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CompletedNCT00365235Updated Jan 12, 2012

Understanding the Genetic Basis of Familial Combined Hyperlipidemia in Mexican Individuals

An observational study in Hyperlipidemia, Familial Combined and Coronary Disease, sponsored by University of California, Los Angeles. Completed at 1 site in Mexico. Open to participants aged 10 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-01-12.

Sponsored by University of California, Los Angeles · Observational

Study type
Observational
Model
Family-based
Time perspective
Cross-sectional
Enrollment
998
Ages
10 Years to 80 Years
Sex
All
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Study summary

Familial combined hyperlipidemia (FCHL) is an inherited disorder characterized by elevated levels of cholesterol and triglycerides; it often occurs in Mexican individuals with coronary heart disease (CHD). The purpose of this study is to identify the specific genes that predispose Mexican individuals to FCHL.

Read the detailed description

CHD is the leading cause of death in Mexico. Dyslipidemia that is characterized by high total cholesterol, high triglycerides, and low "good" high-density lipoprotein (HDL) cholesterol is a risk factor for developing CHD. Research has shown that the Mexican population has an increased tendency towards dyslipidemia, but it is not known what genetic factors contribute to this predisposition. This study will examine the genetic basis of FCHL, which is an inherited form of dyslipidemia characterized by elevated levels of total cholesterol and triglycerides. FCHL is a major contributing factor in CHD; 20% of individuals with CHD under the age of 60 have FCHL. The purpose of this study is to identify and characterize the specific DNA sequence variations that predispose Mexican individuals to FCHL. Results of this study may aid in the development of appropriate prevention and screening techniques.

This study will enroll individuals in Mexico who have FCHL. Participants will attend one study visit for blood collection and DNA sampling. Family members of participants will be contacted and asked to provide a DNA sample also. A select group of participants will return for a second study visit for RNA sampling. Study researchers will analyze participants' DNA and RNA samples, as well as two FCHL genes identified in previous research studies.

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Conditions studied

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In context

Coronary Disease

2,839 studies on the registry are indexed under Coronary Disease; 311 are open to participants now.

This study's enrollment of 998 is above the median of 460 across 953 observational studies indexed under Coronary Disease.

Browse Coronary Disease studies →

Lead sponsor

University of California, Los Angeles is the lead sponsor of 1,142 studies on the registry; 192 are open to participants now.

Of its 91 completed or terminated interventional studies of FDA-regulated products, 66 (73%) have results posted.

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

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Who can participate

Ages eligible
10 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Study subjects are Mexicans visiting the Dyslipidemia Clinic at the Instituto Nacional de Ciencias Medicas y Nutricion, Salvador Zubiran, Mexico City, and their family members

Inclusion criteria

  • Elevated levels of serum total cholesterol, triglycerides, or both
  • Elevated levels of serum apolipoprotein B (using the Mexican population percentiles)

Exclusion criteria

Exclusion Criteria:

  • Tendon xanthomas
  • Kidney disease
  • Thyroid disorder
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Study design

Observational model
Family-based
Time perspective
Cross-sectional
Enrollment
998 participants (actual)
Biospecimen retention
Samples with dna
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What researchers measure

Primary outcomes

  1. Identifying the specific genes that predispose Mexican individuals to FCHL

    Time frame: Measured through the use of genetic samples

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Study locations

1 site
  • Instituto Nacional De Ciencias Medicas y Nutricion
    Mexico City, 14000, Mexico
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 12, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00365235
Lead sponsor
University of California, Los Angeles
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Responsible party
Paivi Pajukanta (Professor, University of California, Los Angeles) — Principal investigator
First posted
Aug 17, 2006
Start date
Jul 2006
Primary completion
Jun 2011
Completion
Jun 2011
Last update
Jan 12, 2012

Study contacts

Paivi E. Pajukanta, MD, PhD
principal investigator · David Geffen School of Medicine at UCLA, Department of Human Genetics
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2012. You cannot join it, but the record below documents what was studied.

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