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1.
Arthritis Rheum ; 41(9): 1689-94, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9751103

ABSTRACT

OBJECTIVE: Because former investigations have reported abnormal changes in the expression of serotonin (5-hydroxytryptamine [5-HT]) and substance P (SP) in serum and cerebrospinal fluid, this study sought to determine whether 5-HT and pain-modulating neuropeptides (SP, galanin [GA], pituitary adenylyl cyclase-activating polypeptide, and secretoneurin) were expressed abnormally in the muscle tissue of patients with fibromyalgia (FM). METHODS: Snap-frozen muscle tissue specimens (deltoid muscles) from 10 patients with FM (mean disease duration 15 years) and from 10 healthy control subjects were examined by reverse transcriptase-polymerase chain reaction (RT-PCR) of RNA preparations from muscle cells, and by immunohistochemistry methods (alkaline phosphatase-anti-alkaline phosphatase and immunogold-silver) using specific primers as well as antibodies. When specific messenger RNA (mRNA) was detected by RT-PCR, in situ RT-PCR was performed for mRNA localization. RESULTS: Specific mRNA for the examined substances was absent in 9 of 10 FM patients and in 10 of 10 controls. No differences between the FM patients and controls could be detected in the muscle tissue by immunohistochemistry. In 1 FM patient, mRNA for the GA receptor could be shown. CONCLUSION: This study showed that 5-HT and neuropeptides are not produced in the muscle of patients with FM, and therefore do not appear to be involved in the peripheral induction of pain in this chronic, painful disorder.


Subject(s)
Fibromyalgia/metabolism , Muscle, Skeletal/metabolism , Neuropeptides/metabolism , Serotonin/metabolism , Adult , Aged , DNA Primers/chemistry , Female , Galanin/genetics , Galanin/metabolism , Humans , Immunoenzyme Techniques , Male , Middle Aged , Neuropeptides/genetics , Pituitary Adenylate Cyclase-Activating Polypeptide , Polymerase Chain Reaction , RNA, Messenger/biosynthesis , Secretogranin II , Serotonin/genetics , Substance P/genetics , Substance P/metabolism
4.
Am J Med Genet ; 65(1): 44-51, 1996 Oct 02.
Article in English | MEDLINE | ID: mdl-8914740

ABSTRACT

To delineate further the clinical spectrum of Menkes disease, an X-linked recessive disorder of copper transport, we studied 4 related males, ranging in age from 4-38 years, with a unique phenotype that combines manifestations of classical and mild Menkes disease and occipital horn syndrome (OHS). The propositus, and 18-year-old man, was evaluated following an intracerebral hemorrhage at age 15 years and was noted to have marked hypotonia, motor delay with mental retardation, bladder diverticula, failure to thrive, and diarrhea from infancy; seizures from age 3 years; and abnormal hair (pili torti) and face, cutis laxa, and multiple joint dislocations. Radiographic abnormalities included occipital exostoses, tortuous cerebral blood vessels with multiple branch occlusions, and hammer-shaped clavicles. Biochemical studies demonstrated reduced copper and ceruloplasmin levels in serum, and abnormal plasma catecholamine ratios. We reported previously the molecular defect in this family, a splice-site mutation that predicts formation of approximately 20% of the normal Menkes gene product [Kaler et al., 1994: Nat Genet 18:195-202]. Here, we detail the clinical course and physical features and radiographic findings in these 4 individuals, and compare their phenotype with classical and mild Menkes and OHS. Unusual Menkes disease variants such as this may escape recognition due to anomalies that appear inconsistent with the diagnosis, particularly prolonged survival and later onset of seizures. Males with mental retardation and connective tissue abnormalities should be evaluated for biochemical evidence of defective copper transport.


Subject(s)
Ehlers-Danlos Syndrome/physiopathology , Menkes Kinky Hair Syndrome/physiopathology , Adolescent , Adult , Child , Child, Preschool , Ehlers-Danlos Syndrome/diagnostic imaging , Ehlers-Danlos Syndrome/genetics , Exostoses/diagnostic imaging , Humans , Infant , Male , Menkes Kinky Hair Syndrome/diagnostic imaging , Menkes Kinky Hair Syndrome/genetics , Occipital Bone/diagnostic imaging , Pedigree , Phenotype , Radiography
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