Purpose

The Family Investigation of Nephropathy and Diabetes (FIND) is a multicenter study designed to identify genetic determinants of diabetic kidney disease. FIND will be conducted in eleven centers and in many ethnic groups throughout the United States. Two different strategies will be used to localize genes predisposing to kidney disease: a family-based genetic linkage study and a case-control study that utilizes admixture linkage disequilibrium. The center based at the Phoenix office of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK-Phoenix) will conduct family-based linkage studies among American Indian populations in the southwestern United States. Participants (index cases) with diabetes and kidney disease will initially be recruited, and their parents and siblings will also be invited to participate. Genetic material from these participants will be used to genotype markers throughout the genome. Linkage analysis will be conducted to identify particular chromosomal regions containing genes that influence susceptibility to diabetic kidney disease. Linkage analyses will also be used to identify genes influencing traits related to diabetic kidney disease, such as serum creatinine, urinary protein excretion, plasma glucose levels, blood pressure and blood lipid levels. Regions that show evidence for linkage will then be examined in more detail, with both genetic linkage and association studies, to attempt to identify the specific genes that influence diabetic kidney disease, or related traits. The identification of genes that influence susceptibility to diabetic kidney disease will lead to a better understanding of how kidney disease develops. In the long run, this may lead to improved treatment and prevention of diabetic kidney disease.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 99 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Criteria

- INCLUSION CRITERIA:

Index Cases:

Individuals with diabetes and diabetic nephropathy who are at least 18 years of age.

Potential index cases must have at least one sibling, or both parents available as
potential study participants.

Potential index cases must also have diabetic nephropathy. An index case must have
nephropathy that is more severe than microalbuminuria. An index case must meet one of the
following criteria:

1. Biopsy proven diabetic nephropathy (by medical record review):

1. Nodular and/or diffuse increases in the mesangial matrix accumulation; and

2. Thickened glomerular basement membranes and/or arteriolar hyalinization; and

3. Absence of mesangial immunoglobulin or paraprotein deposits by
immunoflorecscence microscopy, absence of amyloid deposits by Congo Red
staining or electron microscopy, absence of electron dense deposits within the
glomerular basement membrane or glomerular capillary subendothelial space; and

4. Overt proteinuria, defined as ACR greater than or equal to 300 mg/g, urinary
protein creatinine ratio greater than or equal to 0.5 g/g, urinary albumin
excretion greater than or equal to 300 mg/24 hr, or urinary protein excretion
greater than or equal to 0.5 g/24 hr.

2. ESRD (including transplant) from presumed diabetic nephropathy:

Diabetes present for at least 5 years prior to the initiation of replacement therapy
and retinopathy at any time;

or Diabetes present for at least 5 years prior to the initiation of replacement
therapy and either greater than or equal to 3 gm protein/24 hours, or a urine
protein (mg)/creatinine (mg) greater than or equal to 3.0 or urinary ACR greater
than or equal to 3000 mg/g or urinary albumin excretion greater than or equal to
3000 mg/24 hours (historical data acceptable);

or retinopathy and either greater than or equal to 3 gm protein/24 hours, or a urine
protein (mg)/creatinine (mg) greater than 3.0 or urinary ACR greater than or equal
to 3000 mg/g or urinary albumin excretion greater than 3000 mg/24 hours (historical
data acceptable).

3. Patient with presumed diabetic nephropathy but not ESRD:

Patient has diabetic retinopathy and either greater than or equal to 1 gram
proteinuria/24 hours or a urine protein (mg)/creatinine (mg) greater than or equal to 1.0
or urinary ACR greater than or equal to 1000 mg/g or urinary albumin excretion greater
than or equal to 1000 mg/24 hours (historical data acceptable);

or first detection of either greater than or equal to 3 gram protein/24 hours or a urine
protein (mg)/creatinine (mg) greater than or equal to 3.0 gram or urinary ACR greater
than or equal to 3000 mg/g or urinary albumin excretion greater than or equal to 3000
mg/24 hours at DM duration greater than or equal to 10 years (historical data
acceptable).

Recruitment of Family Members:

Any available parent or sibling who is at least 18 years of age will be recruited as a
potential participant and will use the same criteria as above.

DNA for individuals in informative families will be submitted to the genotyping
laboratory. An informative family is defined as one for which DNA specimens are available
for the following individuals:

1. The index case and both parents, or

2. The index case and at least one other affected sibling who has diabetes and renal
disease, or

3. The index case and at least one unaffected sibling, defined as an individual who has
had diabetes for at least 10 years and who has no renal disease (based on evidence
obtained from the medical record and from the FIND examination.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Volunteers Volunteers for a genetic study of diabetes and nephropathy

Recruiting Locations

NIDDK, Phoenix
Phoenix, Arizona 85014
Contact:
Robert Hanson, M.D.
602-200-5207
rhanson@phx.niddk.nih.gov

More Details

NCT ID
NCT00342927
Status
Recruiting
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Study Contact

Robert L Hanson, M.D.
(602) 200-5207
rhanson@phx.niddk.nih.gov

Detailed Description

The Family Investigation of Nephropathy and Diabetes (FIND) is a multicenter study designed to identify genetic determinants of diabetic kidney disease. FIND is conducted in eleven centers and in many ethnic groups throughout the United States. Two different strategies are used to localize genes predisposing to kidney disease: a family-based genetic linkage/association study and a case-control study that uses admixture linkage disequilibrium. The center based at the Phoenix office of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK-Phoenix) conducts family-based linkage/association studies among American Indian populations in the southwestern United States, and in the indigenous Micronesian populations of the Territory of Guam and the Commonwealth of the Northern Mariana Islands (CNMI). Participants (index cases) with diabetes and kidney disease are recruited, and their parents and siblings are also invited to participate. Members of target populations who are not related to index cases are also included and offered screening for diabetes and kidney disease; this will facilitate association studies. Genetic material from these participants is used to genotype markers throughout the genome. Linkage and association analyses are conducted to identify particular chromosomal regions containing genes that influence susceptibility to diabetic kidney disease. Linkage and association analyses are also used to identify genes influencing traits related to diabetic kidney disease, such as serum creatinine, urinary protein excretion, plasma glucose levels, blood pressure and blood lipid levels. Genome-wide and candidate gene association studies are also conducted. Regions that show evidence for linkage or association are then examined in more detail, with both genetic linkage and association studies, to attempt to identify the specific genes that influence diabetic kidney disease, or related traits. The identification of genes that influence susceptibility to diabetic kidney disease will lead to a better understanding of how kidney disease develops. In the long run, this may lead to improved treatment and prevention of diabetic kidney disease.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.