Keywords
CAPN3
- muscular dystrophy - LGMDR1 - next-generation sequencing
Introduction
Calpainopathy caused by mutations in the CAPN3 gene (OMIM:114240) is one of the most common types of autosomal recessive limb-girdle
muscular dystrophy (ARLGMD). The disease onset ranges from early childhood to adulthood
and is typically characterized by progressive symmetrical weakness and wasting of
proximal limb muscles and contractures.[1 ] While the recessive form of LGMD (LGMDR1) is the most common one, the autosomal
dominant form (LGMDD4) of calpainopathy has been reported in few families with adult
onset and milder phenotypes.[2 ]
[3 ]
CAPN3 gene encodes a protease called calpain3 and is located in the chromosome region 15q15.1–q21.1.[4 ]
CAPN3 is a Ca2+ dependent protein comprising of 821 amino acids.[5 ]
[6 ] The gene consists of 24 exons and produces a skeletal muscle-specific homodimer
cysteine protease belonging to the calpain superfamily which is involved in myofibrillogenesis
and sarcomere remodeling.[7 ]
[8 ]
[9 ]
[10 ] The prevalence of calpainopathy among all dominant and recessive forms of LGMD's
ranges from 11% in the United States and Mexico,[11 ]
[12 ]
[13 ] to 40 to 50% in Turkey, India, and Bulgaria,[14 ]
[15 ]
[16 ]
[17 ] and even higher in Basque and Russia population.[18 ]
[19 ]
[20 ]
Although a few reports based on western blot confirmation of calpainopathy are published
on Indian patients,[21 ]
[22 ] only two studies describe the mutation pattern in the Indian community with calpainopathy
and none on the disease progression.[23 ]
[24 ] Additionally, a few international studies from Italy and France reported on the
natural history/disease progression.[25 ]
[26 ]
[27 ]
In the current study, we elaborated on the clinical presentation, disease progression,
and mutation pattern of a large cohort of genetically confirmed LGMDR1 patients evaluated
at a single quaternary referral center for neurological disorders in India. Since
we will be discussing only the recessive form, the term “LGMDR1” will be used synonymously
with “calpainopathy.”
Materials and Methods
Institutional ethics committee approval for the study was obtained (NIMHANS/IEC/2020–21).
This is a retrospective analysis with a description of the clinical phenotype and
mutation pattern in 72 patients of genetically confirmed LGMDR1 patients. They belonged
to a cohort of 345 ARLGMD patients evaluated between 2016 and 2020 at the multidisciplinary
neuromuscular disorders clinic. After detailed history taking and neurological examination
of all patients, relevant demographic and clinical data were entered in SPSS (Statistical
Package for the Social Sciences) for further statistical analysis. It is commonly
used for analysis of complex statistical data. The muscle strength was evaluated by
the modified Medical Research Council (MRC) grading scale[28 ] which is an objective method used clinically to assess individual muscle weakness.
After obtaining written informed consent, patients underwent genetic testing by next-generation
sequencing (NGS) including clinical exome or whole exome sequencing. The libraries
were sequenced on the Illumina sequencing platform, followed by bioinformatic analysis
customized for calling single nucleotide variants (SNVs), small insertion/deletions
(INDELs), as well as larger copy number variants (CNVs; exon deletions and duplications).
CAPN 3 variant annotation was done based on GenBank transcript: NM_000070.3. We used the
free version of VarSome online tool (
https://www.varsome.com/
) and manual application of American College of Medical Genetics and Genomics (ACMG)
criteria (2015)[29 ] for classification of SNVs and INDELs. CNVs when identified were automatically considered
as causing loss of function and classified as pathogenic. Multiplex ligation-dependent
probe amplification (MLPA) was also performed in two patients with large multiexon
deletions identified by NGS.
We checked available data in Clinvar, Human Gene Mutation Database (HGMD), Leiden
variant database (
https://databases.lovd.nl/shared/genes/CAPN3
), and literature for identification of reported variants. Demographic and phenotype
data of patients were entered in SPSS Version 23 for statistical analysis. To study
the disease progression with respect to time to loss of independent ambulation and
time to wheel chair and bed bound state, all the details were obtained from the medical
records. A simple questionnaire with information for functional and physical disability
was posted to all genetically confirmed LGMDR1 patients to collect their latest disability
status.
Statistics
Data were analyzed in SPSS version 23 using descriptive statistics, such as mean and
standard deviation for continuous variables. Frequency percentage was used for categorical
variables. Comparison between two genotype groups was performed by independent sample
t -test. The significance level (p -value) was fixed at 0.05.
Results
Among the 345 genetically confirmed ARLGMD patients, we identified 72 LGMDR1 (20.9%)
individuals from 72 independent families. The mean age at onset was 13.5 ± 6.4 (range:
1–35) years, and the mean duration was 6.3 ± 4.7 (range: 0.4–20) years. There were
34 (47.2%) males. Patients from the southern states of India formed 75.4% of the study
cohort, followed by 17.8% from the Eastern states, while the remaining (6.9%) were
from the West and Northern parts. Consanguinity was reported in 39 (54.2%) patients,
and a family history of similar illness was present in 17 (23.3%). About 29 (40.3%)
patients had onset before 12 years of age, while 35 (48.6%) had onset between 12 and
20 years of age, and only 8 (11.1%) had onset after 20 years. The initial symptoms
were progressive proximal lower limb weakness (52.1%), toe walking (20.5%), and difficulty
running fast (9.6%), while a small proportion (5.5%) had a combination of these at
the onset. The clinical features are summarized in [Table 1 ].
Table 1
Clinical profile of 72 patients of calpainopathy
Parameter
Total number(n = 72)
Percentage
Duration of illness (y)
6.3 ± 4.7
Male:female
34:38
Consanguinity
39
54.2
Family history
17
23.3
Initial symptom
Age of onset (y)
13.5 ± 6.4
Proximal lower limb weakness
38
52.1
Toe walking
15
20.5
Difficulty in running fast
7
9.6
Combination of symptoms
4
5.5
Repeated falls
4
5.5
Muscle pain
2
2.8
Calf swelling
1
1.4
Delayed motor milestones
1
1.4
Symptoms at presentation
Difficulty in climbing stairs
70
97.2
Difficulty in getting up
70
97.2
Proximal upper limb weakness
48
66.6
Running difficulty
41
56.9
Recurrent falls
36
50
Muscle pain
12
16.6
Exercise intolerance
9
12.5
Distal upper limb weakness
6
8.3
Distal lower limb weakness
2
2.7
Examination
Scapular winging
50
69.4
Contractures
42
58.3
Toe walking
29
40.2
Lumbar lordosis
28
38.8
Calf hypertrophy
24
33.3
At presentation, 70 (97.2%) patients had difficulty in rising from the floor and climbing
stairs from mean ages of 14.5 ± 6.1 and 14.9 ± 5.8 years, respectively. Recurrent
falls were reported by 36 (50%) patients from a mean age of 15.6 ± 6.0 years. About
48 (66.6%) patients presented with proximal upper limb weakness from 16.7 ± 5.7 years
of age, and a small proportion of 6 (8.3%) patients had features of distal upper limb
weakness with later onset at the age of 17.7 ± 4.8 years. About 41 (56.9%) patients
had observed that they had difficulty in running like others from a mean age of 14.7 ± 6.8
years. Other presentations were muscle pain and exercise intolerance in 12 (16.6%)
and 9 (12.5%) patients, respectively. Two (2.7%) were in wheelchair/bedbound state
at 18 and 26 years of age with 11 and 14 years into their illness, respectively. None
of the patients had symptoms to suggest cranial muscle involvement.
