were excluded from the study
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
46 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. Measurement of serum miR-455-5p level

    concentration of microRNA-455-5p in 100ml serum was determined by Elisa assay.

    Time frame: the miR-455-5p level is collected at week 0, 6, 12 and 24.

  2. Measurement of LVPWd and LVPWs

    left ventricular posterior wall thickness in diastole state and systole state are measured and recorded by echocardiography and its affiliated software.

    Time frame: the LVPWd and LVPWs are collected at week 0, 6, 12 and 24.

  3. Measurement of LVIDd and LVIDs

    left ventricular internal diameter in diastole state and systole state are measured and recorded by echocardiography and its affiliated software.

    Time frame: the LVIDd and LVIDs are collected at week 0, 6, 12 and 24.

  4. Measurement of IVSTd and IVSTs

    interventricular septum in diastole state and systole state are measured and recorded by echocardiography and its affiliated software.

    Time frame: the IVSTd and IVSTs are collected at week 0, 6, 12 and 24.

  5. Calculation of LVMi

    left ventricular mass index was calculated based on the formula: LVMi=LVM/BSA; For LVM, LVM(g)=0.8\*1.04\*\[(IVSTd+LVPWd+LVIDd)\^3-LVIDd\^3\]+0.6; For BSA, BSA=\[Body height (cm)\*Body weight (kg)/3600\]\^0.5; Diagnosis of LVH: LVMi(Male)\>115g/m2;LVMi(Female)\>95g/m2

    Time frame: the LVMi is calculated at week 0, 6, 12 and 24.

  6. Measurement of LVEF

    left ventricular ejection fraction are measured and recorded by echocardiography and its affiliated software. Generally, LVEF is range from 50% to 70% is regarded as normal. If LVEF less than 50%, the patient is suspected to suffered cardiac systolic dysfunction.

    Time frame: the EF is calculated at week 0, 6, 12 and 24.

  7. Measurement of FS

    Fractional shortening are measured and recorded by echocardiography and its affiliated software. Generally, FS is range from 25% to 45% is regarded as normal. If FS less than 25%, the patient is suspected to suffered cardiac systolic dysfunction.

    Time frame: the FS is calculated at week 0, 6, 12 and 24.

  8. SBP

    systolic blood pressure was measured by sphygmomanometer. For patients whose SBP is higher than 140mmHg, the patients is regarded as hypertension.

    Time frame: the SBP is collected at week 0, 6, 12 and 24.

  9. DBP

    diastolic blood pressure was measured by sphygmomanometer. For patients whose DBP is higher than 90mmHg, the patients is regarded as hypertension.

    Time frame: the DBP is collected at week 0, 6, 12 and 24.

07

Study locations

1 site
  • the University of Hongkong-Shenzhen Hospital
    Shenzhen, Guangdong, China
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07033676
Lead sponsor
The University of Hong Kong-Shenzhen Hospital
Responsible party
Cai Sidong (Assistant research fellow, The University of Hong Kong-Shenzhen Hospital) — Principal investigator
First posted
Jun 24, 2025
Start date
Jan 1, 2021
Primary completion
Jun 30, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Jun 24, 2025

Study contacts

Assistant research fellow
principal investigator · The University of Hong Kong-Shenzhen Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion