Marjo Campmans-Kuijpers © ECCO |
Although Inflammatory Bowel Disease (IBD) has been historically associated with underweight and malnutrition, rates of obesity have been rising in patients with IBD, as in the general population. Nowadays, 15%–40% of adults with IBD are obese, and an additional 20%–40% are overweight [1]. Obesity is independently associated with higher disease burden and costs of hospitalisation in patients with IBD [2].
IBD may be an independent risk factor for development of obesity driven by dysbiosis and changes in the intestinal microbial metabolism [3,4]. Recent evidence implies that changes in the intestinal immune system contribute to metabolic disease [3]. Furthermore, in patients with IBD, serum levels of adiponectin, resistin, and active ghrelin are increased, whereas serum levels of leptin are decreased [4]. In addition, drug treatment used for IBD, in particular corticosteroids and anti-tumour necrosis factor alpha (TNF) therapies, may also increase obesity [1]. Conversely, obesity is associated with changes to the gut microbiota and intestinal barrier function and predisposes to altered intestinal immunity [2,4], and metabolically active adipose tissue might contribute to a pro-inflammatory susceptibility to IBD [3].
Existing data on the impact of obesity on IBD susceptibility and disease course are, however, inconsistent. One study in IBD patients found obesity not to be significantly associated with the odds of achieving clinical remission, clinical response or mucosal healing during either induction or maintenance therapy [5]. Pharmacokinetic studies of several anti-TNF agents in patients with immune-mediated inflammatory diseases have demonstrated accelerated drug clearance with increasing body weight [6–8], and this is probably also true in IBD [9]. A recent study showed a high body mass index (BMI) to be independently associated with an increased risk of treatment failure and surgery in biologic-treated patients with Ulcerative Colitis (UC) [10]. This inconsistency in data may explained by the fact that most studies use only BMI to measure adiposity.
BMI is unable to distinguish between lean body mass and other tissues. Therefore, sarcopenia (low lean mass) is difficult to detect. Current data on sarcopenia in IBD are scarce due to retrospective study designs and inappropriate functional assessment [11]. Sarcopenia has been associated with an increased need for surgery and poor surgical outcomes in IBD, as well as with osteopenia [12–14], and it has been found to be a significant (p=0.002) predictor of need for surgery in overweight and obese subjects [2].
Furthermore, different adiposity compartments have distinct metabolic profiles [12]. In many patients with Crohn’s Disease (CD), visceral adipose tissue is increased [12] and it has been reported that increased visceral to subcutaneous fat ratio is associated with a higher postoperative inflammatory response (higher procalcitonin levels) in IBD patients undergoing colorectal resection [15]. In addition, patients with CD (but not those with UC) have a unique form of visceral adipose tissue, mesenteric fat hyperplasia (“creeping fat”), that is limited to areas of inflamed bowel [16]. This mesenteric fat increases C-reactive protein and may contribute to systemic obesity.
A recent study found that the increasing rates of obesity in patients with IBD coincide with decreases in lean muscle mass over time, while high rates of osteopenia remain stable [17]. Therefore, better assessment of body composition and studies on fat deposition in IBD patients are urgently needed to guide therapy on both sarcopenia and pro-inflammatory fat depositions.