On examination, approximately 28 (38.8%) had prominent lumbar lordosis, 24 (33.3%)
had mild calf hypertrophy, and 13 (18.1%) patients had prominent atrophy of calves
and arms. Scapular winging was noticed in 50 (69.4%) and prominent contractures in
42 (58.3%) patients, predominantly at the ankles and knees. Around 15 (20.8%) patients
had mild facial weakness. The muscle strength was severely reduced in the girdle muscles
([Fig. 1 ]). Preferential involvement of the muscles was recorded: pectoralis and biceps muscles
were more severely involved than deltoids and triceps. Iliopsoas, hip adductors, and
gastrocnemius were more affected than the glutei and anterior leg muscles. The pattern
of muscle involvement is summarized in [Table 2 ]. Distal muscles were preserved in the majority of patients ([Fig. 1 ]). All individuals had a waddling gait associated with prominent toe walking in 29
(40.3%). Tendon reflexes were generally hypoactive but ankle jerk was preserved in
52 (72.2%) patients.
Fig. 1 Severity of various muscle weakness among 72 patients with “calpainopathy.”
Table 2
Muscle selectivity pattern in calpainopathy patients
Selectivity pattern
Number
Percentage
Upper limbs
Deltoid > pectoralis
8
10.9
Deltoid = pectoralis
25
35.6
Deltoid < pectoralis
39
53.4
Arm
Biceps > triceps
36
50.6
Biceps = triceps
29
39.7
Biceps < triceps
7
9.5
Lower limbs
Iliopsoas > gluteus maximus
15
20.5
Iliopsoas = gluteus maximus
26
35.6
Iliopsoas < gluteus maximus
31
43.8
Thigh
Adductors > abductors
49
67.1
Adductors = abductors
19
27.4
Adductors < abductors
4
5.5
Leg
Gastrocnemius > tib anterior
4
5.5
Gastrocnemius = tib anterior
51
69.9
Gastrocnemius < tib anterior
17
24.7
Genetic Findings
Among the 72 genetically confirmed LGMDR1 patients, 57 had homozygous and the remaining
15 had compound heterozygous mutations in the CAPN3 gene. Among the compound heterozygous cases, all except two had missense variant
in one allele with suspected loss of function variant like frameshift causing INDEL
or splice affecting intronic substitution in the opposite allele. Two compound heterozygous
patients had biallelic INDELs and missense variants, respectively (Pt_20 and Pt_28).
Out of 57 homozygous cases, 29 had missense variants, 28 had suspected loss of function
variants (splice affecting intronic variants = 13; INDELs causing frameshift = 10;
multiexonic deletions = 3; inframe 3 bp deletion = 1; and substitution resulting in
nonsense codon = 1). In total, 47 unique disease-causing CAPN3 variants were identified in this study, out of which 19 are novel mutations ([Fig. 2 ]; [Supplementary Table S1 ], available in online version only).
Fig. 2 Schematic representation of the variations identified in our study in CAPN3 gene with corresponding exons and protein domains. The 24 exons of CAPN3 (NM_000070.3) are represented as boxes with respective exonic numbers with noncoding
regions shaded in black and gray at the ends. The domain information is based on UniProtKB
- P20807 (CAN3_HUMAN) taken from Uniprot database (
https://www.uniprot.org/
). The novel variants are underlined. The dark dots represent homozygous variations,
unfilled dots represent heterozygous variations, semifilled dot represent compound
heterozygous variations. Triangles represent missense, squares represent frameshift,
rhombus represent nonsense and hexagon represent intronic variations. ; @, +, - Individuals
carry two homozygous variations in CAPN3 . The size of exons /introns is not represented at scale. Calpain catalytic domain
and EF-hand domains 1–4 are shown in red.
While disease causing variants are scattered across the CAPN3 gene with no specific hotspot regions, we identified few recurrent variants in Indian
patients ([Table 4 ]). The commonest mutation identified are c.2051–1G > T and c.2338G > C in seven (9.7%)
patients each. Other mutation clusters were c.802–9G > A, c.1319G > A, and c.1343G > A
occurring in five (6.9%) patients each, while c.1963delC was identified in four (5.5%)
patients. Exon 10 was most frequently involved in our patients with 12 mutations (16.7%).
No mutations were observed in exons 2, 3, 7, and 12. Large deletions were observed
between exons 17 to 24 in three unrelated patients by NGS. We confirmed the deletion
in two of the three patients with additional deletion/duplication analysis by MLPA.
The family members of 31 patients were screened by segregation analysis and at least
one member was found to be having a heterozygous state, and six members with similar
illness were detected to have homozygous status ([Supplementary Table S2 ], available in online version only).
Genotypic Patterns and Disease Progression
Clinical follow-up details were available in 55 (76.4%) patients with a mean duration
of 4.5 ± 4.3 years. About 92.7% of them were ambulant at a mean age of 23.7 ± 7.6
years, while the remaining 7.3% (four patients) had become wheelchair bound at a mean
age of 25.5 ± 5.7 years, after 13.5 (13.5 ± 4.6) years into the illness. On subgroup
analysis among patients with different mutations, those with missense mutations had
later age of presentation and slow disease progression than those with other mutations
([Table 3 ]). Among patients in wheelchair-bound state, only one had missense mutation (Pt_64).
Three patients (4.1%) were available for follow-up with age more than 40 years and
disease duration ranging from 5 to 20 years (Pt_26, Pt_36, and Pt_39); all were ambulant
with assistance of which two were having missense mutations. The oldest patient with
follow-up in our study cohort is 43 years, with 20 years of illness duration (Pt_26).
One patient (Pt_17) with splice affecting mutation (c.802–9G > A) had sudden death
at 21 years of age after 7 years into the illness and was reported to be due to cardiac
arrest; however, medical records are not available. None of the patients had features
suggestive of respiratory distress during the period of clinical follow-up.
Table 3
Genotypic correlation among calpainopathy patients with clinical follow-up (n = 55)
Parameters
Group 1: n = 24 (missense mutation)
Group 2: n = 31 (other mutations)
p -Value
Age of onset (y)
16.4 ± 7.0
11.7 ± 5.66
0.07
Duration (y)
6.4 ± 4.4
6.4 ± 5.3
0.9
Age at presentation (y)
22.8 ± 7.1
18.13 ± 7.0
0.02
Male:female
12:12
12:19
NA
Consanguinity (yes:no)
14:10
17:14
NA
Presence of family history
8
5
NA
Mean age of follow-up (y)
25.4 ± 7.5
22.2 ± 8.3
0.14
Wheelchair bound status during follow-up
1
3
NA
Abbreviation: NA, not applicable.
Discussion
In the current study, we present the results of clinical findings, pattern of disease
progression, and genetic mutation profile of a large number of LGMDR1 patients from
India. The majority of them belong to southern India and demonstrated varied mutation
patterns. In an earlier study from India, LGMDR1 is reported to be the commonest form
of ARLGMD; however, there is no clear data about the exact prevalence and subtypes
of genetically confirmed patients.[14 ] In our study, LGMDR1 constituted 21.2% of all genetically confirmed ARLGMD patients.
The age of onset of muscle weakness in the present study is in concordance with previous
studies[20 ]
[22 ]; however, a later age of onset has been noted in a study from Japan.[30 ] Both genders were equally affected in our study, similar to the findings in other
large series.[31 ]
[32 ] However, in one study from India with 75 patients, male predominance was noted.[14 ]
Nearly half of our patients had proximal weakness of lower limbs as the initial presentation
and almost 20% had tip-toe walking. Scapular winging was noted in 69% of patients.
