Study of Resting and Exercising Body Functioning in Freeman-Sheldon Syndrome and Related Conditions

Craniofacial Abnormalities Clinical Trial

— FSS-EDICT I  

Official title:

Freeman-Sheldon Syndrome Evaluation and Diagnosis in Clinical Settings (FSS-EDICT) I: a Case-Control, Cross-Sectional Study of Baseline and Stress Physiology Parameters

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01306994
• Other study ID #: 000079
• Secondary ID: U1111-1120-5931
• Status: Withdrawn
• Start date: March 2014
• Est. completion date: June 2022

Study information

• Verified date: June 2022
• Source: Freeman-Sheldon Research Group, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The hypotheses of the present study of Freeman-Sheldon syndrome (FSS) and related conditions are: (1) that exercise capacity is lower in FSS patients versus normal controls, and the lower exercise capacity is due to changes in the muscles' normal structure and an inability of sufficient quantity of the energy molecule to bind to muscle; (2) this muscle problem reduces amount of air that can get in the lung and amount of oxygen carried in the blood, which then has the effect of increasing heart and respiration rates, blood pressure, and deep body temperature, and produces muscle rigidity; (3) the events noted above, when they occur during cardiac stress testing, are related to a problem similar to malignant hyperthermia (MH) reported in some muscle disorders without use of drugs known to cause MH. MH (a life-threatening metabolic reaction that classically is triggered when susceptible persons receive certain drugs used in anaesthesia.

Description:

This study is a research project initiated by the graduate research student (Mikaela I. Poling) and assisted by the clinical genetics fellow and graduate student (Andrés Morales) in partial fulfilment the requirements for their Masters degrees in Clinical and Applied Physiology, under approval, direction, and supervision of the study PI (Rodger J. McCormick).

Importance of Present Study:

FSS is a rare human neuromusculoskeletal disorder present before birth, involving primarily limb and craniofacial deformities. There are no prospective studies addressing physiological parameters, which are necessary to enable understanding of the underlying pathology and pathophysiology of Freeman-Sheldon syndrome. Elucidating any deviations in baseline and stress physiological parameters in FSS patients versus standard normal values and normal control subjects is of critical importance in tailoring therapeutic interventions to this challenging patient population.

Background:

Vanek et al. (1986) purposed FSS spectrum is a non-progressive congenital myopathy, giving pathological and electromyographical (EMG) evidence. They found white fibrose tissue within histologically normal muscle fibres, resulting in abnormal EMGs.

Toydemir et al. (2006) showed that mutations in embryonic myosin heavy chain 3 (MYH3), caused classic FSS phenotype, in which they screened 28 probands. In 20 patients, new missense mutations caused substitution of arginine at position 672 (arg672) by histidine or cytosine; arg672 is found in all myosin proteins post-embryonically. Of the remaining six patients in whom mutations were found, three had new missense or familial mutations; three other patients with sporadic expression had new, which were also found in Sheldon-Hall syndrome (SHS); two patients had no recognized mutations. They postulated these allelic variations at arg672 could affect adenosine triphosphate (ATP) binding. It is unknown how these mutations might correlate to the phenotypes observed. Their laboratory, including Stevenson et al. (2006) also presented strong evidence that FSS and SHS and similar distal arthrogryposes (DA) were distinct entities based on phenotype, natural history, and genotype.

Portillo et al. (unpublished data), in study of biopsies from their patient, found no evidence of muscle in the superior orbicularis oculi and found highly variable fibre size as a single pathological feature in a single vastus lateralis biopsy. Clinically, their patient, who had to-date the most severe expression of FSS, exhibited no function of the superior eyelid and reasonable muscle tone, bulk, and strength in the thigh. These findings suggested variable syndromic affectation by body region. They reported exertional dyspnea and resting tachycardia, without pathological features, in their patient and anecdotal information concerning exertional dyspnea in two other adult FSS patients. They also documented the occurrence of unexplained, seemingly stress-induced, episodic fever in their patient that resembled the malignant hyperthermia (MH) clinical triad of hyperthermia, tachycardia, and muscle rigidity.

In addition to age, gender, physical activity status, and concomitant disease and disability, maximal oxygen uptake, a function of exercise capacity, is genetically-controlled, and as already documented in other muscle disorders, the idiopathic febrile episodes reported by Portillo et al. may share physiological and biochemical similarities to the well-defined congenital muscle anomaly MH, which classically occurs when susceptible individuals receive inhaled anaesthetics, such as ether and halothane, or depolarizing muscle relaxants during surgery. Together, these clinical observations suggested there may be some syndromic relationship to exercise capacity and development of MH-like febrile syndrome, and it will be important to demonstrate these findings in a controlled experimental setting.

Significant differences among the similar distal arthrogryposes (DAs) may exist, with respect to the above, and this will be important to define experimentally, as well. Data concerning baseline and stress physiology in FSS and similar DAs could help to further define the distinct DA phenotypes clinically similar to FSS, contributing to nosological classification of FSS and related entities. This study will include FSS, Sheldon-Hall syndrome, DA type 1, and DA type 3.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: June 2022
• Est. primary completion date: June 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Syndrome Group Inclusion Criteria:

• Freeman-Sheldon syndrome,

• Sheldon-Hall syndrome,

• Distal arthrogryposis type 1, or

• Distal arthrogryposis type 3

• Deceased patients with enough clinical information available to satisfy study requirements

Syndrome Group Exclusion Criteria:

• Individuals not confirmed to have a condition under study

• Deceased patients without enough clinical information available to satisfy study requirements

• Patients with other anomalies, not having one of the above syndromes

• Patients or parents of minor children not willing to give consent

• Mature female patients who are pregnant or breast-feeding will be reassessed for consideration for enrolment.

• Mature female patients who are currently experiencing menses will be reassessed for consideration for enrolment.

• Patients with active, acute comorbid illness will be reassessed for consideration for enrolment.

Control Group Inclusion Criteria:

• Subjects must be healthy and free of active disease.

• Subject or parent of minor child must be willing to give consent.

• Subjects must fall within the age-bracket to be matched with a Syndrome Group patient already screened and enroled in the study

• Subjects must be non-tobacco users and non-drinkers.

Control Group Exclusion Criteria:

• Subjects exceptional for their age in body weight, stature, or habitus according to commonly accepted guidelines

• Subjects with active psychiatric illness, as manifested by abnormal mental status examination

• Subjects with active physical illness, especially respiratory or cardiac problem, as manifested by abnormal findings on physical examination

• Subjects with significant diagnosis of a constitutional disease or genetic disorder

• Subjects with a history of severe trauma resulting in either an anatomical of physiological deformity that impairs function

• Non-living subjects

• Candidates who fail the stress test

• Mature female subjects who are pregnant or breast-feeding will be reassessed for consideration for enrolment.

• Mature female subjects who are currently experiencing menses will be reassessed for consideration for enrolment.

• Subjects with active, acute illness will be reassessed for consideration for enrolment.

• Any other condition or anomaly expected to affect current physiology listed in AFI-48-123.

Related Conditions & MeSH terms

• Arthrogryposis
• Craniofacial Abnormalities

Intervention

Other:
• Lactate, Glucose, and Adenosine Triphosphate Blood Levels
Completed during the clinical examination and exercise test by the researchers, lactate, glucose, and free and total adenosine triphosphate blood levels are determined at rest and during exercise.

Procedure:
• Physiological Stress Test
During exercise, heart and lung function are monitored for changes caused by exercise, which increases the body's need for oxygen and puts extra demands on the heart. In this study, testing is done using a cycle ergometer and conducted according to the standardised exponential exercise protocol (STEEP).

Other:
• Functional Enquiry Form
Evaluated before clinical examination, it is a checklist of medical problems.
• Strength, Joint ROM, Girth and Length Measurements
Completed during the clinical examination by the researchers, it is a structured approach to evaluation of muscles, joints, arms, thighs, and legs.
• Study Physical Examination
Completed during the clinical examination by the researchers, it is a structured approach to a full physical examination (minus breasts, genitalia, or rectum).
• Observational Gait Analysis
Completed during the clinical examination by researchers, it is a structured approach to evaluation of a person's walking.
• Mental Health Interview
Completed during the clinical examination by the researchers, it is a general evaluation of mental health status.

Locations

Country	Name	City	State
United States	Freeman-Sheldon Research Group, Inc. Headquarters	Buckhannon	West Virginia

Sponsors (1)

Lead Sponsor	Collaborator
Freeman-Sheldon Research Group, Inc.

Country where clinical trial is conducted

United States, 

References & Publications (9)

Franklin B, Fern A, Fowler A, Spring T, Dejong A. Exercise physiologist's role in clinical practice. Br J Sports Med. 2009 Feb;43(2):93-8. doi: 10.1136/bjsm.2008.055202. Epub 2008 Dec 2. Review. — View Citation

Litman RS, Rosenberg H. Malignant hyperthermia: update on susceptibility testing. JAMA. 2005 Jun 15;293(23):2918-24. — View Citation

McCormick RJ. A Proposal for a Thesis: Heat Tolerance in Exercising Lean and Obese Middle-Aged Men. DEd diss., the Pennsylvania State University, 1973.

