TY - JOUR
T1 - Rheumatoid arthritis in a patient with compound heterozygous variants in the COL11A2 gene and progressive hearing loss
T2 - A case report
AU - Tsuchida, Yumi
AU - Nagafuchi, Yasuo
AU - Uehara, Tomoko
AU - Suzuki, Hisato
AU - Yamada, Mamiko
AU - Kono, Masanori
AU - Hatano, Hiroaki
AU - Shoda, Hirofumi
AU - Fujio, Keishi
AU - Kosaki, Kenjiro
N1 - Funding Information:
This work was supported by Research on Rare and Intractable Diseases from the Ministry of Health, Labour and Welfare, Japan, and the Initiative on Rare and Undiagnosed Diseases from the Japan Agency for Medical Research and Development.
Funding Information:
YT has received grants from GlaxoSmithKline. YN has received grants and/or speaking fees from BMS, Chugai, GlaxoSmithKline, Kissei, Mitsubishi Tanabe, and Pfizer. HS has received fees from Pfizer, Bristol-Myers Squibb, Eli Lilly, Sanofi, AbbVie, GlaxoSmithKline, Gulead, Boehringer Ingelheim, Jansen, Novartis, Chugai, Takeda, Astellas, Eisai, Asahi Kasei, and Daiichi-Sankyo, and has received research grants from Novartis. KF has received grants, consulting fees, speaking fees, and/or honoraria from Takeda, BMS, Mitsubishi Tanabe, Asahi Kasei, Sanofi, Eli Lilly, Daiichi-Sankyo, Ono, Janssen, AbbVie, Astellas, Eisai, Pfizer, Chugai, Novartis, UCB, Tsumura, Taisho Toyama, Nihon Kayaku, and Ayumi. All the other authors declared no conflicts of interest.
Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/2/18
Y1 - 2022/2/18
N2 - Rationale:Collagen type XI alpha 2 chain is a component of type XI collagen and is expressed in various tissues including articular cartilage and tectorial membrane of the cochlea. Variants in the COL11A2 gene, which encodes collagen type XI alpha 2 chain, has been reported to cause hearing loss and has been associated with osteoarthritis and ossification of the posterior longitudinal ligament of the spine. Despite the importance of type XI collagen in the joints, association of rheumatoid arthritis (RA) with COL11A2 has not been reported.Patient concerns:The patient is a 60-year-old female, born to Japanese parents of no known consanguinity. She had progressive hearing loss since childhood. Her father also had progressive hearing loss before middle age. She developed joint pain in the knees and the hips in her forties. When she was 56, she developed polyarthritis. Rheumatoid factor and anti-CCP antibodies were positive.Diagnoses:She was diagnosed with osteoarthritis and RA. Whole exome analysis detected 2 rare variants, c.4201C>T, p.(Arg1401Trp) and c4265C>T, p.(Pro1422Leu), in the COL11A2 gene (NM_080680.2). Whole genome analysis with a long insert size confirmed 2 variants that are in trans.Interventions and outcomes:She received a cochlear implant, which improved her hearing. She was treated with methotrexate, golimumab, tocilizumab, and upadacitinib with partial responses for her RA.Lessons:We herein report a patient with RA with compound heterozygous variants in the COL11A2 gene. Autoantibodies against type XI collagen are detected in the sera of patients with RA, suggesting the possibility that type XI collagen may be involved in the pathogenesis of RA as an autoantigen. The hearing loss and osteoarthritis in this patient may be due to the compound heterozygous variants in the COL11A2 gene, and the conformational changes induced by the variants may have changed the immunogenicity of type XI collagen, leading to the development of RA.
AB - Rationale:Collagen type XI alpha 2 chain is a component of type XI collagen and is expressed in various tissues including articular cartilage and tectorial membrane of the cochlea. Variants in the COL11A2 gene, which encodes collagen type XI alpha 2 chain, has been reported to cause hearing loss and has been associated with osteoarthritis and ossification of the posterior longitudinal ligament of the spine. Despite the importance of type XI collagen in the joints, association of rheumatoid arthritis (RA) with COL11A2 has not been reported.Patient concerns:The patient is a 60-year-old female, born to Japanese parents of no known consanguinity. She had progressive hearing loss since childhood. Her father also had progressive hearing loss before middle age. She developed joint pain in the knees and the hips in her forties. When she was 56, she developed polyarthritis. Rheumatoid factor and anti-CCP antibodies were positive.Diagnoses:She was diagnosed with osteoarthritis and RA. Whole exome analysis detected 2 rare variants, c.4201C>T, p.(Arg1401Trp) and c4265C>T, p.(Pro1422Leu), in the COL11A2 gene (NM_080680.2). Whole genome analysis with a long insert size confirmed 2 variants that are in trans.Interventions and outcomes:She received a cochlear implant, which improved her hearing. She was treated with methotrexate, golimumab, tocilizumab, and upadacitinib with partial responses for her RA.Lessons:We herein report a patient with RA with compound heterozygous variants in the COL11A2 gene. Autoantibodies against type XI collagen are detected in the sera of patients with RA, suggesting the possibility that type XI collagen may be involved in the pathogenesis of RA as an autoantigen. The hearing loss and osteoarthritis in this patient may be due to the compound heterozygous variants in the COL11A2 gene, and the conformational changes induced by the variants may have changed the immunogenicity of type XI collagen, leading to the development of RA.
KW - hearing loss
KW - osteoarthritis
KW - rheumatoid arthritis
KW - type XI collagen
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U2 - 10.1097/MD.0000000000028828
DO - 10.1097/MD.0000000000028828
M3 - Article
C2 - 35363175
AN - SCOPUS:85127437673
SN - 0025-7974
VL - 101
SP - E28828
JO - Medicine (United States)
JF - Medicine (United States)
IS - 7
ER -