The commonest presentation described in other studies are similar with difficulty
in running, tip-toe walking, and scapular winging along with proximal lower limb weakness.[25 ]
[32 ]
[33 ] In a study by Peric et al, from Serbia, up to 74% of their patients had features
of proximal lower limb weakness as the initial presentation, and scapular winging
was noticed in more than two-thirds of their patients.[34 ]
The pectorals, biceps brachii, and gluteus maximus were the weakest muscles. This
pattern of selective involvement is also reported in a previous study.[35 ] The symmetrical and preferential muscle involvement also helps in identifying the
clinical phenotype which could aid in precise genetic testing.[36 ]
[37 ]
In the course of disease progression, upper limb weakness was noted in about two-thirds
of patients by 3 years of symptom onset and had limb-girdle weakness as was seen in
our previous study.[22 ] However, in one study from north India, only 16% of them had this feature, and this
could be due to the varied time of evaluation after disease onset in these patients.[14 ]
The mean duration of follow-up and mean age at last follow-up were 4.5 and 23.7 years,
respectively. The majority of our patients continued to be ambulant at a mean of 10
years after the onset of symptoms suggesting a relatively benign course of the illness.
In one of the largest studies by Sáenz et al, among 238 LGMDR1 patients, the mean
age at becoming wheel chair dependent was 32.2 years, approximately 18 years after
the mean age of disease onset.[32 ] In a study from Italy, Angelini et al have documented loss of ambulation from 10
to 30 years after disease onset,[25 ] similar to the study from the United Kingdom, where loss of ambulation occurred
at 35.2 years, that is, approximately 22.6 years after onset of symptoms.[38 ] Similar observations were noted in other European reports.[27 ]
[32 ] Hence, further long-term follow-up of our patients is necessary for assessing the
future status of disease progression. In one of our patients with sudden death at
21 years of age, it was suspected to be due to myocardial infarction. In the previous
studies, though respiratory insufficiency is frequently observed in calpainopathy
patients, a few cases of cardiac involvement are also reported.[39 ]
Mutation analysis in our cohort has shown 47 different mutations, and the spectrum
is distributed throughout the length of the CAPN3 gene ([Fig. 2 ]). The majority of mutations are of missense type. Even previous studies have described
34 to 60% of mutations of missense type, and exons 10 and 21 were more susceptible
than exons 2, 3, 7, and 12.[24 ]
[33 ]
The mutational changes in exon 10, that is, c.1343G > A, and c.1319G > A, leading
to missense variation and amino acid substitution occurred in 13.8% of our population.
This accumulation and gene pooling in our study cohort could be contributed by consanguinity
which is more prevalent in southern India. Overall, 550 delA is the commonest among
the Caucasian population with founder effect being demonstrated in Mediterranean and
southern European region.[40 ] However, this mutation was not found in our current Indian cohort. Founder mutations
seen in the Brazilian population, R110X, and 2362—2363EG4TCATCT was also not identified
in our study.[41 ] Nevertheless, one founder variant (c.2306G > A) in exon 22, previously described
in Amish community of northern Indiana of the United States was detected in one of
our patients.[4 ] Another variant previously described in La reunion island of Indian ocean (c.946–2A > G)
was also detected in our series.[35 ]
Seven mutations seen in previously described mutational “hotspot” of exon 21, constituted
only approximately 6.9% in our study population.[41 ] As the types of genetic mutations are known to vary from region to region and with
ethnic background, the distribution of CAPN3 mutations in this study did not show any clear hot spots except for mutation accumulation
in exon 10 in 12 cases. We also did not observe any mutations in exons 2, 3, 7, and
12. This wide range of mutations observed in our study could also be due to heterogeneous
population of patients with a wide range of ethnicity. In another study from a north
Indian center, exon 16 was the commonest mutation site, and approximately 75.6% of
mutation groups were located around nine exons.[24 ] This further strengthens the wide variation of genetic mutation from various regions
within India.
