SMA CARNI-VAL TRIAL PART II: A Prospective, Single-Armed Trial of L-Carnitine and Valproic Acid in Ambulatory Children with Spinal Muscular Atrophy

被引:88
作者
Kissel, John T. [1 ,2 ]
Scott, Charles B. [3 ]
Reyna, Sandra P. [4 ]
Crawford, Thomas O. [6 ,7 ]
Simard, Louise R. [8 ]
Krosschell, Kristin J. [9 ]
Acsadi, Gyula [10 ,11 ]
Elsheik, Bakri [1 ,2 ]
Schroth, Mary K. [12 ]
D'Anjou, Guy [13 ]
LaSalle, Bernard [14 ]
Prior, Thomas W. [15 ]
Sorenson, Susan [16 ]
Maczulski, Jo Anne [17 ]
Bromberg, Mark B. [4 ]
Chan, Gary M.
Swoboda, Kathryn J. [4 ,5 ]
机构
[1] Ohio State Univ, Dept Neurol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Pediat, Columbus, OH 43210 USA
[3] CBS Squared Inc, Ft Washington, PA USA
[4] Univ Utah, Sch Med, Dept Neurol, Salt Lake City, UT USA
[5] Univ Utah, Sch Med, Dept Pediat, Salt Lake City, UT USA
[6] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[7] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
[8] Univ Manitoba, Dept Biochem & Med Genet, Winnipeg, MB, Canada
[9] Northwestern Univ, Dept Phys Therapy & Human Movement Sci, Feinberg Sch Med, Chicago, IL 60611 USA
[10] Wayne State Univ, Sch Med, Dept Neurol, Detroit, MI 48201 USA
[11] Wayne State Univ, Sch Med, Dept Pediat, Detroit, MI 48201 USA
[12] Univ Wisconsin, Sch Med, Dept Pediat, Madison, WI USA
[13] Hop St Justine, Div Pediat Neurol, Montreal, PQ H3T 1C5, Canada
[14] Univ Utah, Sch Med, Dept Biomed Informat, Salt Lake City, UT USA
[15] Ohio State Univ, Dept Mol Pathol, Columbus, OH 43210 USA
[16] Primary Childrens Med Ctr, Salt Lake City, UT 84103 USA
[17] Pediat Occupat Therapy Serv, Chicago, IL USA
基金
美国国家卫生研究院;
关键词
HAND-HELD DYNAMOMETRY; SMN2 COPY NUMBER; PROTEIN-LEVEL; MODEL MICE; SURVIVAL; GENE; PHENOTYPE; IDENTIFICATION; INCREASES; SEVERITY;
D O I
10.1371/journal.pone.0021296
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Multiple lines of evidence have suggested that valproic acid (VPA) might benefit patients with spinal muscular atrophy (SMA). The SMA CARNIVAL TRIAL was a two part prospective trial to evaluate oral VPA and l-carnitine in SMA children. Part 1 targeted non-ambulatory children ages 2-8 in a 12 month cross over design. We report here Part 2, a twelve month prospective, open-label trial of VPA and L-carnitine in ambulatory SMA children. Methods: This study involved 33 genetically proven type 3 SMA subjects ages 3-17 years. Subjects underwent two baseline assessments over 4-6 weeks and then were placed on VPA and L-carnitine for 12 months. Assessments were performed at baseline, 3, 6 and 12 months. Primary outcomes included safety, adverse events and the change at 6 and 12 months in motor function assessed using the Modified Hammersmith Functional Motor Scale Extend (MHFMS-Extend), timed motor tests and fine motor modules. Secondary outcomes included changes in ulnar compound muscle action potential amplitudes (CMAP), handheld dynamometry, pulmonary function, and Pediatric Quality of Life Inventory scores. Results: Twenty-eight subjects completed the study. VPA and carnitine were generally well tolerated. Although adverse events occurred in 85% of subjects, they were usually mild and transient. Weight gain of 20% above body weight occurred in 17% of subjects. There was no significant change in any primary outcome at six or 12 months. Some pulmonary function measures showed improvement at one year as expected with normal growth. CMAP significantly improved suggesting a modest biologic effect not clinically meaningful. Conclusions: This study, coupled with the CARNIVAL Part 1 study, indicate that VPA is not effective in improving strength or function in SMA children. The outcomes used in this study are feasible and reliable, and can be employed in future trials in SMA.
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页数:11
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