Myhill S, Booth NE, McLaren-Howard J. Chronic fatigue syndrome and mitochondrial dysfunction. Int J Clin Exp Med. 2009;2(1):1-16. Epub 2009 Jan 15. — View Citation

Northridge DB, Grant S, Ford I, Christie J, McLenachan J, Connelly D, McMurray J, Ray S, Henderson E, Dargie HJ. Novel exercise protocol suitable for use on a treadmill or a bicycle ergometer. Br Heart J. 1990 Nov;64(5):313-6. — View Citation

Portillo AL, Chamberlain RL, McCormick RJ, Poling MI. Histopathological and Operative Findings in a Severe Case of Freeman-Sheldon Syndrome: Implications for Nosology and Therapy. (Unpubl.) 2010.

Stevenson DA, Carey JC, Palumbos J, Rutherford A, Dolcourt J, Bamshad MJ. Clinical characteristics and natural history of Freeman-Sheldon syndrome. Pediatrics. 2006 Mar;117(3):754-62. — View Citation

Toydemir RM, Rutherford A, Whitby FG, Jorde LB, Carey JC, Bamshad MJ. Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome. Nat Genet. 2006 May;38(5):561-5. Epub 2006 Apr 16. — View Citation

Vanek J, Janda J, Amblerová V, Losan F. Freeman-Sheldon syndrome: a disorder of congenital myopathic origin? J Med Genet. 1986 Jun;23(3):231-6. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Body Composition	Body composition, measured by calliper, together with direct indices of physiological strain, is used to determined metabolic disease burden of Freeman-Sheldon syndrome and related conditions.	Evaluated before exercise, during two study visits (lasting an average of 1-3 hours)
Other	Hand Grip Strength	Decreased hand grip strength, measured by a hand dynamometer, is used as an index of physiological strain imposed by Freeman-Sheldon and related conditions	Evaluated during the first of two study visits
Primary	Heart rate	Increased heart rate, measured electrocardiographically, is used as an index of cardiovascular strain imposed by needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Primary	Oxygen Consumption	Oxygen consumption, measured by ventilation of expired oxygen, is used as a measure of physiological strain imposed by metabolic needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Non-Invasive Arterial Blood Pressure	Increased non-invasive arterial blood pressure rate is used as an index of cardiovascular strain imposed by needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Spirometry (Forced Expiratory Volume/Forced Vital Capacity)	Decreased ability of the lungs to move air, measured by forced expiration, is used as an index of strain imposed by Freeman-Sheldon syndrome and related conditions.	Evaluated before and after exercise, during two study visits (lasting an average of 1-3 hours)
Secondary	Saturation of Peripheral Oxygen	Decreased saturation of peripheral oxygen, measured by pulse oxymetry, is used as a measure of physiological strain imposed by metabolic needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Respiratory Rate	Increased respiratory rate, measured by plethysmograph, is used as a measure of physiological strain imposed by metabolic needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Heart Rhythm	Heart rhythms, monitored by electrocardiograph, are used as an index of cardiovascular strain imposed by needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Core Temperature	Increased core temperature, measured as oesophageal temperature, is used as a measure of physiological strain imposed by metabolic needs during exercise and exaggerated by Freeman-Sheldon, related conditions, and malignant hyperthermia.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Adenosine Triphosphate	Decreased adenosine triphosphate, measured as capillary blood level, is used as a measure of physiological strain imposed by metabolic needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Perceived Exertion	Increased perceived exertion, measured using the Borg scale, are used as an index of fatigue.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Muscle Rigidity	Increased muscle rigidity, evaluated by clinical examination and patient self-report, is used as an indicator of malignant hyperthermia, when increased core temperature, heart rate, and respiratory rate are present.	Evaluated while exercising, during second of two study visits (lasting an average of 1-3 hours)
Secondary	Functional and Health-Related Quality of Life	Functional and health-related quality of life, measured with the Medical Outcomes Trust Short Form (36) Health Survey (SF-36), is used as a general prediction of expected physical exercise capacity.	Evaluated in first of two study visits, lasting an average of 1-3 hours
Secondary	Lactic Acid	Lactic acid, measured by capillary blood level, is used as a measure of physiological strain imposed by metabolic needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)
Secondary	Glucose	Glucose, measured by capillary blood level, is used as an index of physiological strain, together with lactic acid and adenosine triphosphate capillary blood levels, imposed by metabolic needs during exercise and exaggerated by Freeman-Sheldon and related conditions.	Evaluated at rest and while exercising, during two study visits (lasting an average of 1-3 hours)

External Links

•   Freeman-Sheldon Research Group, Inc.: Organisational website. Includes organisation information and scientific and lay information on Freeman-Sheldon syndrome and related conditions.