There were two patients in the current cohort (Pt_10 and Pt_11) carrying two homozygous
variations in CAPN3 at exon4/11 c.529G > T/c.1448C > T. Both had onset of symptoms at 15 and 18 years,
respectively, with features of proximal lower limb weakness with one (Pt_11) having
muscle pain as additional symptom. Though both were from different families, they
belonged to a single community and during the follow-up duration of 6 years each,
both were still ambulant. Both these novel mutations, c.529G > T/c.1448C > T in these
patients were likely pathogenic based on ACMG classification suggesting their role
in the clinical phenotype. Large exonic deletions are uncommon in CAPN3 but deletions from exons 2 to 8 have been described before.[17 ] In our study, large deletions were observed in three unrelated patients. Interestingly,
all belong to the Patel community which is believed to originate and be more prevalent
in Gujarat. The Agarwal founder mutations: c.2051–1G > T and c.2338G > C were the
most recurrent ones in our cohort occurring in total eight patients (compound heterozygous:
6 and homozygous: 2), all belonging to the Agarwal community as described before[23 ] ([Table 4 ]; [Supplementary Table S1 ], available in online version only). There was no direct correlation observed between
the type of genetic mutation and course of disease progression, except those with
missense mutation had a more benign course of disease progression than those with
nonmissense mutations. However, observation about intrafamilial mutation pattern and
disease progression could not be done.
Table 4
Recurrent CAPN3 variants in our cohort
Variants
Number of patients
Patient ID
Location
Zygosity
c.2051–1G > T
7 (9.7%)
Pt_52 to 58
Intron18
Heterozygous
c.2338G > C(p.Asp780His)
7 (9.7%)
Pt_52 to 58
Exon 22
Heterozygous
c.802–9G > A
5 (6.9%)
Pt_15 to Pt_19
Intron 5
Homozygous
c.1319G > A(p.Arg440Gln)
5 (6.9%)
Pt_24 to Pt_28
Exon 10
Homozygous
c.1343G > A(p.Arg448His)
5 (6.9%)
Pt_30 to Pt_34
Exon 10
Homozygous
c.1963delC
4 (5.5%)
Pt_45 to 48
Exon 17
Homozygous
c.145C > T(p.Arg49Cys)
2 (2.7%)
Pt_1, Pt_2
Exon 1
Homozygous
c.304C > T(p.Pro102Ser)
2 (2.7%)
Pt_3, Pt_4
Exon 1
Homozygous
c.529G > T(p.Val177Phe)[a ]
2 (2.7%)
Pt_10, Pt_11
Exon 4
Homozygous
c.1448C > T(p.Ala483Val)[a ]
2 (2.7%)
Pt_10, Pt_11
Exon 11
Homozygous
c.1743dupT(p.Glu582T)
2 (2.7%)
Pt_38, Pt_39
Exon 13
Homozygous
c.1782 + 1G > A[a ]
2 (2.7%)
Pt_42, Pt_43
Exon 17
Homozygous
a Novel variants.
The current study is one of the largest series describing the clinical phenotype,
disease progression, and mutation patterns in genetically confirmed LGMDR1 and the
first from south India. This study also shows the segregation of CAPN 3 mutation in first-order relatives of the family ([Supplementary Table S2 ], available in online version only). This study also highlights mutation clusters
around few exons, aiding in the diagnosis in limited settings.
Limitations
Major limitations of this study are that although it has identified genetic mutation
clusters, a still larger sample size from each community needs to be screened for
these mutations to look for founder effect in this region. Studying intrafamilial
genetic variability with phenotypic assessment will further help in understanding
this disease pattern. No longitudinal follow-up was performed to investigate the disease
progression and natural history.
Conclusion
Hereby, we describe the genetic mutation pattern of CAPN 3 gene and disease progression in Indian, predominantly south Indian patients of LGMDR1.
Most of the patients develop symptoms in the second decade with proximal lower limb
weakness. The predominant findings include abnormal gait with scapula winging. The
majority of the patients remained ambulant even after 10 years of symptoms onset,
suggesting a benign course of illness. There were 47 different mutations noted in
these patients with 19 novel variants. These novel variants identified in CAPN3 expand the genotype–phenotype correlation associated with LGMDR1 in Indian population.
Our study brings into light the usefulness of NGS for identifying novel variants in
LGMDR1 and can be used as a stand-alone molecular diagnostic screening tool for all
LGMD-related genes. However, additional confirmation might be required for larger
deletions/duplications and complex rearrangements.
