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Brief Summary

Healthy volunteers and patients with diseases that involve problems clearing mucus from the lungs will be examined and tested to better understand the reasons for recurring lung infections in these patients and to try to develop better ways to diagnose and treat them. The study will also try to identify the genes responsible for these diseases. Healthy volunteers 18 years of age and older and patients 2 years of age or older with suspected primary ciliary dyskinesia (PCD), variant cystic fibrosis (CF) or pseudohypoaldosteronism (PHA) may be eligible for this study. Patients enrolled in the Natural History Study of Nontuberculous Mycobacteria at NIH or other NIH natural history protocols may also be enrolled. Participants undergo the following tests and procedures during a 1-day visit at the NIH Clinical Center, as follows: All patients and normal volunteers have the following procedures:

Physical examination and review of medical and genetic history and family genetic history.
Lung function test and measurement of oxygen saturation level.
Nitric oxide measurement to measure the amount of nitric oxide production in the nose: A small tube is placed in the nose while the subject breathes through the mouth into a cardboard tube. All patients have the following additional procedures:
Blood tests for liver and kidney function, blood count, immunoglobulins and pregnancy test (where appropriate).
Blood test or buccal scrape (brushing the inside of the cheek) to obtain DNA to look for gene mutations that cause PCD, CF or PHA.
Scrape biopsy of cell lining the inside of the nose: A small toothpick-sized plastic stick with a tiny cup on the end is used to get nasal lining cells to look at the cilia (hair-like structures that move mucus).
Semen analysis (in some men) to test sperm tail function or structure. Patients suspected of having a variant of CF or PHA, including nontuberculous mycobacterial lung disease, have the following additional procedures:
Sweat chloride test: A medicine is placed on the arm to produce sweat; then, a very low level of electric current is applied for 5 to 12 minutes. Sweat is collected in a plastic tube and tested for salt content.
Blood draw for CF genetic testing, if necessary, and to measure levels of the enzyme trypsin.
Saliva collection to measure sodium and chloride content.
Nasal potential difference to measure the electrical activity of the cells lining the inside of the nose: A soft plastic tube filled with a salt solution is passed into the nasal passage and a sterile needle is placed under the skin of the arm. This test provides information about how the lining of the nose is able to get used to changes in temperature and humidity. (Normal volunteers also have this test.)

Conditions

Chronic Granulomatous Disease Cystic Fibrosis Nontuberculous Mycobacterial Infection Primary Ciliary Dyskinesia Pseudohypoaldosteronism

Keywords

Nontuberculous Mycobacterial InfectionPrimary Ciliary DyskinesiaCystic FibrosisPseudohypoaldosteronismChronic Granulomatous DiseaseNatural HistoryMycobacterial InfectionPCDCFPHAHealthy VolunteerHV

Outcome Measures

Primary Outcomes (1)

PCD compatible clinical phenotype or sibling with PCD, plus defect in ciliary ultrastructure
compatible clinical phenotype (sinopulmonary disease and/or neonatal respiratory disorder plus or minus situs inversus) or sibling with PCD, plus defect in ciliary ultrastructure (inner or outer dynein arm; radial spoke; central complex)
6 years

Study Arms (2)

1

Normal

2

patients with Genetic Disorders of Mucociliary Clearance

Eligibility Criteria

Age2 Years - 65 Years

Sexall

Healthy VolunteersNo

Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

There are approximately 100 patients who have been referred to the Clinical Center at NIH, or who have contacted us directly for evaluation of nontuberculous mycobacterial lung disease. Most of these are post-menopausal Caucasian women. Some had known diagnoses of CF or PCD at the time of referral and others have been subsequently diagnosed with these disorders after evaluation here. This population likely reflects a concentrated source population of potential cases of PCD and variant CF to feed into the Consortium. Additionally, the Clinical Center will serve as a referral site for cases of suspected PCD, variant CF, and PHA who don't necessarily have nontuberculous mycobacterial infections. These referrals will likely be concentrated in the National Capital Area and constitute a minority of the patients evaluated on the protocol.

You may qualify if:

Sponsors & Collaborators

National Heart, Lung, and Blood Institute (NHLBI)
NIHlead

Study Sites (1)

National Institutes of Health Clinical Center

Bethesda, Maryland, 20892, United States

MeSH Terms

Conditions

Cystic FibrosisPseudohypoaldosteronismGranulomatous Disease, ChronicCiliary Motility DisordersMycobacterium Infections

Condition Hierarchy (Ancestors)

Pancreatic DiseasesDigestive System DiseasesLung DiseasesRespiratory Tract DiseasesGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesInfant, Newborn, DiseasesRenal Tubular Transport, Inborn ErrorsKidney Diseases

Study Officials

Andrew J Lipton, M.D.
National Heart, Lung, and Blood Institute (NHLBI)
PRINCIPAL INVESTIGATOR

Enrollment

87 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE CONTROL
Time Perspective: CROSS SECTIONAL
Sponsor Type: NIH
Responsible Party: SPONSOR

Study Record Dates

First Submitted

August 23, 2006

First Posted

August 24, 2006

Study Start

October 17, 2006

Actual (reported)

The criteria for participants to enter this study mandates that each patient either be enrolled in the 01-I-0202, Natural History, Genetics, Phenotype, and Treatment of Mycobacterial Infections or related NIH Natural History Protocol, or if referred as part of the Consortium, have received a standard (current clinical practice) diagnostic evaluation that includes testing for asthma, severe gastroesophageal reflux and/or classic CF, prior to enrolling in the Consortium study. Healthy adult control participants will be enrolled for comparison assessment of noninvasive nasal nitric oxide and nasal potential difference measurements only. The health status of these control participants will be assessed with the standardized clinical history, family history, physical exam including height and weight, vital signs, oximetry, and spirometry measurements.
To enter the study, individuals with a suspected mucociliary clearance defect (n=100) must be age 2 years or older and meet one of the 4 following profiles:
Have known or suspected nontuberculous mycobacterial lung disease and enrolled in Protocol 01-I-0202, Natural History, Genetics, Phenotype, and Treatment of Mycobacterial Infections.
Have high suspicion for the diagnosis of PCD, based on ciliary ultrastructural changes on EM (if performed elsewhere prior to referral) or clinical features (chronic sinopulmonary disease, chronic otitis media, history of neonatal respiratory distress or situs inversus), or PCD in a sibling and one of the clinical features of PCD.
Have chronic sino-pulmonary disease with clinical features that overlap with variant CF and PCD, but with diagnostic tests to rule out classical CF (sweat Cl- testing and CF gene mutation screening). This may include patients with other known immune deficiencies such as chronic granulomatous disease followed on NIH natural history protocols.
Known or suspected PHA (or variant PHA), which might include elevated (or borderline) sweat Cl- values.
To enter the study as a healthy control (n=25), individuals must be age 18 or older and free of any known disease, chronic medical conditions, family history of cystic fibrosis or primary ciliary dyskinesia, or any cognitive impairment or significant disability that might preclude voluntary consent or the ability to safely comply with the instructions or sit through the testing.

Genetic Disorders of Mucociliary Clearance in Nontuberculous Mycobacterial Lung Disease

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Study Arms (2)

1

2

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Links

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations

Genetic Disorders of Mucociliary Clearance in Nontuberculous Mycobacterial Lung Disease

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Study Arms (2)

1

2

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Links

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations