Influence of prior pregnancies on disease course and cause of death in systemic sclerosis

被引:25
作者
Artlett, CM
Rasheed, M
Russo-Stieglitz, KE
Sawaya, HHB
Jimenez, SA
机构
[1] Thomas Jefferson Univ, Dept Med, Div Rheumatol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Jefferson Med Coll, Dept Obstet & Gynecol, Philadelphia, PA 19107 USA
关键词
D O I
10.1136/ard.61.4.346
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Microchimerism from fetal or maternal cells transferred during pregnancy has been implicated in the pathogenesis of systemic sclerosis (SSc). Objective: To determine whether a prior pregnancy influenced disease progression and cause of death in patients with SSc. Patients and methods: The patients comprised a retrospective study cohort of 111 women with SSc: 78 patients with prior pregnancies (PP) and 33 who were never pregnant (NP), followed up at Thomas Jefferson University. Differences in age at onset, disease subset, organ involvement, cause of death, and type of antinuclear autoantibodies were evaluated statistically, including regression analysis. Results: The age at onset of SSc in NP patients was 32.0 years compared with 45.7 years in patients with one or two prior pregnancies (p<0.0001), 46.6 years in patients with three or four pregnancies (p<0.0001), and 51.3 years in patients with five to seven pregnancies (p<0.0005). In the 16 patients who had an elective pregnancy termination, 14/16 (87.5%) had diffuse SSc v 2/16 (12.5%) with limited SSc (p<0.0001; odds ratio (OR)=49.0). Of the NP women, 7/30 (23%) died from SSc related causes v 3/78 (4%) women who had pregnancies (p=0.0058; OR=7.6). A carbon monoxide transfer factor (TLCO) of <60% and disease duration >10 years was found in 10/13 (77%) NP patients v 10/23 (43%) patients who had pregnancies (p=0.05; OR=4.7), and a TLCO <50% and disease duration > 10 years was identified in 7/13 (54%) NP patients v 6/23 (26%) of the patients who had pregnancies (p=0.09; OR=3.2). Conclusions: There are differences in the age at onset, clinical course, severity of lung involvement, and cause of death in women who develop SSc before pregnancy compared with those who develop it after pregnancies. The NP patients with SSc had onset of disease at an earlier age, more severe lung involvement, and higher rate of death due to SSc.
引用
收藏
页码:346 / 350
页数:5
相关论文
共 43 条
[21]   SCLERODERMA, SJOGREN-LIKE SYNDROME, AND CHRONIC GRAFT VERSUS HOST DISEASE [J].
LAWLEY, TJ ;
PECK, GL ;
MOUTSOPOULOS, HM ;
GRATWOHL, AA ;
DEISSEROTH, AB .
ANNALS OF INTERNAL MEDICINE, 1977, 87 (06) :707-709
[22]   Systemic sclerosis - A vascular perspective [J].
LeRoy, EC .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 1996, 22 (04) :675-&
[23]  
LEROY EC, 1988, J RHEUMATOL, V15, P202
[24]  
LIEGEOIS A, 1981, TRANSPLANT P, V13, P1250
[25]  
LIN H, 1993, J IMMUNOL, V151, P4562
[26]   Microchimerism of maternal origin persists into adult life [J].
Maloney, S ;
Smith, A ;
Furst, DE ;
Myerson, D ;
Rupert, K ;
Evans, PC ;
Nelson, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (01) :41-47
[27]  
MASI AT, 1980, ARTHRITIS RHEUM-US, V23, P875
[28]  
MULLINAX F, 1993, P 4 ASEAN C RHEUM, P30
[29]   Maternal-fetal immunology and autoimmune disease - Is some autoimmune disease auto-alloimmune or allo-autoimmune? [J].
Nelson, JL .
ARTHRITIS AND RHEUMATISM, 1996, 39 (02) :191-194
[30]  
Nelson JL, 1999, ARTHRITIS RHEUM, V42, pS277