Badowski Melissa E, Perez Sarah E
Department of Pharmacy Practice, Section of Infectious Diseases Pharmacotherapy, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
Infectious Diseases Clinic, Tufts Medical Center, Boston, MA, USA.
HIV AIDS (Auckl). 2016 Feb 10;8:37-45. doi: 10.2147/HIV.S81420. eCollection 2016.
Since the beginning of the HIV/AIDS epidemic, weight loss has been a common complaint for patients. The use of various definitions defining HIV wasting syndrome has made it difficult to determine its actual prevalence. Despite the use of highly active antiretroviral therapy, it is estimated that the prevalence of HIV wasting syndrome is between 14% and 38%. HIV wasting syndrome may stem from conditions affecting chewing, swallowing, or gastrointestinal motility, neurologic disease affecting food intake or the perception of hunger or ability to eat, psychiatric illness, food insecurity generated from psychosocial or economic concerns, or anorexia due to medications, malabsorption, infections, or tumors. Treatment of HIV wasting syndrome may be managed with appetite stimulants (megestrol acetate or dronabinol), anabolic agents (testosterone, testosterone analogs, or recombinant human growth hormone), or, rarely, cytokine production modulators (thalidomide). The goal of this review is to provide an in-depth evaluation based on existing clinical trials on the clinical utility of dronabinol in the treatment of weight loss associated with HIV/AIDS. Although total body weight gain varies with dronabinol use (-2.0 to 3.2 kg), dronabinol is a well-tolerated option to promote appetite stimulation. Further studies are needed with standardized definitions of HIV-associated weight loss and clinical outcomes, robust sample sizes, safety and efficacy data on chronic use of dronabinol beyond 52 weeks, and associated virologic and immunologic outcomes.
自艾滋病毒/艾滋病流行开始以来,体重减轻一直是患者常见的主诉。使用各种定义来界定艾滋病毒消瘦综合征,使得难以确定其实际患病率。尽管使用了高效抗逆转录病毒疗法,但据估计,艾滋病毒消瘦综合征的患病率在14%至38%之间。艾滋病毒消瘦综合征可能源于影响咀嚼、吞咽或胃肠蠕动的疾病,影响食物摄入或饥饿感或进食能力的神经疾病,精神疾病,心理社会或经济问题导致的食物无保障,或药物、吸收不良、感染或肿瘤引起的厌食症。艾滋病毒消瘦综合征的治疗可使用食欲刺激剂(甲地孕酮或屈大麻酚)、合成代谢剂(睾酮、睾酮类似物或重组人生长激素),或很少使用的细胞因子产生调节剂(沙利度胺)。本综述的目的是基于现有临床试验,对屈大麻酚治疗与艾滋病毒/艾滋病相关体重减轻的临床效用进行深入评估。尽管使用屈大麻酚后总体重增加有所不同(-2.0至3.2千克),但屈大麻酚是促进食欲刺激的耐受性良好的选择。需要进一步开展研究,对艾滋病毒相关体重减轻和临床结局进行标准化定义,确定足够大的样本量,获取屈大麻酚使用超过52周的长期安全性和疗效数据,以及相关的病毒学和免疫学结局。